Analysis of Human Genetic Linkage

Ott, Jurg·1999·Johns Hopkins University Press eBooks
DOI 10.56021/9780801861406

Cited by (755)

Items 101–200 of 755

  1. A Third-Pass Genome Scan in Panic Disorder: Evidence for Multiple Susceptibility Loci
    Abby J. Fyer, Steven P. Hamilton, Martina Durner, Fatemeh G. Haghighi, Gary A. Heiman, Ramiro Costa, Oleg Vadimovich Evgrafov, Philip Adams, Ada Baisre de Leon, Nilda Taveras et al. · 2006 · Biological Psychiatry
  2. Association of NOD2 with Crohn's Disease in a homogenous Irish population
    Emer Bairead, Dawn L. Harmon, Annie M. Curtis, Yvette Kelly, Clare O’Leary, Michelle J. Gardner, Dermot T. Leahy, Pat Vaughan, Denise Keegan, Colm A O'Morain et al. · 2003 · European Journal of Human Genetics
  3. Genome Association Studies of Complex Diseases by Case-Control Designs
    Ruzong Fan, Michael Knapp · 2003 · The American Journal of Human Genetics
  4. Common Variants in Glutamine:Fructose-6-Phosphate Amidotransferase 2 (GFPT2) Gene Are Associated with Type 2 Diabetes, Diabetic Nephropathy, and Increased GFPT2 mRNA Levels
    Hailing Zhang, Yiwen Jia, Judith J. Cooper, Terri C. Hale, Zhengxian Zhang, Steven C. Elbein · 2004 · The Journal of Clinical Endocrinology & Metabolism
  5. The likelihood ratio test for homogeneity in finite mixture models
    Hanfeng Chen, Jiahua Chen · 2001 · Canadian Journal of Statistics
  6. Association between vitamin D receptor gene polymorphisms and tubular citrate handling in calcium nephrolithiasis
    Giuseppe Mossetti, Pietro Vuotto, Domenico Rendina · 2003 · Journal of Internal Medicine
  7. Association analysis of polymorphisms in the upstream region of the human dopamine D4 receptor gene (DRD4) with schizophrenia and personality traits
    H. Mitsuyasu, Naotsugu Hirata, Yasunari Sakai, Hiroki Shibata, Yasuhiko Takeda, Hideaki Ninomiya, Hiroaki Kawasaki, Naonori Tashiro, Y Fukumaki · 2001 · Journal of Human Genetics
  8. Identification of VAV2 on 9q34 and its exclusion as the tuberous sclerosis gene TSC1
    Elizabeth P. Henske, M. Priscilla Short, Sergiusz Jóźwiak, C. M. BOVEY, Sarvan K. Ramlakhan, Jonathan L. Haines, David J. Kwiatkowski · 1995 · Annals of Human Genetics
  9. Variations in HSP70 genes associated with noise-induced hearing loss in two independent populations
    Annelies Konings, Lut Van Laer, Sophie Michel et al. · 2008 · European Journal of Human Genetics
  10. Jannovar: A Java Library for Exome Annotation
    Marten Jäger, Kai Wang, Sebastian Bauer, Damian P. Smedley, Peter Michael Krawitz, Peter N. Robinson · 2014 · Human Mutation
  11. Evaluating the Results of Genomewide Linkage Scans of Complex Traits by Locus Counting
    Steven Wiltshire, Lon R. Cardon, Mark I. McCarthy · 2002 · The American Journal of Human Genetics
  12. Multiple susceptibility loci for multiple sclerosis
    The Multiple Sclerosis Genetics Group · 2002 · Human Molecular Genetics
  13. Combining extremely concordant sibpairs with extremely discordant sibpairs provides a cost effective way to linkage analysis of quantitative trait loci
    C. Charles Gu, A.A. Todorov, D. C. Rao · 1996 · Genetic Epidemiology
  14. The First Comprehensive Genetic Linkage Map of a Marsupial: The Tammar Wallaby (Macropus eugenii)
    Kyall Richard Zenger, Louise M. McKenzie, Desmond W. Cooper · 2002 · Genetics
  15. A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency
    Raskind, W H, Igo, R P, Chapman, N H, Berninger, V W, Thomson, J B, Matsushita, M, Brkanac, Z, Holzman, T, Brown, M, Wijsman, E M · 2005 · Molecular Psychiatry
  16. Branchio–oto–renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analyses
    K. M. Sanggaard, Nanna Dahl Rendtorff, Klaus Wilbrandt Kjaer · 2007 · European Journal of Human Genetics
