The Human Obesity Gene Map: The 2005 Update

Cites (1,346)

Items 201–400 of 1,346

1. Mutations in the protein kinase A R1α regulatory subunit cause familial cardiac myxomas and Carney complex
   Mairead Casey, Carl J. Vaughan, Jie He, Cathy J. Hatcher, Jordan Michael Winter, Stanislawa Weremowicz, Kate T. Montgomery, Raju Kucherlapati, Cynthia Casson Morton, Craig T. Basson · 2000 · Journal of Clinical Investigation
2. MECP2 is highly mutated in X-linked mental retardation
   Philippe Couvert · 2001 · Human Molecular Genetics
3. Imprinting-Mutation Mechanisms in Prader-Willi Syndrome
   Tohru Ohta, Todd A. Gray, Peter K. Rogan, Karin Buiting, James M. Gabriel, Shinji Saitoh, Bethi Muralidhar, B. Bilienska, Małgorzata Krajewska‐Walasek, Daniel J. Driscoll et al. · 1999 · The American Journal of Human Genetics
4. Congenital Leptin Deficiency Due to Homozygosity for the Δ133G Mutation: Report of Another Case and Evaluation of Response to Four Years of Leptin Therapy
   Gibson, William T., Farooqi, I. Sadaf, Moreau, Mary, DePaoli, Alex M., Lawrence, Elizabeth, O’Rahilly, Stephen, Trussell, Rebecca A. · 2004 · The Journal of Clinical Endocrinology & Metabolism
5. Targeted Disruption of the Tumor Necrosis Factor-α Gene: Metabolic Consequences in Obese and Nonobese Mice
   John R. Ventre, Thomas W. Doebber, Margaret S. Wu, Karen L. MacNaul, Karla A. Stevens, Manolis Pasparakis, George A. Kollias, David E. Moller · 1997 · Diabetes
6. Mutations in MKKS cause Bardet-Biedl syndrome
   Anne Michele Slavotinek, Edwin M. Stone, Kirk Mykytyn, John R. Heckenlively, Jane S. Green, Elise Héon, Maria A. Musarella, Patrick S. Parfrey, Val C. Sheffield, Leslie G. Biesecker · 2000 · Nature Genetics
7. Identification of the gene that, when mutated, causes the human obesity syndrome BBS4
   Kirk Mykytyn, Terry A. Braun, Rivka Carmi, Neena B. Haider, Charles C. Searby, Mythreyi Shastri, Gretel E. Beck, Alan F. Wright, Alessandro Iannaccone, Khalil Elbedour et al. · 2001 · Nature Genetics
8. Mutational and Haplotype Analyses of Families with Familial Partial Lipodystrophy (Dunnigan Variety) Reveal Recurrent Missense Mutations in the Globular C-Terminal Domain of Lamin A/C
   Rebecca A. Speckman, Abhimanyu Garg, Fenghe Du, Lynda B. Bennett, Rose A. Veile, Elif A Oral, Simeon I. Taylor, Michael Lovett, Anne M. Bowcock · 2000 · The American Journal of Human Genetics
9. Detection of quantitative trait loci for growth and fatness in pigs
   Jean Pierre Bidanel, Denis Milan, Nathalie Iannuccelli et al. · 2001 · Genetics Selection Evolution
10. Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)
    Darryl Y. Nishimura · 2001 · Human Molecular Genetics
11. A potential link between muscle peroxisome proliferator- activated receptor-α signaling and obesity-related diabetes
    Finck, Brian N., Bernal-Mizrachi, Carlos, Han, Dong Ho, Coleman, Trey, Sambandam, Nandakumar, LaRiviere, Lori L., Holloszy, John O., Semenkovich, Clay F., Kelly, Daniel P. · 2005 · Cell Metabolism
12. Androgen Receptor Null Male Mice Develop Late-Onset Obesity Caused by Decreased Energy Expenditure and Lipolytic Activity but Show Normal Insulin Sensitivity With High Adiponectin Secretion
    Fan, WuQiang, Yanase, Toshihiko, Nomura, Masatoshi, Okabe, Taijiro, Goto, Kiminobu, Sato, Takashi, Kawano, Hirotaka, Kato, Shigeaki, Nawata, Hajime · 2005 · Diabetes
13. A Novel Heterozygous Mutation in Peroxisome Proliferator-Activated Receptor-γ Gene in a Patient with Familial Partial Lipodystrophy
    Anil K. Agarwal, Abhimanyu Garg · 2002 · The Journal of Clinical Endocrinology & Metabolism
14. Polymorphisms of the 5-HT2C receptor and leptin genes are associated with antipsychotic drug-induced weight gain in Caucasian subjects with a first-episode psychosis
    Lucy A. Templeman, Gavin P. Reynolds, Belén Arranz, Luis San · 2005 · Pharmacogenetics and Genomics
15. Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis.
    Lee Scott Weinstein, Pablo V. Gejman, Eitan Friedman · 1990 · Proceedings of the National Academy of Sciences
16. Paradoxical resistance to diet-induced obesity in UCP1-deficient mice
    Xiaotuan Liu, Martin Rossmeisl, Jennifer W. McClaine, Leslie P. Kozak · 2003 · Journal of Clinical Investigation
17. Genetic Interaction of BBS1 Mutations with Alleles at Other BBS Loci Can Result in Non-Mendelian Bardet-Biedl Syndrome
    Philip L. Beales, José Luis Badano, Alison J. Ross, Stephen J. Ansley, Bethan E. Hoskins, Brigitta Kirsten, Charles A. Mein, Philippe Froguel, Peter James Scambler, Richard Alan Lewis et al. · 2003 · The American Journal of Human Genetics
18. Inhibition of adipogenesis and development of glucose intolerance by soluble preadipocyte factor–1 (Pref-1)
    Kichoon Lee, Josep A. Villena, Yang Soo Moon, Kee‐Hong Kim, Sun‐Joo Lee, Chulho Kang, Hei Sook Sul · 2003 · Journal of Clinical Investigation
19. Development of Cushing's syndrome in corticotropin-releasing factor transgenic mice
    Mary P. Stenzel‐Poore, Vicky A. Cameron, Joan M. Vaughan, Paul E. Sawchenko, Wylie Vale · 1992 · Endocrinology
20. Neuronal Shp2 tyrosine phosphatase controls energy balance and metabolism
    Eric Erquan Zhang, Emilie A. Chapeau, Kazuki Hagihara, Gen‐Sheng Feng · 2004 · Proceedings of the National Academy of Sciences
21. PPARG F388L, a Transactivation-Deficient Mutant, in Familial Partial Lipodystrophy
    Robert Alexander Hegele, Henian Cao, Christy Frankowski, Suresh T. Mathews, Todd Leff · 2002 · Diabetes
22. The Q223R Polymorphism of the Leptin Receptor Gene Is Significantly Associated with Obesity and Predicts a Small Percentage of Body Weight and Body Composition Variability
    Nikos Yiannakouris, Mary Yannakoulia, Labros Melistas, Jean Lin Chan, Dorothy J. Klimis‐Zacas, Christos Socrates Mantzoros · 2001 · The Journal of Clinical Endocrinology & Metabolism
23. Association of the INS VNTR with size at birth
    David B. Dunger, Ken K. Ong, Stewart J. Huxtable, Andrea Sherriff, Kathryn A. Woods, M. Lynn Ahmed, Jean Golding, Marcus E Pembrey, Susan M. Ring, the ALSPAC Study Team et al. · 1998 · Nature Genetics
24. Inactivation of the hepatic cytochrome P450 system by conditional deletion of hepatic cytochrome P450 reductase
    Henderson, Colin J., Otto, Diana M.E., Carrie, Dianne, Magnuson, Mark A., McLaren, Aileen W., Rosewell, Ian, Wolf, C. Roland · 2003 · Journal of Biological Chemistry
25. Normal plasma lipoproteins and fertility in gene-targeted mice homozygous for a disruption in the gene encoding very low density lipoprotein receptor.
