A General Test of Association for Quantitative Traits in Nuclear Families
Abecasis, G.R., Cardon, L.R., Cookson, W.O.C.·2000·The American Journal of Human Genetics
DOI 10.1086/302698
Cited by (1,000)
Items 201–300 of 1,000
- Ovarian Morphology Is a Marker of Heritable Biochemical Traits in Sisters with Polycystic OvariesStephen Franks, Lisa J. Webber, Micaela J. Goh, Anne Valentine, Davinia M. White, Gerard S. Conway, Steven Wiltshire, Mark I. McCarthy · 2008 · The Journal of Clinical Endocrinology & Metabolism
- Genetic influences on quantity of alcohol consumed by adolescents and young adultsChristian Jean Hopfer, David S. Timberlake, Brett C. Haberstick, Jeffrey M. Lessem, Marissa A. Ehringer, Andrew Smolen, John K. Hewitt · 2004 · Drug and Alcohol Dependence
- Molecular genetics of essential hypertension: recent results and emerging strategiesDavid S. Timberlake, Daniel T. O’Connor, Robert J. Parmer · 2001 · Current Opinion in Nephrology & Hypertension
- The ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligenceNitzan Mekel-Bobrov, Danielle Posthuma B, Sandra L. Gilbert, Penelope A. Lind, Maria Florencia Gosso, Michelle Luciano A, Sarah E. Harris, Timothy Charles Bates, Tinca J. C. Polderman, Lawrence J. Whalley et al. · 2007 · Human Molecular Genetics
- Role of the cholinergic muscarinic 2 receptor (CHRM2) gene in cognitionDavid E. Comings, Shijuan Wu, Massud Rostamkhani, Matt K. McGue, William G. lacono, Li-Tzong Cheng, James P. MacMurray · 2003 · Molecular Psychiatry
- Genetic linkage and association between chromosome 1q and working memory function in schizophreniaTimothy L. Gasperoni, Jesper Ekelund, MATTI O. HUTTUNEN, Christina G.S. Palmer, Annamari Tuulio‐Henriksson, Jouko K Lönnqvist, Jaakko A. Kaprio, Leena Peltonen, Tyrone D. Cannon · 2002 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- The inheritance of intermediate phenotypes for schizophreniaTyrone D. Cannon · 2005 · Current Opinion in Psychiatry
- Genetic Analysis of 103 Candidate Genes for Coronary Artery Disease and Associated Phenotypes in a Founder Population Reveals a New Association between Endothelin-1 and High-Density Lipoprotein CholesterolGuillaume Paré, David Serre, Diane Brisson, Sonia Savitri Anand, Alexandre Montpetit, Gérald Tremblay, James C. Engert, Thomas J. Hudson, Daniel Gaudet · 2007 · The American Journal of Human Genetics
- Significant correlation in linkage signals from genome-wide scans of schizophrenia and schizotypyAyman H. Fanous, Michael Churton Neale, C O Gardner, Bradley Todd Webb, Richard E. Straub, F. Anthony O’Neill, Dermot Walsh, Brien P. Riley, Kenneth S. Kendler · 2007 · Molecular Psychiatry
- Dysbindin (DTNBP1, 6p22.3) is Associated with Childhood-Onset Psychosis and Endophenotypes Measured by the Premorbid Adjustment Scale (PAS)Michele Caroline Gornick, Anjene Musick Addington, Alexandra L. Sporn, Nitin Gogtay, DEANNA K. GREENSTEIN, Marge Lenane, Peter Gochman, Anna E. Ordóñez, Rishi Balkissoon, Radhakrishna Vakkalanka et al. · 2005 · Journal of Autism and Developmental Disorders
- Identification of common genetic variants that account for transcript isoform variation between human populationsWei Zhang, Shiwei Duan, Wasim Kamel Bleibel, Steven A. Wisel, R. Stephanie Huang, Xiaolin Wu, Lijun He, Tyson A. Clark, Tina X. Chen, Anthony C. Schweitzer et al. · 2008 · Human Genetics
- Neuromedin β: a strong candidate gene linking eating behaviors and susceptibility to obesityLuigi Bouchard, Vicky Drapeau, Véronique Provencher, Simone Lemieux, Yvon C. Chagnon, Treva Rice, D. C. Rao, Marie‐Claude Vohl, Angelo Tremblay, Claude Bouchard et al. · 2004 · American Journal of Clinical Nutrition
- Haplotype Combinations of Calpain 10 Gene Polymorphisms Associate With Increased Risk of Impaired Glucose Tolerance and Type 2 Diabetes in South IndiansPaul G. Cassell, Alan E. Jackson, Bernard V. North, Julie Evans, Denise Syndercombe‐Court, Christopher Phillips, Ambady Ramachandran, Chamukuttan Snehalatha, Susan V. Gelding, Shanti Vijayaravaghan et al. · 2002 · Diabetes