  17. Effects of Stratification in the Analysis of Affected-Sib-Pair Data: Benefits and Costs
    Suzanne M. Leal, Jürg Ott · 2000 · The American Journal of Human Genetics
  18. Genome‐wide scan of Swedish families with hereditary prostate cancer: Suggestive evidence of linkage at 5q11.2 and 19p13.3
    Fredrik E. Wiklund, Elizabeth M. Gillanders, Julie A. Albertus et al. · 2003 · The Prostate
  19. The variant Arg110Gln of human IL-13 is associated with an immunologically hyper-reactive form of onchocerciasis (sowda)
    Achim M. Hoerauf, Susanne Kruse, Norbert W. Brattig, Andrea Heinzmann, B. Mueller-Myhsok, Klaus A. Deichmann · 2002 · Microbes and Infection
  20. Interleukin‐10 promoter polymorphisms and atopic asthma in North Indians
    Rajshekhar Chatterjee, Jyotsna Batra, Amrendra Kumar · 2005 · Clinical & Experimental Allergy
  21. Using linked markers to infer the age of a mutation
    Bruce H. Rannala, Giorgio Bertorelle · 2001 · Human Mutation
  22. Mapping a novel locus for familial atrial fibrillation on chromosome 10p11-q21
    Paul G.A. Volders, Qian Zhu, Carl C. Timmermans, Petra M.H. Eurlings, Xiaoyan Su, Yvonne H. J. M. Arens, Li Li, Roselie J. E. Jongbloed, Min Xia, Luz‐Maria Rodriguez et al. · 2006 · Heart Rhythm
  23. A linkage map of the porcine genome from a large‐scale White Duroc × Erhualian resource population and evaluation of factors affecting recombination rates
    Yuanmei Guo, Huirong Mao, Jun Ren et al. · 2009 · Animal Genetics
  24. A Susceptibility Locus on Chromosome 6q Greatly Increases Lung Cancer Risk among Light and Never Smokers
    Christopher Ian Amos, Susan M. Pinney, Yafang Li, Elena Y. Kupert, Juwon Lee, Mariza A. de Andrade, Ping Yang, Ann G. Schwartz, Pam R. Fain, Adi F. Gazdar et al. · 2010 · Cancer Research
  25. Association between vitamin D receptor gene polymorphisms and fasting idiopathic hypercalciuria in recurrent stone-forming patients
    Domenico Rendina, Giuseppe Mossetti, Roberto Viceconti · 2004 · Urology
  26. Submicroscopic subtelomeric 1qter deletions: a recognisable phenotype?
    Bert B A De Vries, SAMANTHA J L KNIGHT, TESSA HOMFRAY · 2001 · Journal of Medical Genetics
  27. GSNO reductase and β2-adrenergic receptor gene–gene interaction: bronchodilator responsiveness to albuterol
    Shweta Choudhry, Loretta G. Que, Zhonghui Yang, Limin Liu, Celeste S. Eng, Sung Ouk Kim, Gunjan Kumar, Shannon M. Thyne, Rocío Chapela, José Rodríguez‐Santana et al. · 2010 · Pharmacogenetics and Genomics
  28. On the Determination of Recombination Rates in Intermated Recombinant Inbred Populations
    Christopher R. Winkler, Nicole M Jensen, Mark Cooper · 2003 · Genetics
  29. A transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parents
    Derek Gordon, Chad A. Haynes, Christopher Johnnidis, Shailendra B. Patel, Anne M. Bowcock, Jürg Ott · 2004 · European Journal of Human Genetics
  30. Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13–15
    Krina T. Zondervan, Susan A. Treloar, Jianghai Lin, Daniel E. Weeks, Dale R. Nyholt, Jon Mangion, Ian Mackay, Lon R. Cardon, Nicholas G. Martin, Stephen Kennedy et al. · 2006 · Human Reproduction
  31. Maximum likelihood estimates of two-locus recombination fractions under some natural inequality restrictions
    Ying Zhou, Ningzhong Shi, Wing–Kam Fung · 2008 · BMC Genetics
  32. Analysis of linkage and linkage disequilibrium for eight X-STR markers
    Andreas O. Tillmar, Petter Mostad, Thore Egeland · 2008 · Forensic Science International Genetics
  33. Association of LOXL1 gene with Finnish exfoliation syndrome patients
    Susanna M. Lemmelä, Eva Forsman, Päivi Onkamo et al. · 2009 · Journal of Human Genetics