    Frykman, P K, Brown, M S, Yamamoto, T, Goldstein, J L, Herz, J · 1995 · Proceedings of the National Academy of Sciences
26. Progressive Adipocyte Hypertrophy in Aquaporin-7-deficient Mice
    Mariko Hara‐Chikuma, Eisei Sohara, Tatemitsu Rai · 2005 · Journal of Biological Chemistry
27. Absence of the lipid phosphatase SHIP2 confers resistance to dietary obesity
    Mark W. Sleeman, Katherine E. Wortley, Ka‐Man Venus Lai, Lori C. Gowen, Jennifer Kintner, William O. Kline, Karen García, Trevor N. Stitt, George D. Yancopoulos, Stanley J. Wiegand et al. · 2005 · Nature Medicine
28. Genetic Determinants of Energy Expenditure and Insulin Resistance in Diet-Induced Obesity in Mice
    Katrine Almind, C. Ronald Kahn · 2004 · Diabetes
29. Cytosolic NADP+-dependent Isocitrate Dehydrogenase Plays a Key Role in Lipid Metabolism
    Ho‐Jin Koh, Su‐Min Lee, Byung-Gap Son, Soh-Hyun Lee, Zae Young Ryoo, Kyu‐Tae Chang, Jeen‐Woo Park, Dong‐Chan Park, Byoung Joon Song, Richard L. Veech et al. · 2004 · Journal of Biological Chemistry
30. Adipocyte-Specific Glucocorticoid Inactivation Protects Against Diet-Induced Obesity
    Erin E. Kershaw, Nicholas M. Morton, Harveen Dhillon, Lynne E. Ramage, Jonathan R. Seckl, Jeffrey S. Flier · 2005 · Diabetes
31. Genetic analysis of non-insulin dependent diabetes mellitus in the GK rat
    Joakim Galli, Luo-Sheng Li, Anna Glaser, Claes‐Göran Östenson, Hong Jiao, Hossein Fakhrai-Rad, Howard J. Jacob, Eric S. Lander, Holger Luthman · 1996 · Nature Genetics
32. Detection of Obesity QTLs on Mouse Chromosomes 1 and 7 by Selective DNA Pooling
    Benjamin A. Taylor, Sandra J. Phillips · 1996 · Genomics
33. Hypertension in mice lacking the proatrial natriuretic peptide convertase corin
    Joyce C. Y. Chan, Ole Knudson, Faye Y. Wu · 2005 · Proceedings of the National Academy of Sciences
34. A Glucocorticoid Receptor Gene Marker Is Associated with Abdominal Obesity, Leptin, and Dysregulation of the Hypothalamic‐Pituitary‐Adrenal Axis
    Roland Rosmond, Yvon C. Chagnon, Göran Holm, Monique Chagnon, Louis Përusse, Kajsa Lindell, Björn Carlsson, Claude Bouchard, Per A Björntorp · 2000 · Obesity Research
35. The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region
    Philippe Jay, Claire Rougeulle, Annick Massacrier, Anne Moncla, Marie‐Geneviève Mattéi, Perrine Malzac, Nathalie Roëckel, Sylvie A. Taviaux, Jean‐Louis Bergé‐Lefranc, Pierre Cau et al. · 1997 · Nature Genetics
36. Phenotypic and Genetic Heterogeneity in Congenital Generalized Lipodystrophy
    Anil K. Agarwal, Vinaya Simha, Elif A Oral, Stephanie Ann Moran, Phillip Görden, Stephen O’Rahilly, Zohra Zaidi, Figen Gürakan, Silva A Arslanian, Aharon Klar et al. · 2003 · The Journal of Clinical Endocrinology & Metabolism
37. Identification of a novel paternally expressed gene in the Prader - Willi syndrome region
    Rachel Wevrick, Julie A. Kerns, Uta Francke · 1994 · Human Molecular Genetics
38. Mutations in the human melanocortin-4 receptor gene associated with severe familial obesity disrupts receptor function through multiple molecular mechanisms
    Giles S.H. Yeo · 2003 · Human Molecular Genetics
39. Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder.
    Nicholas Katsanis, SJ Ansley, JL Badano, ER Eichers, Lewis Ra, Beth Hoskins, Peter James Scambler, W. S. Davidson, Philip L. Beales, Lupski · 2002 · UCL Discovery (University College London)
40. Insulin receptor substrate 2 plays a crucial role in β cells and the hypothalamus
    Kubota, Naoto, Terauchi, Yasuo, Tobe, Kazuyuki, Yano, Wataru, Suzuki, Ryo, Ueki, Kohjiro, Takamoto, Iseki, Satoh, Hidemi, Maki, Toshiyuki, Kubota, Tetsuya et al. · 2004 · Journal of Clinical Investigation
41. Adipose-specific overexpression of GLUT4 reverses insulin resistance and diabetes in mice lacking GLUT4 selectively in muscle
    Eugénia Carvalho, Ko Kotani, Odile D. Peroni, Barbara B. Kahn · 2005 · American Journal of Physiology-Endocrinology and Metabolism
42. The Adipose Tissue Phenotype of Hormone‐Sensitive Lipase Deficiency in Mice
    Shu Pei Wang, Nancy Laurin, Jean Himms‐Hagen, Michael A. Rudnicki, Emile H. Levy, Marie‐France Robert, Linghe Pan, Luc Laurier Oligny, Grant A. Mitchell · 2001 · Obesity Research
43. Postembryonic ablation of AgRP neurons in mice leads to a lean, hypophagic phenotype
    Gavin A. Bewick, James Gardiner, Waljit Singh Dhillo, Aysha S. Kent, Nicholas E. White, Zoë Webster, Mohammad A. Ghatei, Stephen Robert Bloom · 2005 · The FASEB Journal
44. A molecular genome scan analysis to identify chromosomal regions influencing economic traits in the pig. II. Meat and muscle composition
    Massoud Malek, Jack C. M. Dekkers, Hakkyo K. Lee · 2001 · Mammalian Genome
45. Genome Scan for Human Obesity and Linkage to Markers in 20q13
    Joseph Hyungwoo Lee, Danielle R. Reed, Weidong Li, Weizhen Xu, Eun-Jeong Joo, Robin L. Kilker, Elizabeth J. Nanthakumar, Michael A. North, H. Sakul, Callum J. Bell et al. · 1999 · The American Journal of Human Genetics
46. Identification of an obesity quantitative trait locus on mouse chromosome 2 and evidence of linkage to body fat and insulin on the human homologous region 20q.
