Searching for genetic determinants in the new millennium

Cited by (1,000)

Items 601–700 of 1,000

1. A ComprehensiveIn SilicoAnalysis of the Functional and Structural Impact of SNPs in theIGF1RGene
   Sérgio Amorim de Alencar, Júlio César Dias Lopes · 2010 · BioMed Research International
2. Development and application of functional markers in maize
   Thomas Lübberstedt, Imad Zein, Jeppe Reitan Andersen, Gerhard Wenzel, Birte A. E. Krützfeldt, Joachim Eder, Milena Ouzunova, Chun Shi · 2005 · Euphytica
3. Association study of polymorphisms in the glutamate transporter genes SLC1A1, SLC1A3, and SLC1A6 with schizophrenia
   Xiangdong Deng, Hiroki Shibata, Naoko Takeuchi, Shinako Rachi, Mayumi Sakai, Hideaki Ninomiya, Nakao Iwata, Norio Ozaki, Yasuyuki Fukumaki · 2007 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
4. Immunogenetics in PSC
   Peter T. Donaldson, Suzanne Norris · 2001 · Best Practice & Research Clinical Gastroenterology
5. Chasing genes in Alzheimer?s and Parkinson?s disease
   Aida Maria Bertoli‐Avella, Ben A. Oostra, Peter Heutink · 2004 · Human Genetics
6. Association between the rs4880 superoxide dismutase 2 (C>T) gene variant and coronary heart disease in diabetes mellitus
   Danielle A Jones, Sarah L. Prior, Tricia S. Tang, Steve C Bain, Steven J. Hurel, Steve Eric Humphries, Jeffrey Wayne Stephens · 2010 · Diabetes Research and Clinical Practice
7. Germ‐line genetic variation of TP53 in osteosarcoma
   Sharon A. Savage, Laura A. Burdett, Rebecca J. Troisi, Chester W. Douglass, Robert N. Hoover, Stephen Jacob Chanock · 2006 · Pediatric Blood & Cancer
8. Deconstructing maize population structure
   Jonathan K. Pritchard · 2001 · Nature Genetics
9. Bayesian Haplotype Inference via the Dirichlet Process
   Eric P. Xing, Michael I. Jordan, Roded Sharan · 2007 · Journal of Computational Biology
10. Polymorphisms in the Two Helicases ERCC2/XPD and ERCC3/XPB of the Transcription Factor IIH Complex and Risk of Lung Cancer: A Case-Control Analysis in a Chinese Population
    Zhibin Hu, Liang Xu, Minhua Shao, Jing Yuan, Yi Wang, Feng Wang, Wentao Yuan, Ji Qian, Hongxia Ma, Ying Wang et al. · 2006 · Cancer Epidemiology Biomarkers & Prevention
11. Chromosome 4q25, Microsomal Transfer Protein Gene, and Human Longevity: Novel Data and a Meta-Analysis of Association Studies
    Marian Beekman, Gerard J. Blauw, Jeanine J. Houwing‐Duistermaat, Bernd Willem Brandt, Rudi G. J. Westendorp, P. Eline Slagboom · 2006 · The Journals of Gerontology Series A
12. High density linkage disequilibrium mapping using models of haplotype block variation
    Gideon Greenspan, Dan Geiger · 2004 · Bioinformatics
13. Population isolates: their special value for locating genes for bipolar disorder
    Michael Escamilla · 2001 · Bipolar Disorders
14. On the use of DNA pooling to estimate haplotype frequencies
    Shuang Wang, Kenneth K. Kídd, Hongyu Zhao · 2002 · Genetic Epidemiology
15. The Changing Face of Epidemiology in the Genomics Era
    R. Millikan · 2002 · Epidemiology
16. Genetic effects on susceptibility, clinical expression, and treatment outcome of type 1 autoimmune hepatitis
    Peter T. Donaldson, Albert J. Czaja · 2002 · Clinics in Liver Disease
17. Marker‐Assisted Gene Pyramiding for Cultivar Development
    Guoyou Ye, Kevin F. Smith · 2010 · Plant breeding reviews
18. Codon Usage Pattern of Genes Involved in Central Nervous System
    Arif Uddin, Supriyo Chakraborty · 2018 · Molecular Neurobiology
19. Effect of Population Stratification on Case-Control Association Studies
    Prakash Gorroochurn, Susan E. Hodge, Gary A. Heiman, David A. Greenberg · 2004 · Human Heredity