  34. Dopamine D4 receptor and tyrosine hydroxylase genes in bipolar disorder: evidence for a role of DRD4
    Pierandrea Muglia, Artūras Petronis, Emanuela Mundo, Sheila Lander, Tasha Cate‐Carter, James L. Kennedy · 2002 · Molecular Psychiatry
  35. Autosomal dominant thrombocytopenia: incomplete megakaryocyte differentiation and linkage to human chromosome 10
    Jonathan G. Drachman, Gail Pairitz Jarvik, Michele G. Mehaffey · 2000 · Blood
  36. Tumor Necrosis Factor Gene Complex in COPD and Disseminated Bronchiectasis
    Cristina Patuzzo, L. S. Gilè, Michele Zorzetto · 2000 · CHEST Journal
  37. Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis
    Lisa F. Barcellos, Ann B. Begovich, Rebecca Reynolds, Stacy J. Caillier, David Brassat, Silke Schmidt, Sarah E. Grams, Karen Walker, Lori L. Steiner, Bruce Cree et al. · 2004 · Annals of Neurology
  38. Novel genetic markers in the 5′‐flanking region of ANKH are associated with ankylosing spondylitis
    Florence W. L. Tsui, Hing Wo Tsui, Emily YiQin Cheng · 2003 · Arthritis & Rheumatism
  39. Association analysis of polymorphisms in serotonin 1B receptor (HTR1B) gene with heroin addiction: a comparison of molecular and statistically estimated haplotypes
    Dmitri Proudnikov, K. Steven LaForge, Heather Hofflich, Mark A. Levenstien, Derek Gordon, Sandra Barral, Jürg Ott, Mary Jeanne Kreek · 2006 · Pharmacogenetics and Genomics
  40. Applications of whole-genome high-density SNP genotyping
    David Wesley Craig, Dietrich A. Stephan · 2005 · Expert Review of Molecular Diagnostics
  41. Glutathione S-transferase M1, T1, and P1 polymorphisms and prostate cancer risk in middle-aged men
    Ilir Agalliu, Wendy J. Langeberg, Johanna W. Lampe · 2005 · The Prostate
  42. Pseudoxanthoma Elasticum Maps to an 820-kb Region of the p13.1 Region of Chromosome 16
    Olivier Le Saux, Zsolt Urbán, Harald H.H. Göring et al. · 1999 · Genomics
  43. Significant Evidence for Linkage Disequilibrium over a 5-cM Region among Afrikaners
    Derek Gordon, Ingrid Simonic, Jurg Ott · 2000 · Genomics
  44. Candidate genes showing no evidence for association or linkage with Alzheimer's disease using family-based methodologies
    Lars Bertram, Deborah Blacker, Adam Crystal, Kristina Mullin, Devon B. Keeney, Jennifer Lynn Jones, Sanjay Basu, Stephen Yhu, Suzanne Y. Guénette, Melvin G. McInnis et al. · 2000 · Experimental Gerontology
  45. Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q
    Sandra Pieke-Dahl, C G Möller, P M Kelley, L M Astuto, C W R J Cremers, M B Gorin, W J Kimberling · 2000 · Journal of Medical Genetics
  46. Strategies based on marker information for the study of human diseases
    Françoise Clerget‐Darpoux, Catherine Bonaïti‐Pellié · 1992 · Annals of Human Genetics
  47. EST and EST-SSR marker resources for Iris
    Shunxue Tang, Rebecca A Okashah, Marie‐Michèle Cordonnier‐Pratt, Lee H. Pratt, Virgil Ed Johnson, Christopher A Taylor, Michael L. Arnold, Steven J. Knapp · 2009 · BMC Plant Biology
  48. Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to Xp22.3
    Walter Lisch, Andreas Büttner, Frank Oeffner · 2000 · American Journal of Ophthalmology
  49. First-Generation Linkage Map of the Gray, Short-Tailed Opossum,Monodelphis domestica, Reveals Genome-Wide Reduction in Female Recombination Rates
    Paul B. Samollow, Candace M. Kammerer, Susan M. Mahaney, Jennifer L. Schneider, Scott J Westenberger, John L. VandeBerg, Edward S Robinson · 2004 · Genetics
  50. Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results
    Ruslan Dorfman, Weili Li, Lei Sun, Lin Fan, Yongqian Wang, Andrew J. Sandford, Peter D. Paré, Karen McKay, Hana Kayserova, Tereza Piskackova et al. · 2009 · Human Genetics
  51. Association of polymorphisms in IL-12/IFN-γ pathway genes with susceptibility to pulmonary tuberculosis in Indonesia