    A. V. Lembertas, Louis Përusse, Yvon C. Chagnon, Janis S. Fisler, Craig H. Warden, Deborah A. Purcell-huynh, France T. Dionne, Jacques Gagnon, André Nadeau, Aldons Jake Lusis et al. · 1997 · Journal of Clinical Investigation
47. A Whole-Genome Scan for Obstructive Sleep Apnea and Obesity
    Lyle John Palmer, Sarah G. Buxbaum, Emma K. Larkin, Sanjay R. Patel, Robert C. Elston, Peter V. Tishler, Susan S Redline · 2003 · The American Journal of Human Genetics
48. Comparative Genomic Analysis Identifies an ADP-Ribosylation Factor–like Gene as the Cause of Bardet-Biedl Syndrome (BBS3)
    Annie Pei-Fen Chiang, Darryl Y. Nishimura, Charles C. Searby, Khalil Elbedour, Rivka Carmi, Amanda L. Ferguson, J.L. Secrist, Terry A. Braun, Thomas L. Casavant, Edwin M. Stone et al. · 2004 · The American Journal of Human Genetics
49. IL-1 Plays an Important Role in Lipid Metabolism by Regulating Insulin Levels under Physiological Conditions
    Taizo Matsuki, Reiko Horai, Katsuko Sudo, Yoichiro Iwakura · 2003 · The Journal of Experimental Medicine
50. Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutations
    Cécile Lubrano-Berthelier · 2003 · Human Molecular Genetics
51. A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader–Willi syndrome critical region
    Jong, M. T. C., Gray, T. A., Ji, Y., Glenn, C. C., Saitoh, S., Driscoll, D. J., Nicholls, R. D. · 1999 · Human Molecular Genetics
52. Two Polymorphisms in the Peroxisome Proliferator-Activated Receptor- Gene Are Associated with Severe Overweight among Obese Women
    Raisa Valve, Katariina Sivenius, Raija Miettinen, Jussi Pihlajamäki, A Rissanen, S S Deeb, Johan H. Auwerx, Matti I.J. Uusitupa, Markku Laakso · 1999 · The Journal of Clinical Endocrinology & Metabolism
53. Overexpression of Sterol Regulatory Element-binding Protein-1a in Mouse Adipose Tissue Produces Adipocyte Hypertrophy, Increased Fatty Acid Secretion, and Fatty Liver
    Jay D. Horton, Iichiro Shimomura, Shinji Ikemoto, Yuriy K. Bashmakov, Robert E. Hammer · 2003 · Journal of Biological Chemistry
54. Familial Dwarfism due to a Novel Mutation of the Growth Hormone-Releasing Hormone Receptor Gene 1
    Roberto Salvatori, C Y Hayashida, Manuel Herminio Aguiar-Oliveira, John A. Phillips, Anita H. O. Souza, Rogério G. Gondo, Sergio P. A. Toledo, Maria M. Conceicão, Melissa Prince, Hiralal Maheshwari et al. · 1999 · The Journal of Clinical Endocrinology & Metabolism
55. Polymorphisms of the tumour necrosis factor‐α gene, coronary heart disease and obesity
    Herrmann, Ricard, Nicaud, Mallet, Arveiler, Evans, Ruidavets, Luc, Bara, Parra et al. · 1998 · European Journal of Clinical Investigation
56. Defective fatty acid uptake modulates insulin responsiveness and metabolic responses to diet in CD36-null mice
    Tahar Hajri, Xiao Xia Han, Arend Bonen, Nada A. Abumrad · 2002 · Journal of Clinical Investigation
57. The TNF-α Gene Neo I Polymorphism Influences the Relationship Among Insulin Resistance, Percent Body Fat, and Increased Serum Leptin Levels
    José Manuel Fernández‐Real, Cristina Gutiérrez, Wifredo Ricart, Roser Casamitjana, M Fernández-Castañer, Joan Josep Vendrell, Cristóbal Richart, Joan Soler · 1997 · Diabetes
58. SPARC-null mice exhibit increased adiposity without significant differences in overall body weight
    Amy D. Bradshaw, D. C. Graves, Kouros Motamed · 2003 · Proceedings of the National Academy of Sciences
59. Identification of SH2-B as a key regulator of leptin sensitivity, energy balance, and body weight in mice
    Decheng Ren, Minghua Li, Chaojun Duan, Liangyou Rui · 2005 · Cell Metabolism
60. Linkage Between Markers in the Vicinity of the Uncoupling Protein 2 Gene and Resting Metabolic Rate in Humans
    Claude Bouchard, Louis Përusse, Yvon C. Chagnon, Craig H. Warden, Daniel Ricquier · 1997 · Human Molecular Genetics
61. Role of the Fatty Acid Binding Protein mal1 in Obesity and Insulin Resistance
    Kazuhisa Maeda, K. Teoman Uysal, Liza Makowski, Cem Z. Görgün, Gen‐ichi Atsumi, Rex A. Parker, Jens C. Brüning, Ann Vogel Hertzel, David Bernlohr, Gökhan S. Hotamışlıgil · 2003 · Diabetes
62. Targeted Deletion of the Vgf Gene Indicates that the Encoded Secretory Peptide Precursor Plays a Novel Role in the Regulation of Energy Balance
    Seung Hahm, Tooru M. Mizuno, T. John Wu, Jonathan P. Wisor, Catherine A. Priest, Christine A. Kozak, Carol N. Boozer, Bonnie W. Peng, Robert C. McEvoy, Paul Good et al. · 1999 · Neuron
63. In vivo modulation of Hmgic reduces obesity
    Ashim Anand, Kiran K. Chada · 2000 · Nature Genetics
64. Identification of a Novel Bardet-Biedl Syndrome Protein, BBS7, That Shares Structural Features with BBS1 and BBS2
    José Luis Badano, Stephen J. Ansley, Carmen C. Leitch, Richard Alan Lewis, James R. Lupski, Nicholas Katsanis · 2003 · The American Journal of Human Genetics
65. A Polymorphism in the Leptin Promoter Region (-2548 G/A) Influences Gene Expression and Adipose Tissue Secretion of Leptin
    J. Hoffstedt, Per Olof Eriksson, Salim Mottagui‐Tabar, Peter Arner · 2002 · Hormone and Metabolic Research
66. The Human Obesity Gene Map: The 2002 Update
    Yvon C. Chagnon, Tuomo Rankinen, Eric E. Snyder, S. John Weisnagel, Louis Përusse, Claude Bouchard · 2003 · Obesity Research
67. Identification of polymorphic loci in the promoter region of the serotonin 5-HT 2C receptor gene and their association with obesity and Type II diabetes
    Xiaohong Yuan, Kentaro Yamada, Satomi Ishiyama-Shigemoto · 2000 · Diabetologia
68. Normal hemostasis but defective hematopoietic response to growth factors in mice deficient in phospholipid scramblase 1
    Quansheng Zhou, Ji Zhao, Therese Wiedmer, Peter Jay Sims · 2002 · Blood
69. Angiopoietin-related growth factor antagonizes obesity and insulin resistance
    Yuichi Oike, Masaki Akao, Kunio Yasunaga, Toshimasa Yamauchi, Tohru Morisada, Yasuhiro Ito, Takashi Urano, Yoshishige Kimura, Yoshiaki Kubota, Hiromitsu Maekawa et al. · 2005 · Nature Medicine
70. Obesity and mild hyperinsulinemia found in neuropeptide Y-Y1 receptor-deficient mice
    Atsuko Kushi, Hitoshi Sasai, Haruko Koizumi, Noriko Takeda, Masahiro Yokoyama, Motonao Nakamura · 1998 · Proceedings of the National Academy of Sciences
71. Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping
    Val C. Sheffield, Rivka Carml, Anne E. Kwitek, Tatiana Rokhlina, Darryl Nishlmura, Geoffrey M. Duyk, Khalil Elbedour, Sara L.F. Sunden, Edwin M. Stone · 1994 · Human Molecular Genetics
72. Melanocortin-4 Receptor Gene Variant I103 Is Negatively Associated with Obesity
    Frank Geller, Kathrin Reichwald, Astrid Dempfle, Thomas Illig, Caren Vollmert, Stephan Herpertz, Winfried Siffert, Matthias Platzer, Claudia Hess, Thomas W. Gudermann et al. · 2004 · The American Journal of Human Genetics
73. A Mutation in the β3-Adrenergic Receptor Gene Is Associated with Obesity and Hyperinsulinemia in Japanese Subjects
    H. Kadowaki, Koichiro Yasuda, K Iwamoto et al. · 1995 · Biochemical and Biophysical Research Communications
74. Mutations in PHF6 are associated with Börjeson–Forssman –Lehmann syndrome
    Karen M. Lower, GILLIAN M. TURNER, Bronwyn A. Kerr, Katherine D. Mathews, Marie A Shaw, Ági K. Gedeon, Susan L. Schelley, H. Eugene Hoyme, Susan M. White, Martin Bruce Delatycki et al. · 2002 · Nature Genetics
75. Liver-specific Deletion of the NADPH-Cytochrome P450 Reductase Gene
    Gu, Jun, Weng, Yan, Zhang, Qing-Yu, Cui, Huadong, Behr, Melissa, Wu, Lin, Yang, Weizhu, Zhang, Li, Ding, Xinxin · 2003 · Journal of Biological Chemistry
76. Association of Polymorphisms at the SR-BI Gene Locus With Plasma Lipid Levels and Body Mass Index in a White Population
    Susan L. Acton, Doreen P. Osgood, Mary Donoghue, Dolores Corella, Miguel Pocovı́, Ana Cenarro, Pilar Mozas, John Keilty, Sharon L. Squazzo, Elizabeth A. Woolf et al. · 1999 · Arteriosclerosis Thrombosis and Vascular Biology
77. Identification of a Novel Genetic Locus for Familial Cardiac Myxomas and Carney Complex
    Mairead Casey, Caroline S. Mah, Andrew D. Merliss, Lawrence Steven Kirschner, Susan E. Taymans, Alfred E. Denio, Bruce R. Korf, Alan David Irvine, Anne E. Hughes, J. Aidan Carney et al. · 1998 · Circulation
78. RAPID COMMUNICATIONS: Mutations in the Preproghrelin/Ghrelin Gene Associated with Obesity in Humans
    Olavi H. Ukkola, Éric Ravussin, Peter Jacobson, Eric E. Snyder, Monique Chagnon, Lars Sjöström, Claude Bouchard · 2001 · The Journal of Clinical Endocrinology & Metabolism
79. Transgenic Expression of Syndecan-1 Uncovers a Physiological Control of Feeding Behavior by Syndecan-3
    Ofer Reizes, John M. Lincecum, Zihua Wang, Olga Goldberger, Li Huang, Marko Kaksonen, Rexford S. Ahima, Michael T. Hinkes, Gregory S. Barsh, Heikki Rauvala et al. · 2001 · Cell
80. Genetic dissection of atypical antipsychotic-induced weight gain: novel preliminary data on the pharmacogenetic puzzle.