20. The search for complex disease genes: fault by linkage or fault by association?
    Miron Baron · 2001 · Molecular Psychiatry
21. Statistical Methods for the Analysis of Genetic Association Studies
    Guangyong Zou · 2005 · Annals of Human Genetics
22. Machine learning in schizophrenia genomics, a case‐control study using 5,090 exomes
    Yannis J Trakadis, Sameer Sardaar, Anthony Chen, Vanessa Fulginiti, Ankur Krishnan · 2018 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
23. Evidence for association of DNA sequence variants in the phosphatidylinositol-4-phosphate 5-kinase IIα gene (PIP5K2A) with schizophrenia
    Sibylle G. Schwab, Michael Knapp, Pamela B. Sklar, Gertrud Eckstein, C. Sewekow, Margitta Borrmann-Hassenbach, Margot Albus, Tim Becker, Joachim Franz Hallmayer, Bernard Lerer et al. · 2006 · Molecular Psychiatry
24. Statistical advances and challenges for analyzing correlated high dimensional SNP data in genomic study for complex diseases
    Yulan Liang, Arpad Kelemen · 2008 · Statistics Surveys
25. Recent development in genomic and proteomic research for asthma
    Eva Charlotte Halapi, Hakon H. Hakonarson · 2003 · Current Opinion in Pulmonary Medicine
26. Two-Stage Designs in Case–Control Association Analysis
    Yijun Zuo, Guohua Zou, Hongyu Zhao · 2006 · Genetics
27. The Autism Genome Project
    Diane Hu‐Lince, David Wesley Craig, Matthew J. Huentelman, Dietrich A. Stephan · 2005 · American Journal of PharmacoGenomics
28. The HapMap project and its application to genetic studies of drug response
    Panos Deloukas, D. R. Bentley · 2003 · The Pharmacogenomics Journal
29. Genetics of Atrial Fibrillation
    Steven A. Lubitz, B. Alexander Yi, Patrick T. Ellinor · 2010 · Heart Failure Clinics
30. Marker-assisted Gene Pyramiding for Inbred Line Development: Basic Principles and Practical Guidelines
    Guoyi Ye, F.S. Kevin · 2008
31. Analysis of multiple SNPs in genetic association studies: comparison of three multi‐locus methods to prioritize and select SNPs
    A. Geert Heidema, Edith J. M. Feskens, Pieter A. Doevendans, Henk J.T. Ruven, Hans C. van Houwelingen, Edwin C.M. Mariman, Jolanda M.A. Boer · 2007 · Genetic Epidemiology
32. Constraints for genetic association studies imposed by attributable fraction and familial risk
    Kari Hemminki, Justo Lorenzo Bermejo · 2006 · Carcinogenesis
33. Pharmacogenetics of cancer chemotherapy
    Jean Abraham, Helena Margaret Earl, Paul D.P. Pharoah, Carlos Caldas · 2006 · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer
34. Complexities in the genetic dissection of quantitative trait loci
    Ariel Darvasi, Anne Pisanté · 2002 · Trends in Genetics
35. A risk‐factor model of epistatic interaction, focusing on autism
    Marshall B. Jones, Péter Szatmári · 2002 · American Journal of Medical Genetics
36. A Fast Method for Computing High-Significance Disease Association in Large Population-Based Studies
    Gad Kimmel, Ron Shamir A · 2006 · The American Journal of Human Genetics
37. Candidate gene studies of bipolar disorder
    Jones, Ian, Craddock, Nick · 2001 · Annals of Medicine
38. Efficiency robust statistics for genetic linkage and association studies under genetic model uncertainty