    Edhyana Sahiratmadja, Renée F. Baak-Pablo, Adriëtte W. de Visser · 2007 · Tuberculosis
  52. DNA marker-assisted selection of the polled condition in Charolais cattle
    S. M. Schmutz, F. L. S. Marquess, Tom G. Berryere · 1995 · Mammalian Genome
  53. Iron deficiency and NRAMP1 polymorphisms (INT4, D543N and 3′UTR) do not contribute to severity of anaemia in tuberculosis in the Indonesian population
    Edhyana Sahiratmadja, Frank Tammo Wieringa, Reinout van Crevel, Adriëtte W. de Visser, Iskandar Alisyahbana Adnan, Bachti Alisjahbana, P. Eline Slagboom, Sangkot Marzuki, Tom H. M. Ottenhoff, Esther van de Vosse et al. · 2007 · British Journal Of Nutrition
  54. American Founder Mutation for Attenuated Familial Adenomatous Polyposis
    Deborah Wood Neklason, Jeffery Stevens, Kenneth M. Boucher · 2007 · Clinical Gastroenterology and Hepatology
  55. Microsatellite instability is a genetic marker for the development of multiple gastric cancers
    Eiji Miyoshi, Ken Haruma, Toru Hiyama, Shinji Tanaka, Masaharu Yoshihara, Fumio Shimamoto, Kazuaki Chayama · 2001 · International Journal of Cancer
  56. Association of tryptophan hydroxylase gene polymorphism with depression, anxiety and comorbid depression and anxiety in a population‐based sample of postpartum Taiwanese women
    H. Sunny Sun, H‐W. Tsai, H‐C. Ko, F.M. Chang, T‐L. Yeh · 2004 · Genes Brain & Behavior
  57. Genetic Epidemiology of Infectious Diseases in Humans: Design of Population- Based Studies
    Laurent Abel, Alain J.J. Dessein · 1998 · Emerging infectious diseases
  58. A high-density SNP genetic linkage map for the silver-lipped pearl oyster, Pinctada maxima: a valuable resource for gene localisation and marker-assisted selection
    David B. Jones, Dean Robert Jerry, Mehar Singh Khatkar · 2013 · BMC Genomics
  59. A linkage analysis of sex determination in Bombus terrestris (L.) (Hymenoptera: Apidae)
    Jürgen Gadau, Christine U. Gerloff, Nadia Krüger · 2001 · Heredity
  60. A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees
    Mark Silberstein, Omer Weissbrod, Lars Otten, Anna Tzemach, Andrei Anisenia, Oren Shtark, Dvir Tuberg, Eddie Galfrin, Irena Gannon, Adel Shalata et al. · 2012 · Bioinformatics
  61. Family and case–control association study of the tumor necrosis factor-alpha (TNF-α) gene with schizophrenia and response to antipsychotic medication
    Gwyneth C. Zai, Daniel J. Müller, Jan Volavka, Pál Czobor, Jeffrey Alan Lieberman, Herbert Y. Meltzer, James L. Kennedy · 2006 · Psychopharmacology
  62. Combining Two-Stage Testing and Interval Mapping Strategies to Detect QTL for Resistance to Bonamiosis in the European Flat Oyster Ostrea edulis
    Delphine Lallias, Luis Gomez‐Raya, Chris Haley, Isabelle Arzul, Serge Heurtebise, A. R. Beaumont, Pierre Boudry, Sylvie Lapègue · 2009 · Marine Biotechnology
  63. Kinship testing with X-chromosomal markers: Mathematical and statistical issues
    Michael Krawczak · 2007 · Forensic Science International Genetics
  64. Genetic linkage mapping of turbot (Scophthalmus maximus L.) using microsatellite markers and its application in QTL analysis
    Xiaohong Ruan, Weiji Wang, Jie Kong, Fei Yu, Xueqin Huang · 2010 · Aquaculture
  65. Population genetic analysis of 12 X-STRs in Swedish population
    Andreas O. Tillmar · 2011 · Forensic Science International Genetics
  66. A comparative integrated gene-based linkage and locus ordering by linkage disequilibrium map for the Pacific white shrimp, Litopenaeus vannamei
    David B. Jones, Dean Robert Jerry, Mehar Singh Khatkar · 2017 · Scientific Reports
  67. Using X-chromosomal markers in relationship testing: Calculation of likelihood ratios taking both linkage and linkage disequilibrium into account