    Vincenzo Santo Basile, Mario Masellis, Roger S. McIntyre, Herbert Y. Meltzer, Jeffrey Alan Lieberman, James L. Kennedy · 2001 · PubMed
81. Pancreatic β-Cell Failure and Diabetes in Mice With a Deletion Mutation of the Endoplasmic Reticulum Molecular Chaperone Gene P58IPK
    Warren Ladiges, Sue E. Knoblaugh, John Morton, Marcus J. Korth, Bryce L. Sopher, Carole R. Baskin, A MacAuley, Alan G. Goodman, Renee C. LeBoeuf, Michael G. Katze · 2005 · Diabetes
82. Neuromedin U has a novel anorexigenic effect independent of the leptin signaling pathway
    Reiko Hanada, Hitoshi Teranishi, James T. Pearson, Mamoru Kurokawa, Hiroshi Hosoda, Nobuhiro Fukushima, Yoshihiko Fukue, Ryota Serino, Hiroaki Fujihara, Yoichi Ueta et al. · 2004 · Nature Medicine
83. APOE ε4 is associated with obstructive sleep apnea/hypopnea
    D. J. Gottlieb, Anita L. DeStefano, Dan Foley, Emmanuel Jean-Marie Mignot, Susan S Redline, Rachel J. Givelber, Terry B Young · 2004 · Neurology
84. Deletion of the Angiotensin Type 2 Receptor (AT2R) Reduces Adipose Cell Size and Protects From Diet-Induced Obesity and Insulin Resistance
    Laurent Yvan‐Charvet, Patrick C. Even, May Bloch-Faure, Michèle Guerre-Millo, Naïma Moustaïd‐Moussa, Pascal Ferré, Annie Quignard‐Boulangé · 2005 · Diabetes
85. Melanocortin-4 Receptor Gene: Case-Control Study and Transmission Disequilibrium Test Confirm that Functionally Relevant Mutations Are Compatible with a Major Gene Effect for Extreme Obesity
    Anke Hinney, Sarah Hohmann, Frank Geller, CONSTANZE VOGEL, Claudia Hess, Anne‐Kathrin Wermter, Britta Brokamp, Hanspeter Goldschmidt, Wolfgang Siegfried, Helmut Remschmidt et al. · 2003 · The Journal of Clinical Endocrinology & Metabolism
86. A genetic polymorphism of the peroxisome proliferator-activated receptor gamma gene influences plasma leptin levels in obese humans
    Aline Meirhaeghe · 1998 · Human Molecular Genetics
87. Increased glucose metabolism and insulin sensitivity in transgenic skinny mice overexpressing leptin.
    Yoshihiro Ogawa, Hiroaki Masuzaki, Kiminori Hosoda, Megumi Aizawa‐Abe, Junko Suga, M Suda, Ken Ebihara, H Iwai, N Matsuoka, Noriko Satoh et al. · 1999 · Diabetes
88. Lipin Expression Preceding Peroxisome Proliferator-activated Receptor-γ Is Critical for Adipogenesis in Vivo and in Vitro
    Jack Phan, Miklós Péterfy, Karen Reue · 2004 · Journal of Biological Chemistry
89. The impact of the CYP2D6 polymorphism on haloperidol pharmacokinetics and on the outcome of haloperidol treatment
    Jürgen Brockmöller, Julia Kirchheiner, Jürgen Schmider, Silke Walter, Christoph Sachse, Bruno Müller-Oerlinghausen, Ivar Roots · 2002 · Clinical Pharmacology & Therapeutics
90. Estrogen Deficiency, Obesity, and Skeletal Abnormalities in Follicle-Stimulating Hormone Receptor Knockout (FORKO) Female Mice**This investigation was supported in part by the Canadian Institutes of Health Research.
    Natalia Danilovich, P. Suresh Babu, Weirong Xing, Maria Gerdes, Hanumanthappa Krishnamurthy, M. Ram Sairam · 2000 · Endocrinology
91. Involvement of Hypothalamic Histamine H1 Receptor in the Regulation of Feeding Rhythm and Obesity
    Takayuki Masaki, Seiichi Chiba, Tohru Yasuda, Hitoshi Noguchi, Tetsuya Kakuma, Takeshi Watanabe, Toshiie Sakata, Hironobu Yoshimatsu · 2004 · Diabetes
92. Effects of mutations in the human uncoupling protein 3 gene on the respiratory quotient and fat oxidation in severe obesity and type 2 diabetes.
    George A. Argyropoulos, Angela M. Brown, Steven Matthew Willi, Ju Zhu, Y He, Marc L. Reitman, Sahr M. Gevao, Ida J. Spruill, William Timothy Garvey · 1998 · Journal of Clinical Investigation
93. Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndrome
    Deborah L. Stone, Anne Michele Slavotinek, Gerard G. Bouffard, Sharmila Banerjee‐Basu, Andreas D. Baxevanis, Mason Barr, Leslie G. Biesecker · 2000 · Nature Genetics
94. A Gender-specific Role For Phosphatidylethanolamine N-Methyltransferase-derived Phosphatidylcholine in the Regulation of Plasma High Density and Very Low Density Lipoproteins in Mice
    Anna A. Noga, Dennis E. Vance · 2003 · Journal of Biological Chemistry
95. Factors of Insulin Resistance Syndrome–Related Phenotypes Are Linked to Genetic Locations on Chromosomes 6 and 7 in Nondiabetic Mexican-Americans
    Rector Arya, John Blangero, Ken Williams, Laura A. Almasy, Thomas D. Dyer, Robin J. Leach, Peter O'Connell, Michael P. Stern M. D, Ravindranath Duggirala · 2002 · Diabetes
96. Accelerated Fat Absorption in Intestinal Alkaline Phosphatase Knockout Mice
    Sonoko Narisawa, Lei Huang, Arata Iwasaki, Hideaki Hasegawa, David Alpers, José Luís Millán · 2003 · Molecular and Cellular Biology
97. Difference in obesity phenotype between orexin-knockout mice and orexin neuron-deficient mice with same genetic background and environmental conditions
    Junko Hara, Masashi Yanagisawa, Takeshi Sakurai · 2005 · Neuroscience Letters
98. Mitochondrial Glycerol-3-Phosphate Acyltransferase-Deficient Mice Have Reduced Weight and Liver Triacylglycerol Content and Altered Glycerolipid Fatty Acid Composition
    Linda E. Hammond, Patricia A. Gallagher, Shuli Wang, Sylvia Hiller, Kimberly D. Kluckman, E. L. Posey-Marcos, Nobuyo Maeda, Rosalind Coleman · 2002 · Molecular and Cellular Biology
99. Polymorphism of the Promoter Region of the Serotonin 5-HT2C Receptor Gene and Clozapine-Induced Weight Gain
    Gavin P. Reynolds, Zhijun Zhang, Xiaobin Zhang · 2003 · American Journal of Psychiatry
100. A New Clinical Condition Linked to a Novel Mutation in Lamins A and C with Generalized Lipoatrophy, Insulin-Resistant Diabetes, Disseminated Leukomelanodermic Papules, Liver Steatosis, and Cardiomyopathy
     Frédéric A. Caux, Emmanuelle Dubosclard, Olivier Lascols, Brigitte Buendia, Olivier Chazouillères, Ariel A. Cohen, Jean‐Claude Courvalin, Liliane Laroche, Jacqueline Capeau, Corinne Vigouroux et al. · 2003 · The Journal of Clinical Endocrinology & Metabolism
101. Mutational analysis of melanocortin-4 receptor, agouti-related protein, and α-melanocyte-stimulating hormone genes in severely obese children
     Béatrice Dubern, Karine Clément, Véronique Pelloux, Philippe Froguel, J.-P. Girardet, Bernard Guy-grand, Patrick Tounian · 2001 · The Journal of Pediatrics
102. Association of the Pro12Ala Polymorphism in the PPAR-γ2 Gene With 3-Year Incidence of Type 2 Diabetes and Body Weight Change in the Finnish Diabetes Prevention Study
     Virpi Lindi, Matti I.J. Uusitupa, Jaana Lindström, Anne M. Louheranta, Johan Gunnar Eriksson, Timo T. Valle, Helena Hämäläinen, Pirjo Ilanne‐Parikka, Sirkka M Keinanen-Kiukaanniemi, Markku Laakso et al. · 2002 · Diabetes
103. Decreased food intake and body weight in pancreatic polypeptide-overexpressing mice
     Naohiko Ueno, Akio Inui, Masako Iwamoto, Toshihiro Kaga, Akihiro Asakawa, Minoru Okita, Mineko Fujimiya, Yoshito Nakajima, Yasukazu Ohmoto, Masaharu OHNAKA et al. · 1999 · Gastroenterology
104. Adiponectin Gene Polymorphisms and Adiponectin Levels Are Independently Associated With the Development of Hyperglycemia During a 3-Year Period
     Frédéric Fumeron, Roberte Aubert, Afshan Siddiq, Dina Betoulle, Frank Péan, Samy Hadjadj, Jean Tichet, Elsie Wilpart, Marie‐Claude Chesnier, Beverley Balkau et al. · 2004 · Diabetes