    Jungnam Joo, Minjung Kwak, Zehua Chen, Gang Zheng · 2009 · Statistics in Medicine
39. Role Played by Human Mannose-Binding Lectin Polymorphisms in Pulmonary Tuberculosis
    Rosanna Capparelli, Marco Iannaccone, Daniela Palumbo, Chiara Medaglia, Emilio Moscariello, Alfredo Russo, Domenico Iannelli · 2009 · The Journal of Infectious Diseases
40. Phenotypic and genetic heterogeneity in a genome-wide linkage study of asthma families
    Janine Altmüller, Corinna Seidel, Young‐Ae Lee, Sabine Loesgen, Dieter Bulle, Frank Friedrichs, Heidemarie Jellouschek, Julika Kelber, Angela Keller, Antje Schuster et al. · 2005 · BMC Pulmonary Medicine
41. Association study of polymorphisms in the excitatory amino acid transporter 2 gene (SLC1A2) with schizophrenia
    Xiangdong Deng, Hiroki Shibata, Hideaki Ninomiya, Nobutada Tashiro, Nakao Iwata, Norio Ozaki, Yasuyuki Fukumaki · 2004 · BMC Psychiatry
42. Genetic risk factors for cerebrovascular disease in children with sickle cell disease: design of a case-control association study and genomewide screen
    Gaye T Adams, Harold Snieder, Virgil C McKie, Betsy Clair, Donald J. Brambilla, Robert J. Adams, F. Kutlar, Abdullah Kutlar · 2003 · BMC Medical Genetics
43. Human blood genomics: distinct profiles for gender, age and neurofibromatosis type 1
    Yang Tang, Aigang Lu, Ruiqiong Ran, Bruce J. Aronow, Elizabeth K. Schorry, Robert James Hopkin, Donald L. Gilbert, Tracy A. Glauser, Andrew D. Hershey, Neil W. Richtand et al. · 2004 · Molecular Brain Research
44. Experimental Designs for Reliable Detection of Linkage Disequilibrium in Unstructured Random Population Association Studies
    Roderick D. Ball · 2005 · Genetics
45. Gene prioritization and clustering by multi-view text mining
    Shi Qi Yu, Léon-Charles Tranchevent, Bart De Moor, Yves Moreau · 2010 · BMC Bioinformatics
46. Increased Risk of Complex Regional Pain Syndrome in Siblings of Patients?
    Annetje M. De Rooij A, Marissa de Mos, Jacobus Johannes van Hilten, Miriam Sturkenboom, Maria Florencia Gosso, Arn M.J.M. van den Maagdenberg, Johan Marinus · 2009 · Journal of Pain
47. Effect of Population Stratification on Case-Control Association Studies
    Gary A. Heiman, Susan E. Hodge, Prakash Gorroochurn, Junying Zhang, David A. Greenberg · 2004 · Human Heredity
48. Non-major-histocompatibility-complex genetics of ankylosing spondylitis
    M BROWNMBBSMDFRACP · 2006 · Best Practice & Research Clinical Rheumatology
49. Backward Genotype-Trait Association (BGTA)-Based Dissection of Complex Traits in Case-Control Designs
    Tian Zheng, Hui Wang, Shaw‐Hwa Lo · 2006 · Human Heredity
50. Genetic Variation associated with Ischemic Heart Failure: A HuGE Review and Meta-Analysis
    Georgios D. Kitsios, Elias Zintzaras · 2007 · American Journal of Epidemiology
51. Polymorphisms in the epidermal growth factor receptor gene and the risk of primary lung cancer: a case-control study
    Jin Eun Choi, Sun Ha Park, Kyung Mee Kim, Won Kee Lee, Sin Kam, Sung Ick, Chang Ho Kim, Young Mo Kang, Youngchul Kim, Sung Beom Han et al. · 2007 · BMC Cancer
52. Association of ApoE genetic variants with obstructive sleep apnea in children
    Maninder Kalra, Prodipto Pal, Ritesh D. Kaushal, Raouf Samy Amin, Lawrence M. Dolan, Kelly Fitz, Sunil Kumar, Xiaohua Sheng, Saurav Guha, Joydeep Mallik et al. · 2007 · Sleep Medicine