    Andreas O. Tillmar, Thore Egeland, Bertil Lindblom · 2010 · Forensic Science International Genetics
  68. Genomewide scan for real‐word reading subphenotypes of dyslexia: Novel chromosome 13 locus and genetic complexity
    R. Igo, N. H. Chapman, V. Berninger, M. Matsushita, Z. Brkanac, J. Rothstein, T. Holzman, K. Nielsen, W. H. Raskind, E. Wijsman · 2006 · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
  69. Dissecting genetic heterogeneity in autoimmune thyroid diseases by subset analysis
    Yaron Tomer, Francesca Menconi, Terry F. Davies, Giuseppe Barbesino, Roberto Rocchi, Aldo Pinchera, Erlinda Concepcion, David A. Greenberg · 2007 · Journal of Autoimmunity
  70. Linkage analysis of a large African family segregating stuttering suggests polygenic inheritance
    Muhammad Hashim Raza, Edward Michael Gertz, Jennifer Mundorff · 2012 · Human Genetics
  71. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14
    D Q, Michael L. Cuccaro, James M Jaworski, Carol S. Haynes, Dietrich A. Stephan, Jennifer M. Parod, Ruth K. Abramson, H H Wright, John R. Gilbert, Jonathan L. Haines et al. · 2006 · Molecular Psychiatry
  72. Linkage analysis of prostate cancer susceptibility: confirmation of linkage at 8p22–23
    Fredrik E. Wiklund, Björn‐Anders Jonsson, Ingela Göransson, Anders R. J. Bergh, Henrik Grönberg · 2003 · Human Genetics
  73. Effects of emergency remote instruction during the COVID-19 pandemic on university physics students in Italy
    Irene Marzoli, Arturo Colantonio, Claudio Fazio, Marco Giliberti, U. Scotti di Uccio, Italo Testa · 2021 · Physical Review Physics Education Research
  74. Linkage study of the alpha2A adrenergic receptor in attention-deficit hyperactivity disorder families.
    Chun Xu, R. Schachar, R. Tannock, W. Roberts, M. Malone, J. Kennedy, C. Barr · 2001 · American journal of medical genetics
  75. Prevalence and inheritance of hip osteoarthritis in Iceland
    Þorvaldur Ingvarsson · 2001 · Acta Orthopaedica Scandinavica
  76. The search for complex disease genes: fault by linkage or fault by association?
    Miron Baron · 2001 · Molecular Psychiatry
  77. Effect of linkage between vWA and D12S391 in kinship analysis
    Kristen Lewis O’Connor, Andreas O. Tillmar · 2012 · Forensic Science International Genetics
  78. Primordial Linkage of β2-Microglobulin to the MHC
    Yuko Ohta, Takashi Shiina, Rebecca L. Lohr · 2011 · The Journal of Immunology
  79. Genetic analysis of 19 X chromosome STR loci for forensic purposes in four Chinese ethnic groups
    Xingyi Yang, Xiaofang Zhang, Junyong Zhu et al. · 2017 · Scientific Reports
  80. No association or linkage between polymorphisms in the genes encoding cholecystokinin and the cholecystokinin B receptor and panic disorder
    Steven P. Hamilton, Susan L. Slager, LETICIA HELLEBY, Gary A. Heiman, Donald F. Klein, Susan E. Hodge, Myrna M. Weissman, Abby J. Fyer, James A. Knowles · 2000 · Molecular Psychiatry
  81. Effectiveness of alendronate treatment in postmenopausal women with osteoporosis: relationship with BsmI vitamin D receptor genotypes
    Stefano Palomba, Fabio Giuliano Numis, Giuseppe Mossetti · 2003 · Clinical Endocrinology
  82. A Tale of Two Genotypes: Consistency between Two High-Throughput Genotyping Centers
    Daniel E. Weeks, Yvette P. Conley, Robert E. Ferrell · 2002 · Genome Research
  83. Psychiatric Disorders in Clinical Genetics II: Individualizing Recurrence Risks
    J. Austin, Christina G. S. Palmer, B. Rosen-Sheidley, P. M. Veach, E. Gettig, H. Peay · 2008 · Journal of Genetic Counseling
  84. Genetic and functional association of FAM5C with myocardial infarction