105. Identification of quantitative trait loci affecting carcass composition in swine: I. Fat deposition traits.
     Gary Alan Rohrer, John W. Keele · 1998 · Journal of Animal Science
106. Homozygosity of the Pro12Ala variant of the peroxisome proliferation-activated receptor-γ2 (PPAR-γ2): divergent modulating effects on body mass index in obese and lean Caucasian men
     Jakob Ek, Søren A. Urhammer, Thorkild I. A. Sørensen, T Andersen, Johan H. Auwerx, Oluf Borbye Pedersen · 1999 · Diabetologia
107. A Gene for Congenital Generalized Lipodystrophy Maps to Human Chromosome 9q34
     Abhimanyu Garg, Ross Wilson, Robert Barnes, Elif Arioǧlu, Zohra Zaidi, Figen Gürakan, Nurten Koçak, Stephen O’Rahilly, Simeon I. Taylor, Shailendra B. Patel et al. · 1999 · The Journal of Clinical Endocrinology & Metabolism
108. Identification and functional analysis of novel human melanocortin-4 receptor variants.
     Wei Gu, Zhiguang Tu, Patrick W. Kleyn, Ahmed H. Kissebah, Laura J. Duprat, J. Lee, W Chin, Sanchit Maruti, N Deng, Stewart L. Fisher et al. · 1999 · Diabetes
109. The PPAR‐gamma P12A polymorphism modulates the relationship between dietary fat intake and components of the metabolic syndrome: results from the Québec Family Study
     Julie Robitaille, Jean‐Pierre Després, Louis Përusse, Marie‐Claude Vohl · 2003 · Clinical Genetics
110. Abdominal Visceral Fat is Associated with a BclI Restriction Fragment Length Polymorphism at the Glucocorticoid Receptor Gene Locus
     B Buemann, Marie‐Claude Vohl, Monique Chagnon, Yvon C. Chagnon, Jacques Gagnon, Louis Përusse, France T. Dionne, Jean‐Pierre Després, Angelo Tremblay, André Nadeau et al. · 1997 · Obesity Research
111. Lysosomal acid lipase-deficient mice: depletion of white and brown fat, severe hepatosplenomegaly, and shortened life span
     Hong Du, Martin Heur, Ming Duanmu, Gregory Alex Grabowski, David Y. Hui, David P. Witte, Jaya Mishra · 2001 · Journal of Lipid Research
112. A single nucleotide polymorphism (SNP) in the leptin receptor is associated with BMI, fat mass and leptin levels in postmenopausal Caucasian women
     Naomi D. Quinton, Allison Lee, Richard John M Ross, Richard Eastell, Alexandra I. F. Blakemore · 2001 · Human Genetics
113. Functional Characterization of Melanocortin-4 Receptor Mutations Associated with Childhood Obesity
     Ya‐Xiong Tao, Deborah L. Segaloff · 2003 · Endocrinology
114. Transgenic expression of myostatin propeptide prevents diet-induced obesity and insulin resistance
     Zhao, Baoping, Wall, Robert J., Yang, Jinzeng · 2005 · Biochemical and Biophysical Research Communications
115. Lithium: a review of its metabolic adverse effects
     Callum Livingstone, Hagen Rampes · 2006 · Journal of Psychopharmacology
116. Mkks-null mice have a phenotype resembling Bardet–Biedl syndrome
     Melissa A. Fath, Robert F. Mullins, Charles C. Searby, Darryl Y. Nishimura, Jun Wei, Kamal Rahmouni, Roger E. Davis, Marwan K. Tayeh, Michael Andrews, Baoli Yang et al. · 2005 · Human Molecular Genetics
117. DNA polymorphism in the uncoupling protein (UCP) gene and human body fat.
     JM Oppert, Marie‐Claude Vohl, M Chagnon, France T. Dionne, Anne‐Marie Cassard, Daniel Ricquier, Louis Përusse, Claude Bouchard · 1994 · PubMed
118. The Human Magel2 Gene and Its Mouse Homologue Are Paternally Expressed and Mapped to the Prader-Willi Region
     Irène Boccaccio, Heather R. Glatt-Deeley, Françoise Watrin A, Nathalie Roëckel, Marc Lalande, Françoise Muscatelli · 1999 · Human Molecular Genetics
119. Stromelysin-3 Is a Potent Negative Regulator of Adipogenesis Participating to Cancer Cell-Adipocyte Interaction/Crosstalk at the Tumor Invasive Front
     Kumari L. Andarawewa, Elena Roza Motrescu, Marie‐Pierre Chenard, Anne Gansmüller, Isabelle Stoll, Catherine Tomasetto, Marie‐Christine Rio · 2005 · Cancer Research
120. Mapping quantitative trait loci for murine growth: a closer look at genetic architecture
     Ty T. Vaughn, L. Susan Pletscher, Andréa Cristina Peripato, Kelly King‐Ellison, EMILY ADAMS, Christopher F. Erikson, James M. Cheverud · 1999 · Genetics Research
121. Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15
     Rivka Carmi, Tatiana Rokhlina, Anne E. Kwitek, Khalil Elbedour, Darryl Y. Nishimura, Edwin M. Stone, Val C. Sheffield · 1995 · Human Molecular Genetics