53. Interleukin–6 ( IL-6 ) rs1800796 and cyclin dependent kinase inhibitor ( CDKN2A/CDKN2B ) rs2383207 are associated with ischemic stroke in indigenous West African Men
    Rufus Akinyemi, Donna K. Arnett, Hemant K. Tiwari, Bruce I Ovbiagele, Fred Stephen Sarfo, Vinodh Srinivasasainagendra, Marguerite R. Irvin, Abiodun Moshood Adeoye, Rodney T. Perry, Albert Kwaku Akpalu et al. · 2017 · Journal of the Neurological Sciences
54. The evolution of pharmaceutical innovation
    Paul Nightingale, Surya Mahdi · 2006 · Cambridge University Press eBooks
55. Hierarchical decision tree induction in distributed genomic databases
    Amir Bar-Or, Daniel Keren, Assaf Schuster, Ran Wolff · 2005 · IEEE Transactions on Knowledge and Data Engineering
56. D2S2944 identifies a likely susceptibility locus for recurrent, early-onset, major depression in women
    George S. Zubenko, Hugh B. Hughes, J. Scott Stiffler, Wendy N. Zubenko, Barry B. Kaplan · 2002 · Molecular Psychiatry
57. Multiple hypothesis testing strategies for genetic case–control association studies
    Philip S. Rosenberg, Anney Che, Bingshu E. Chen · 2005 · Statistics in Medicine
58. Gene–environment interactions on the risk of esophageal cancer among Asian populations with the G48A polymorphism in the alcohol dehydrogenase-2 gene: a meta-analysis
    Long Zhang, Yingjiu Jiang, Qingcheng Wu, Qiang Li, Dan Chen, Ling Xu, Cheng Zhang, Min Zhang, Ling Ye · 2014 · Tumor Biology
59. Association of interleukin‐10 gene promoter polymorphisms with chronic and aggressive periodontitis
    SM Jaradat, Khansa Taha Ababneh, Saied A. Jaradat, MS Abbadi, AH Taha, JA Karasneh, Hazem I. Haddad · 2011 · Oral Diseases
60. Association of the catechol-O-methyltransferase polymorphism with methylphenidate response in a classroom setting in children with attention-deficit hyperactivity disorder
    Keun-Ah Anna Cheon, Jin-Yong Jun, Dae-Yeon Cho · 2008 · International Clinical Psychopharmacology
61. The Future of Genetics and Genomics
    Calum A. MacRae, Ramachandran Srini Vasan · 2016 · Circulation
62. Association analysis of physicochemical traits on eating quality in rice (Oryza sativa L.)
    Wei-Guo Zhao, Jong‐Wook Chung, Soon-Wook Kwon, Jeong-Heui Lee, Kyung‐Ho Ma, Yong‐Jin Park · 2012 · Euphytica
63. Detecting multiple associations in genome-wide studies
    Frank Dudbridge, Arief Gusnanto, Bobby P.C. Koeleman · 2006 · Human Genomics
64. Role of host genes in sporadic gastric cancer
    Emad M. El-Omar · 2006 · Best Practice & Research Clinical Gastroenterology
65. Approaches to gene mapping in complex disorders and their application in child psychiatry and psychology
    Philip J. Asherson, Sarah R Curran · 2001 · The British Journal of Psychiatry
66. Polymorphism of human mu class glutathione transferases
    Natasha Tetlow, Anna Robinson, TIM MANTLE, Philip G. Board · 2004 · Pharmacogenetics
67. Searching for Type 2 Diabetes Genes in the Post-genome Era
    M. Alan Permutt, Andrew Tym Hattersley · 2000 · Trends in Endocrinology and Metabolism
68. Genetic analysis of multiple sclerosis
    Alastair Compston, Stephen J. Sawcer · 2002 · Current Neurology and Neuroscience Reports