    Jessica J. Connelly, Svati Hasmukh Shah, Jennifer F. Doss, Shera Gadson, Sarah C. Nelson, David R. Crosslin, A. Brent Hale, Xuemei Lou, Ty Wang, Carol S. Haynes et al. · 2008 · BMC Medical Genetics
  85. Contribution of the serotoninergic system to anxious and depressive traits that may be partially responsible for the phenotypical variability of bulimia nervosa
    Marta Ribasés, Fernando Fernández‐Aranda, Mónica Gratacòs, Josep Maria Mercader, Carolina Casasnovas, Araceli Núñez, Julio Vallejo, Xavier Estivill · 2006 · Journal of Psychiatric Research
  86. Consensus Genetic Maps as Median Orders from Inconsistent Sources
    B.N. Jackson, Patrick S. Schnable, Srinivas Aluru · 2008 · IEEE Transactions on Computational Biology and Bioinformatics
  87. Linkage analysis of chromosome 22q12–13 in a United Kingdom/Icelandic sample of 23 multiplex schizophrenia families
    Gursharan Kalsi, Jon Brynjolfsson, Robert J. Butler et al. · 1995 · American Journal of Medical Genetics
  88. An Immune Defect Causing Dominant Chronic Mucocutaneous Candidiasis and Thyroid Disease Maps to Chromosome 2p in a Single Family
    Thomas Prescott Atkinson, Alejandro A. Schäffer, Bodo Grimbacher, Harry W. Schroeder, Cristina Woellner, Christa S. Zerbe, Jennifer M. Puck · 2001 · The American Journal of Human Genetics
  89. Scheduling Mixed Workloads in Multi-grids: The Grid Execution Hierarchy
    Mark Silberstein, Dan Geiger, Assaf Schuster · 2006
  90. Genetic linkage methods for quantitative traits
    Christopher Ian Amos, Mariza de Andrade · 2001 · Statistical Methods in Medical Research
  91. Genetic susceptibility in familial melanoma from northeastern Italy
    Maria Teresa Landi, A M Goldstein, S Tsang, David J. Munroe, W Modi, Monica Ter‐Minassian, R Steighner, Michael C. Dean, N Metheny, Brian J Staats et al. · 2004 · Journal of Medical Genetics
  92. Identification of a Novel β-Cell Glucokinase (GCK) Promoter Mutation (−71G>C) That ModulatesGCKGene Expression Through Loss of Allele-Specific Sp1 Binding Causing Mild Fasting Hyperglycemia in Humans
    Daniela Gašperíková, Nicolas D. Tribble, Juraj Staník et al. · 2009 · Diabetes
  93. 20 Applications of neural networks for gene finding
    Andrea Sherriff, Jurg Ott · 2001 · Advances in genetics
  94. Asian population frequencies and haplotype distribution of killer cell immunoglobulin-like receptor (KIR) genes among Chinese, Malay, and Indian in Singapore
    Yi Chuan Lee, Soh Ha Chan, Ee Chee Ren · 2008 · Immunogenetics
  95. Homozygosity mapping of a third Joubert syndrome locus to 6q23
    Clotilde Lagier‐Tourenne, Eugen Boltshauser, Noralv Breivik, Moez Gribaa, Christine Bétard, Clara Barbot, Michel Koenig · 2004 · Journal of Medical Genetics
  96. Identification of a New Candidate Locus for Uric Acid Nephrolithiasis
    Maria Neve Ombra, Paola Forabosco, Stefania Casula, Andrea Angius, Gianbattista Maestrale, Enrico G. Petretto, Giuseppina Casu, Giacomo Colussi, Enzo Usai, Paola Maria Melis et al. · 2001 · The American Journal of Human Genetics
  97. (CCTTT)n repeat polymorphism in the NOS2 gene promoter is associated with atopy
    Satoshi Konno, Nobuyuki Hizawa, Etsuro Yamaguchi · 2001 · Journal of Allergy and Clinical Immunology
  98. A Survey of Affected-Sibship Statistics for Nonparametric Linkage Analysis
    Haydar Sengul, Daniel E. Weeks, Eleanor Feingold · 2001 · The American Journal of Human Genetics
  99. Genome‐wide linkage analysis for celiac disease in North American families
    Susan L. Neuhausen, Mike Feolo, Nicola J. Camp, James M. Farnham, Linda Sue Book, John J. Zone · 2002 · American Journal of Medical Genetics
  100. Susceptibility gene discovery for common metabolic and endocrine traits
    Mark I. McCarthy · 2002 · Journal of Molecular Endocrinology