122. Identification of four chromosomal loci determining obesity in a multifactorial mouse model.
     Craig H. Warden, Janis S. Fisler, Scott Shoemaker · 1995 · Journal of Clinical Investigation
123. Alms1-disrupted mice recapitulate human Alström syndrome
     Gayle B. Collin, Erika M. Cyr, Roderick Terry Bronson, Jan D. Marshall, Elaine J Gifford, Wanda L. Hicks, Stephen A. Murray, Quzhao Zheng, Richard S. Smith, Patsy M. Nishina et al. · 2005 · Human Molecular Genetics
124. Indication for Linkage of the Human OB Gene Region With Extreme Obesity
     Karine Clément, Chad P. Garner, Jörg Hager, Anne Philippi, Carrie LeDuc, Alisoun H. Carey, Timothy JR Harris, Corinne Jury, Lon R. Cardon, Arnaud Basdevant et al. · 1996 · Diabetes
125. Familial Dwarfism due to a Novel Mutation of the Growth Hormone-Releasing Hormone Receptor Gene
     Roberto Salvatori · 1999 · The Journal of Clinical Endocrinology & Metabolism
126. Autosomal Genomic Scan for Loci Linked to Obesity and Energy Metabolism in Pima Indians
     R.A. Norman, Pietro Antonio Tataranni, Richard E. Pratley, D. Bruce Thompson, Robert L. Hanson, Michal Procházka, Leslie J. Baier, Margaret G. Ehm, H. Sakul, Tatiana Foroud et al. · 1998 · The American Journal of Human Genetics
127. Linkage of Bardet–Biedl syndrome to chromosome 16q and evidence for non–allelic genetic heterogeneity
     Anne E. Kwitek, Rivka Carmi, Geoffrey M. Duyk · 1993 · Nature Genetics
128. Generation of Viable Cholesterol-Free Mice
     Andrew S. Wechsler, Anat Brafman, Millicent Shafir, Maura Heverin, Howard Gottlieb, Golda M. Damari, S. Gozlan-Kelner, Igor Spivak, Olga Moshkin, Eddie Fridman et al. · 2003 · Science
129. Alternative Gnas gene products have opposite effects on glucose and lipid metabolism
     Min Chen, Oksana Gavrilova, Jie Liu, Tao Xie, Chu‐Xia Deng, Annie Nguyen, Lisa M. Nackers, Javier Lorenzo, Laura Shen, Lee Scott Weinstein · 2005 · Proceedings of the National Academy of Sciences
130. The Human Obesity Gene Map: The 2001 Update
     Tuomo Rankinen, Louis Përusse, S. John Weisnagel, Eric E. Snyder, Yvon C. Chagnon, Claude Bouchard · 2002 · Obesity Research
131. Absence of Cocaine- and Amphetamine-Regulated Transcript Results in Obesity in Mice Fed a High Caloric Diet
     Mark Asnicar, Dennis P. Smith, Derek D. Yang, Mark L. Heiman, Niles Wayne Fox, Yun-Fei Chen, Hansen M. Hsiung, Anja M. Koster · 2001 · Endocrinology
132. The Spectrum of Mutations in TBX3: Genotype/Phenotype Relationship in Ulnar-Mammary Syndrome
     Bamshad, M., Le, T., Watkins, W.S., Dixon, M.E., Kramer, B.E., Roeder, A.D., Carey, J.C., Root, S., Schinzel, A., Van Maldergem, L. et al. · 1999 · The American Journal of Human Genetics
133. Idiopathic Weight Reduction in Mice Deficient in the High-Mobility-Group Transcription Factor Sox8
     Elisabeth Sock, Katy Schmidt, Irm Hermanns-Borgmeyer, Michael R. Bösl, Michael Wegner · 2001 · Molecular and Cellular Biology
134. The CAG repeat polymorphism in the androgen receptor gene modulates body fat mass and serum concentrations of leptin and insulin in men
     Michael Zitzmann, Jörg Gromoll, Arnold von Eckardstein, Eberhard Nieschlag · 2003 · Diabetologia
135. Genetic variation in the human vitamin D receptor is associated with muscle strength, fat mass and body weight in Swedish women
     Elin Grundberg, Helena Brändström, Eva L. Ribom, Östen Ljunggren, Hans Mallmin, Andreas Kindmark · 2004 · European Journal of Endocrinology
136. Glucose-dependent insulinotropic polypeptide receptor knockout mice have altered bone turnover
     Ding Xie, Hua Cheng, Mark W. Hamrick, Qing Zhong, Ke-Hong Ding, Daniel José Correa, Sandra Williams, Anthony L. Mulloy, Wendy Bollinger Bollag, Roni J. Bollag et al. · 2005 · Bone
137. Association of polymorphisms in the ?2-adrenergic receptor gene with obesity, hypertriglyceridaemia, and diabetes mellitus (Short Communication)
     Satomi Ishiyama-Shigemoto, Kentaro Yamada, Xiaohong Yuan, Fumi Ichikawa, K. Nonaka · 1999 · Diabetologia
138. Impact of the Peroxisome Proliferator Activated Receptor γ2 Pro12Ala polymorphism on adiposity, lipids and non-insulin-dependent diabetes mellitus
     Aline Meirhaeghe, Lluis Fajas A, Nicole Helbecque, Dominique Cottel, Johan H. Auwerx, SS Deeb, Philippe Amouyel · 2000 · International Journal of Obesity
139. ENPP1/PC-1 K121Q Polymorphism and Genetic Susceptibility to Type 2 Diabetes
     Nicola I. Abate, Manisha Chandalia, Pankaj Satija, BEVERLEY A. ADAMS-HUET, Scott M. Grundy, Sandeep Sreedharan, Venkatesan Radha, R Deepa, Viswanathan Mohan · 2005 · Diabetes
140. Maternal Environment and Genotype Interact to Establish Diabesity in Mice
     Peter C. Reifsnyder, Gary A. Churchill, Edward H. Leiter · 2000 · Genome Research
141. Regulation of Glucose Transporter SGLT1 by Ubiquitin Ligase Nedd4‐2 and Kinases SGK1, SGK3, and PKB
     Michael Dieter, Mònica Palmada, Jeyaganesh Rajamanickam, Atakan Aydın, Andreas Busjahn, Christoph Boehmer, Friedrich Cameron Luft, Florian J.W. Lang · 2004 · Obesity Research
142. Novel polymorphisms in the 5' region of the LEP gene: association with leptin levels and response to low-calorie diet in human obesity.
     Olivier Mammes, Dina Betoulle, Roberte Aubert, V Giraud, S Tuzet, Anne Petiet, N. Colas-Linhart, Frédéric Fumeron · 1998 · Diabetes
143. Mest/Peg1 imprinted gene enlarges adipocytes and is a marker of adipocyte size
     Mayumi M. Takahashi, Yasutomi Kamei, Osamu Ezaki · 2004 · American Journal of Physiology-Endocrinology and Metabolism
144. Vitamin D receptor gene polymorphisms are associated with obesity in type 2 diabetic subjects with early age of onset
     WZ Ye, AF Reis, Danièle Dubois‐Laforgue, Christine Bellanné‐Chantelot, José Timsit, Gilberto Velho · 2001 · European Journal of Endocrinology
145. Genetic Variation in the Renin–Angiotensin System and Abdominal Adiposity in Men: The Olivetti Prospective Heart Study
     Pasquale Strazzullo, Roberto Iacone, Licia Iacoviello, Ornella Russo, Gianvincenzo Barba, Paola Russo, Andria D’Orazio, Antonio Barbato, Francesco Paolo Cappuccio, Eduardo Farinaro et al. · 2003 · Annals of Internal Medicine
146. Effect of liver fatty acid binding protein (FABP) T94A missense mutation on plasma lipoprotein responsiveness to treatment with fenofibrate
     Charles Brouillette, Yohan Bossé, Louis Përusse, Daniel Gaudet, Marie‐Claude Vohl · 2004 · Journal of Human Genetics
147. Whole Genome Scan for Obstructive Sleep Apnea and Obesity in African-American Families
     Lyle John Palmer, Sarah G. Buxbaum, Emma K. Larkin, Sanjay R. Patel, Robert C. Elston, Peter V. Tishler, Susan S Redline · 2004 · American Journal of Respiratory and Critical Care Medicine
148. Severely altered guanidino compound levels, disturbed body weight homeostasis and impaired fertility in a mouse model of guanidinoacetate N-methyltransferase (GAMT) deficiency