69. The genes for schizophrenia: Finally a breakthrough?
    Brian H. Shirts, Vishwajit Laxmikant Nimgaonkar · 2004 · Current Psychiatry Reports
70. Applied genomics: integration of the technology within pharmaceutical research and development
    Mark I. Cockett, Nicholas C. Dracopoli, Elliott Sigal · 2000 · Current Opinion in Biotechnology
71. Susceptibility gene discovery for common metabolic and endocrine traits
    Mark I. McCarthy · 2002 · Journal of Molecular Endocrinology
72. Snagger: A user-friendly program for incorporating additional information for tagSNP selection
    Christopher K. Edlund, Won H. Lee, Dalin Li, David Van Den Berg, David V. Conti · 2008 · BMC Bioinformatics
73. Custom genotyping for substance addiction susceptibility genes in Jordanians of Arab descent
    Laith Naser AL-Eitan, Saied A. Jaradat, Gary Kenneth Hulse, Guan K. Tay · 2012 · BMC Research Notes
74. Familial risks for common diseases: Etiologic clues and guidance to gene identification
    Kari Hemminki, Xinjun Li, Kristina Sundquist, Jan Sundquist · 2008 · Mutation Research/Reviews in Mutation Research
75. HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer
    Patrick R. Benusiglio, Paul D.P. Pharoah, Paula L. Smith, Fabienne Lesueur, Don M. Conroy, Robert Luben, G Dew, Cally Jordan, Alison M. Dunning, Douglas F. Easton et al. · 2006 · British Journal of Cancer
76. Polymorphism in genes involved in adrenergic signaling associated with Alzheimer’s
    Maria Jesus Bullido, María C. Ramos, Ana Ruiz‐Gómez, Antonio S. Tutor, Isabel Sastre, Ana Frank, Francisco Coria, Pedro Gil, Federico Mayor, Fernando Valdivieso · 2003 · Neurobiology of Aging
77. A Field Synopsis and Meta-Analysis of Genetic Association Studies in Peripheral Arterial Disease: The CUMAGAS-PAD Database
    Elias Zintzaras, Nikos Zdoukopoulos · 2009 · American Journal of Epidemiology
78. Polymorphisms in thehMSH2Gene and the Risk of Primary Lung Cancer
    Chi Young Jung, Jin Eun Choi, Jung Min Park, Myung Hwa Chae, Hyo‐Gyoung Kang, Kyung Mee Kim, Su Jeong Lee, Won Kee Lee, Sin Kam, Seung Ick et al. · 2006 · Cancer Epidemiology Biomarkers & Prevention
79. Molecular diagnostics in monogenic and multifactorial forms of Type 2 diabetes
    Mark I. McCarthy, Andrew Tym Hattersley · 2001 · Expert Review of Molecular Diagnostics
80. Single Nucleotide Polymorphisms Associated with Hepatocellular Carcinoma in Patients with Chronic Hepatitis B Virus Infection
    Yoon Jun Kim, Hyo-Suk Lee · 2005 · Intervirology
81. Functional polymorphism in the promoter region of the gelatinase B gene in relation to coronary artery disease and restenosis after percutaneous coronary intervention
    Hyun‐Jung Cho, In‐Ho Chae, K.-W. Park, J.-R. Ju, Seil Oh, M.-M. Lee, Y.-B. Park · 2002 · Journal of Human Genetics
82. Nuts and bolts of psychiatric genetics: building on the Human Genome Project
    Kathryn Louise Evans, David John Porteous, Walter J Muir, Douglas Blackwood · 2001 · Trends in Genetics
83. 4G/5G Plasminogen Activator Inhibitor-1 Polymorphisms and Haplotypes Are Associated with Pneumonia
    Sachin P. Yende, Derek C. Angus, Jingzhong Ding, Anne B. Newman, John A. Kellum, Rongling Li, Robert E. Ferrell, Joseph M. Zmuda, Stephen B. Kritchevsky, Tamara B. Harris et al. · 2007 · American Journal of Respiratory and Critical Care Medicine
84. Endothelial Nitric Oxide Synthase Polymorphisms and Haplotypes in Amerindians
    Marcelo R. Luizon, Tatiane C. Izidoro‐Toledo, Aguinaldo Luíz Simões, José Eduardo Tanus-Santos · 2009 · DNA and Cell Biology