     A. Schmidt · 2004 · Human Molecular Genetics
149. 5′ Flanking Variants of Resistin Are Associated With Obesity
     James C. Engert, Marie‐Claude Vohl, Scott M. Williams, Pierre Lepage, Jorge Loredo‐Osti, Janet Faith, Carole Doré, Yannick Renaud, Noël P. Burtt, Amélie Villeneuve et al. · 2002 · Diabetes
150. Quantitative trait loci affecting fatness in the chicken
     C. O. N. Ikeobi, John Arthur Woolliams, David Morrice, Andy S Law, Dawn Windsor, David W. Burt, P.M. Hocking · 2002 · Animal Genetics
151. Mutations of thePRKAR1AGene in Cushing’s Syndrome due to Sporadic Primary Pigmented Nodular Adrenocortical Disease
     Lionel Groussin, Eric H. Jullian, Karine Perlemoine, Albert Louvel, Bruno Leheup, JEAN PIERRE LUTON, XAVIER Y. BERTAGNA, Jerome Yves Bertherat · 2002 · The Journal of Clinical Endocrinology & Metabolism
152. LXRβ Is Required for Adipocyte Growth, Glucose Homeostasis, and β Cell Function
     Isabelle Gerin, Vernon Wayne Dolinsky, Jonathan G. Shackman, Robert T. Kennedy, Shian-Huey Chiang, Charles Burant, Knut Rune Steffensen, Jan-Ακε Gustafsson, Ormond A. MacDougald · 2005 · Journal of Biological Chemistry
153. Obesity and hyperleptinemia in metallothionein (-I and -II) null mice
     John H. Beattie, A. M. Wood, April M. Newman, Ian Bremner, K.H. Andy Choo, Anna Michalska, J. S. Duncan, Paul Trayhurn · 1998 · Proceedings of the National Academy of Sciences
154. Attenuation of Diet-Induced Weight Gain and Adiposity through Increased Energy Expenditure in Mice Lacking Angiotensin II Type 1a Receptor
     Ryuji Kouyama, Takayoshi Suganami, Junko Nishida, Miyako Tanaka, Takuya Toyoda, Minako Kiso, Tsuyoshi Chiwata, Yoshihiro Miyamoto, Yasunao Yoshimasa, Akiyoshi Fukamizu et al. · 2005 · Endocrinology
155. Autosomal-Dominant Mode of Inheritance of a Melanocortin-4 Receptor Mutation in a Patient with Severe Early-Onset Obesity Is Due to a Dominant-Negative Effect Caused by Receptor Dimerization
     Heike Biebermann, Heiko Krude, Andrea Elsner, Vladimir Chubanov, Thomas W. Gudermann, Annette Grüters · 2003 · Diabetes
156. Targeted Disruption of the Pituitary Adenylate Cyclase-Activating Polypeptide Gene Results in Early Postnatal Death Associated with Dysfunction of Lipid and Carbohydrate Metabolism
     Sarah Louise Gray, Kevin James Cummings, Frank Robert Jirik · 2001 · Molecular Endocrinology
157. Association of the Polycystic Ovary Syndrome with Genomic Variants Related to Insulin Resistance, Type 2 Diabetes Mellitus, and Obesity
     José L. San Millán, Marta Cortón, Gemma Villuendas, José Sancho, Belén Peral, Héctor Francisco Escobar-Morreale · 2004 · The Journal of Clinical Endocrinology & Metabolism
158. A Thyroid Hormone Receptor α Gene Mutation (P398H) Is Associated with Visceral Adiposity and Impaired Catecholamine-stimulated Lipolysis in Mice
     Yan‐Yun Liu, James J. Schultz, Gregory A. Brent · 2003 · Journal of Biological Chemistry
159. Mutations in the small heterodimer partner gene are associated with mild obesity in Japanese subjects
     Hidekazu Nishigori, Hideaki Tomura, Naoko Tonooka, Masao Kanamori, Shirou Yamada, Kimie Sho, Ituro Inoue, Nobuyuki Kikuchi, Kazumichi Onigata, Itaru Kojima et al. · 2001 · Proceedings of the National Academy of Sciences
160. The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci.
     R. Watanabe, Soumitra S. Ghosh, Carl D. Langefeld, T. Valle, Elizabeth R. Hauser, Victoria L. Magnuson, K. Mohlke, K. Silander, D. S. Ally, P. Chines et al. · 2000 · American Journal of Human Genetics
161. The ER22/23EK polymorphism in the glucocorticoid receptor gene is associated with a beneficial body composition and muscle strength in young adults
     van Rossum, Elisabeth F. C., Voorhoeve, Paul G., te Velde, Saskia J., Koper, Jan W., Delemarre-van de Waal, Henriette A., Kemper, Han C. G., Lamberts, Steven W. J. · 2004 · The Journal of Clinical Endocrinology & Metabolism
162. The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome
     René Santer, Sebastian Groth, Martina Kinner, Anja Dombrowski, Gerard T. Berry, Johannes Brodehl, James V. Leonard, SHIMON W. MOSES, Svante Norgren, Flemming Skovby et al. · 2001 · Human Genetics
163. Hypogonadism and obesity in mice with a targeted deletion of the Nhlh2 gene
     Deborah J. Good, Forbes D. Porter, Kathleen A. Mahon, Albert F. Parlow, Heiner Westphal, Ilan Richard Kirsch · 1997 · Nature Genetics
164. A Genome-Wide Scan for Childhood Obesity–Associated Traits in French Families Shows Significant Linkage on Chromosome 6q22.31-q23.2
     David Meyre, Cécile Lecœur, Jérôme Delplanque, Stephan Francke, Vincent Vatin, Emmanuelle Durand, Jacques Weill, Christian Dina C, Philippe Froguel · 2004 · Diabetes
165. A genetic variation in the 5 ′ flanking region of the UCP3 gene is associated with body mass index in humans in interaction with physical activity
     Shuichi Otabe, Karine Clément, Christian Dina C, Véronique Pelloux, Bernard Guy-grand, Philippe Froguel, Francis Vasseur · 2000 · Diabetologia
166. Resistance to high-fat diet-induced obesity and altered expression of adipose-specific genes in HSL-deficient mice
     Kenji Harada, Wen‐Jun Shen, Shailja Patel, Vanita S. Natu, Jining Wang, Jun-ichi Osuga, Shun Ishibashi, Fredric B. Kraemer · 2003 · American Journal of Physiology-Endocrinology and Metabolism
167. Association analysis of genes involved in the leptin-signaling pathway with obesity in Brazil
     Vanessa S. Mattevi, Verônica Marques Zembrzuski, Mara Helena Hutz · 2002 · International Journal of Obesity
168. Evidence for an important role of perilipin in the regulation of human adipocyte lipolysis
     Ingalena Andersson, Peter Arner, Salim Mottagui‐Tabar, M. Ryd�n, P. L�fgren, Gary Faulds, J. Hoffstedt, Anthony J. Brookes · 2003 · Diabetologia
169. Induced Adiposity and Adipocyte Hypertrophy in Mice Lacking the AMP-Activated Protein Kinase-α2 Subunit
     Josep A. Villena, Benoı̂t Viollet, Fabrizzio Andreelli, Axel Kahn, Sophie Vaulont, Hei Sook Sul · 2004 · Diabetes
170. Lipid and carbohydrate metabolism in mice with a targeted mutation in the IL-6 gene: absence of development of age-related obesity
     Gina B. Di Gregorio, Lori L. Hensley, Tong Lü, Gouri Ranganathan, Philip A. Kern · 2004 · American Journal of Physiology-Endocrinology and Metabolism
171. Linkage and Association Studies between the Melanocortin Receptors 4 and 5 Genes and Obesity-Related Phenotypes in the Québec Family Study
     Yvon C. Chagnon, Wenji Chen, Louis Përusse, Monique Chagnon, André Nadeau, William O. Wilkison, Claude Bouchard · 1997 · Molecular Medicine
172. Longitudinal Hormonal and Pituitary Imaging Changes in Two Females with Combined Pituitary Hormone Deficiency due to Deletion of A301,G302 in the PROP1 Gene1
     Berenice Bilharinho Mendonca, Maria G. F. Osorio, Ana Claudia Latronico · 1999 · The Journal of Clinical Endocrinology & Metabolism
173. Associations between the Leptin Receptor Gene and Adiposity in Middle-Aged Caucasian Males from the HERITAGE Family Study
     Yvon C. Chagnon, Jack H. Wilmore, Ingrid B. Borecki, Jacques Gagnon, Louis Përusse, Monique Chagnon, Gregory Collier, Arthur S. Leon, James S. Skinner, D. C. Rao et al. · 2000 · The Journal of Clinical Endocrinology & Metabolism
174. A Polymorphic CYP19 TTTA Repeat Influences Aromatase Activity and Estrogen Levels in Elderly Men: Effects on Bone Metabolism
     Luigi Gennari, Laura Masi, Daniela Merlotti, Lucia Picariello, Alberto Falchetti, Annalisa Tanini, Carmelo Mavilia, Francesca Del Monte, Stefano Gonnelli, Barbara Lucani et al. · 2004 · The Journal of Clinical Endocrinology & Metabolism
175. Mapping of quantitative trait loci affecting quality and production traits in egg layers
     Maria Tuiskula-Haavisto, Mervi Honkatukia, Johanna Vilkki · 2002 · Poultry Science
176. Wnt10b Deficiency Promotes Coexpression of Myogenic and Adipogenic Programs in Myoblasts
     Vertino, Anthony M., Taylor-Jones, Jane M., Longo, Kenneth A., Bearden, Edward D., Lane, Timothy F., McGehee, Robert E., MacDougald, Ormond A., Peterson, Charlotte A. · 2005 · Molecular Biology of the Cell
177. Localization of the gene for familial partial lipodystrophy (Dunnigan variety) to chromosome 1q21–22
     John M. Peters, Robert Barnes, Lynda B. Bennett, William M. Gitomer, Anne M. Bowcock, Abhimanyu Garg · 1998 · Nature Genetics
178. Genetic Analysis of a New Mouse Model for Non-Insulin-Dependent Diabetes
     Jung Han Kim, Śaunak Sen, Cindy Avery, Elizabeth Simpson, Phillip Chandler, Patsy M. Nishina, Gary A. Churchill, Jürgen Κ. Naggert · 2001 · Genomics
179. Clozapine‐induced weight gain associated with the 5HT2C receptor −759C/T polymorphism
     Del D. Miller, Vicki L. Ellingrod, Timothy L. Holman · 2005 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
180. A Genomewide Linkage Scan for Quantitative-Trait Loci for Obesity Phenotypes
     Hong‐Wen Deng, Hongyi Deng, Yong-Jun Liu, Yao-Zhong Liu, Fu-Hua Xu, Hui Shen, Theresa Conway, Jinlong Li, Qing-Yang Huang, K. Michael Davies et al. · 2002 · The American Journal of Human Genetics
181. Expression and imprinting of MAGEL2 suggest a role in Prader-Willi syndrome and the homologous murine imprinting phenotype
     Siu Fai Lee · 2000 · Human Molecular Genetics
182. Polymorphisms in the ABCG5 and ABCG8 genes associate with cholesterol absorption and insulin sensitivity
     Helena K. Gylling, Maarit Hallikainen, Jussi Pihlajamäki · 2004 · Journal of Lipid Research
183. A Variation in the Ghrelin Gene Increases Weight and Decreases Insulin Secretion in Tall, Obese Children
     Márta Korbonits, Maria Gueorguiev, Eithne O’Grady, Cécile Lecœur, Daniel Swan, Charles A. Mein, Jacques Weill, Ashley Barry Grossman, Philippe Froguel · 2002 · The Journal of Clinical Endocrinology & Metabolism
184. β2-adrenoceptor gene polymorphism, body weight, and physical activity
     Aline Meirhaeghe, Nicole Helbecque, Dominique Cottel, Philippe Amouyel · 1999 · The Lancet
185. Targeted disruption of H3 receptors results in changes in brain histamine tone leading to an obese phenotype
     Kazuhiko Takahashi, Hiroaki Suwa, Tomo-o Ishikawa, Hidehito Kotani · 2002 · Journal of Clinical Investigation
186. Association of polymorphisms in the estrogen receptor α gene with body fat distribution
     T Okura, Michiko Koda, Fujiko Ando, Naoakira Niino, Shigeo Ohta, Hiroshi Shimokata · 2003 · International Journal of Obesity
187. Single Nucleotide Polymorphisms in the Proximal Promoter Region of the Adiponectin (APM1) Gene Are Associated With Type 2 Diabetes in Swedish Caucasians
     Harvest F. Gu, Adili Abulaiti, Claes‐Göran Östenson, Keith Humphreys, Claes Wahlestedt, Anthony J. Brookes, Suad Efendić · 2004 · Diabetes
188. Construction and Analysis of Mouse Strains Lacking the Ubiquitin Ligase UBR1 (E3α) of the N-End Rule Pathway
     Yong Tae Kwon, Zanxian Xia, Ilia V. Davydov, Stewart H. Lecker, Alexander J. Varshavsky · 2001 · Molecular and Cellular Biology
189. Dietary obesity linked to genetic loci on chromosomes 9 and 15 in a polygenic mouse model.
     David B. West, J. Goudey-Lefevre, Barbara York, Gary E. Truett · 1994 · Journal of Clinical Investigation
190. Phenotypes in Three Pedigrees with Autosomal Dominant Obesity Caused by Haploinsufficiency Mutations in the Melanocortin-4 Receptor Gene
     Mani Sina, Anke Hinney, Andreas Ziegler, Tanja Neupert, Hermann Georg Mayer, Wolfgang Siegfried, Werner Friedrich Blum, Helmut Remschmidt, Johannes Hebebrand · 1999 · The American Journal of Human Genetics
191. Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophy.
     Louise C. Wilson, M E Oude Luttikhuis, Peter Theodore Clayton · 1994 · Journal of Medical Genetics
192. A Genome-Wide Scan for Abdominal Fat Assessed by Computed Tomography in the Quebec Family Study
     Louis Përusse, Treva Rice, Yvon C. Chagnon, Jean‐Pierre Després, Simone Lemieux, Sonia Roy, Michel Lacaille, My-Ann Ho-Kim, Monique Chagnon, Michael A. Province et al. · 2001 · Diabetes
193. In Vivo Analysis of Growth Hormone Receptor Signaling Domains and Their Associated Transcripts
     Jennifer Rowland, Agnieszka M Lichanska, Linda M. Kerr, Mary E. White, Elisabetta d’Aniello, Sheryl Maher, Richard J. P. Brown, Rohan David Teasdale, Peter G. Noakes, Michael J. Waters · 2004 · Molecular and Cellular Biology
194. Vitamin D Receptor Genotype Is Associated With Fat-Free Mass and Sarcopenia in Elderly Men
     Stephen M. Roth, Joseph M. Zmuda, Jane A. Cauley, P. R. Shea, R. E. Ferrell · 2004 · The Journals of Gerontology Series A
195. Increased sensitivity to K+ deprivation in colonic H,K-ATPase-deficient mice.
     Pierre Meneton, Patrick J. Schultheis, J Greeb · 1998 · Journal of Clinical Investigation
196. Paternal versus maternal transmission of a stimulatory G-protein α subunit knockout produces opposite effects on energy metabolism
     Shuhua Yu, Oksana Gavrilova, Hui Chen, Randy Lee, Jie Liu, Karel Pacák, A F Parlow, Michael J. Quon, Marc L. Reitman, Lee Scott Weinstein · 2000 · Journal of Clinical Investigation
197. Adrenal involvement in multiple endocrine neoplasia type 1
     Langer, Peter, Cupisti, Kenko, Bartsch, Detlef K., Nies, Christoph, Goretzki, Peter E., Rothmund, Matthias, Röher, Hans D. · 2002 · World Journal of Surgery
198. Phosphatidylcholine Homeostasis and Liver Failure
     Zhaoyu Li, Luis B. Agellon, Dennis E. Vance · 2005 · Journal of Biological Chemistry
199. Extreme Obesity May Be Linked to Markers Flanking the Human OB Gene
     Danielle R. Reed, Yuan Chun Ding, Weizhen Xu · 1996 · Diabetes
200. A Combined Analysis of Genomewide Linkage Scans for Body Mass Index, from the National Heart, Lung, and Blood Institute Family Blood Pressure Program
     Xiaodong Wu, Richard S. Cooper, Ingrid B. Borecki · 2002 · The American Journal of Human Genetics