85. Host genetic studies in adult pulmonary tuberculosis
    Christian G. Meyer, Thorsten Thye · 2014 · Seminars in Immunology
86. Role of host genetics in fibrosis
    Georgina Louise Hold, Paraskevi Untiveros, Karin A. Saunders, Emad M. El-Omar · 2009 · Fibrogenesis & Tissue Repair
87. A classical likelihood based approach for admixture mapping using EM algorithm
    Xiaofeng Zhu, Shuanglin Zhang, Hua Tang, Richard Cooper · 2006 · Human Genetics
88. Association between human African trypanosomiasis and the IL6 gene in a Congolese population
    David Courtin, Jacqueline Milet, Vincent Jamonneau, Claude Sese, Victor Kande Betu Kumeso, Constantin Miaka Mia Bilenge, Christine Bétard, André Garcia · 2006 · Infection Genetics and Evolution
89. Expansion and diversification of KRAB zinc-finger genes within a cluster including Regulator of sex-limitation 1 and 2
    Christopher J. Krebs, Leslie K. Larkins, Shaema M. Khan, Diane M. Robins · 2005 · Genomics
90. The search for genenotype/phenotype associations and the phenome scan
    Richard Wyn Jones, Marcus E Pembrey, Jean Golding, David Herrick · 2005 · Paediatric and Perinatal Epidemiology
91. Human Pharmacogenomic Variations and Their Implications for Antifungal Efficacy
    Joseph Meletiadis, Stephen Jacob Chanock, Thomas J. Walsh · 2006 · Clinical Microbiology Reviews
92. Family‐based and population study of a functional promoter‐region monoamine oxidase A polymorphism in autism: Possible association with IQ
    Nurit Yirmiya, Tammy Pilowsky, Tidhar Sigal, Lubov Nemanov, Larissa Altmark, Richard P. Ebstein · 2002 · American Journal of Medical Genetics
93. Quantitative-Trait Loci on Chromosomes 1, 2, 3, 4, 8, 9, 11, 12, and 18 Control Variation in Levels of T and B Lymphocyte Subpopulations
    Margaret A. Hall, Paul J. Norman, Bonnie Thiel, Hemant K. Tiwari, Andy P. Peiffer, R.W. Vaughan, Stephen M. Prescott, Mark Leppert, Nicholas J. Schork, Jerry S. S. Lanchbury · 2002 · The American Journal of Human Genetics
94. Genetics and Etiopathophysiology of Schizophrenia
    Janet L. Sobell, Marci J. Mikesell, Cynthia T. McMurray · 2002 · Mayo Clinic Proceedings
95. Genetic Associations in Preterm Birth: A Primer of Marker Selection, Study Design, and Data Analysis
    Ramkumar Menon, Stephen J. Fortunato, Poul Thorsen, Scott M. Williams · 2006 · Journal of the Society for Gynecologic Investigation
96. Association of melanogenesis genes with skin color variation among Japanese females
    Yuko Abe, Gen Tamiya, Tomohiro Nakamura, Yutaka Hozumi, Tamio Suzuki · 2012 · Journal of Dermatological Science
97. Single Nucleotide Polymorphisms and Cancer Susceptibility
    Richard A Hubner, Richard S. Houlston · 2016 · Springer eBooks
98. Acute lung injury and the coagulation pathway: potential role of gene polymorphisms in the protein C and fibrinolytic pathways
    Anil Sapru, Joseph Leo Wiemels, John S. Witte, Lorraine B. Ware, Michael A. Matthay · 2006 · Intensive Care Medicine
99. Type 1 diabetes risk analysis on dried blood spot samples from population‐based newborns: design and feasibility of an unselected case–control study
    Stefanie Eising, Jannet Svensson, Kristin Skogstrand, Anita Nilsson, Kristian Francis Lynch, Paal Skytt Andersen, Åke Lernmark, DAVID MICHAEL HOUGAARD, Flemming Pociot, Bent Nørgaard‐Pedersen et al. · 2007 · Paediatric and Perinatal Epidemiology
100. A SCIENCE OF THE INDIVIDUAL: Implications for a Medical School Curriculum
     Barton Childs, Charles Wiener, David L. Valle · 2005 · Annual Review of Genomics and Human Genetics