- Population-specific genetic variants important in susceptibility to cytarabine arabinoside cytotoxicityChristine Mary Hartford, Shiwei Duan, Shannon M. Delaney, Shuangli Mi, Emily O. Kistner, Jatinder Kaur Lamba, R. Stephanie Huang, Mary Eileen Dolan · 2008 · Blood
- Genetic Mapping Populations for Conducting High-Resolution Trait Mapping in PlantsJames Cockram, Ian Mackay · 2018 · Advances in biochemical engineering, biotechnology
- Association Between Genes of Disrupted in Schizophrenia 1 (DISC1) Interactors and Schizophrenia Supports the Role of the DISC1 Pathway in the Etiology of Major Mental IllnessesLiisa Tomppo, William Hennah, Päivi Lahermo, Anu Loukola, Annamari Tuulio‐Henriksson, Jaana Suvisaari, Timo Partonen, Jesper Ekelund, Jouko K Lönnqvist, Leena Peltonen · 2009 · Biological Psychiatry
- Heritability and Genome-Wide Linkage in US and Australian Twins Identify Novel Genomic Regions Controlling Chromogranin ADaniel T. O’Connor, Gu Zhu, Fangwen Rao, Laurent Taupenot, Maple M. Fung, Madhusudan Das, Sushil Kumar Mahata, Manjula Mahata, Lei Wang, Kuixing Zhang et al. · 2008 · Circulation
- Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutationTimothy Charles Bates, Penelope A. Lind, Michelle Luciano A, Grant W. Montgomery, Nicholas G. Martin, Margaret J. Wright · 2009 · Molecular Psychiatry
- Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophreniaChen, Pei-Lung, Avramopoulos, Dimitrios, Lasseter, Virginia K., McGrath, John A., Fallin, M. Daniele, Liang, Kung-Yee, Nestadt, Gerald, Feng, Ningping, Steel, Gary, Cutting, Andrew S. et al. · 2009 · The American Journal of Human Genetics
- Significant associations of stearoyl-CoA desaturase ( SCD1 ) gene with fat deposition and composition in skeletal muscleZhihua Jiang, Jennifer J. Michal, David J. Tobey, Tyler F. Daniels, Daniel Clark Rule, Michael D. MacNeil · 2008 · International Journal of Biological Sciences
- Genome Wide Association Identifies PPFIA1 as a Candidate Gene for Acute Lung Injury Risk Following Major TraumaJason D. Christie, Mark M. Wurfel, Rui Feng, Grant Edward O’Keefe, Jonathan P. Bradfield, Lorraine B. Ware, David C. Christiani, Carolyn S. Calfee, Mitchell J M Cohen, Michael A. Matthay et al. · 2012 · PLoS ONE
- Evidence that single nucleotide polymorphism in the uncoupling protein 3 (UCP3) gene influences fat distribution in women of European and Asian originP. G. Cassell, P. J. Saker, Stewart J. Huxtable, Eleni Κousta, A. E. Jackson, Andrew Tym Hattersley, Timothy M. Frayling, Mark Walker, Peter G Kopelman, A. Ramachandran et al. · 2000 · Diabetologia
- Using the Noninformative Families in Family-Based Association Tests: A Powerful New Testing StrategyChristoph Lange, Dawn Lisa DeMeo, Edwin K. Silverman, Scott T. Weiss, Nan M. Laird · 2003 · The American Journal of Human Genetics
- Leptin Is Associated With Blood Pressure and Hypertension in Women From the National Heart, Lung, and Blood Institute Family Heart StudyDuanduan Ma, Mary Furlan Feitosa, Jemma B. Wilk, Jason M. Laramie, Kai F. Yu, Catherine Leiendecker‐Foster, Richard H. Myers, Michael A. Province, Ingrid B. Borecki · 2009 · Hypertension
- β2-Adrenergic receptor polymorphisms: pharmacogenetic response to bronchodilator among African American asthmaticsHui‐Ju Tsai, Nishat Shaikh, Jennifer Y. Kho, Natalie C. Battle, Mariam Naqvi, Daniel Navarro, Henry Matallana, Craig M. Lilly, Celeste S. Eng, Gunjan Kumar et al. · 2006 · Human Genetics
- The bipolar disorder phenome database: a resource for genetic studiesPotash, James B., Toolan, Jennifer, Steele, Jo, Miller, Erin B., Pearl, Justin, Zandi, Peter P., Schulze, Thomas G., Kassem, Layla, Simpson, Sylvia G., Lopez, Victor et al. · 2007 · American Journal of Psychiatry
- Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population samplePenelope A. Lind, Michelle Luciano A, Margaret J. Wright, Grant W. Montgomery, Nicholas G. Martin, Timothy Charles Bates · 2010 · European Journal of Human Genetics
- Genome-wide association study identifies three key loci for high mesocarp oil content in perennial crop oil palmChee-Keng Teh, Ai Ling Ong, Qi-Bin Kwong, Sukganah Apparow, Fook Tim Chew, Sean Mayes, Mohaimi Mohamed, David R. Appleton, Harikrishna Kulaveerasingam · 2016 · Scientific Reports
- Interpreting population- and family-based genome-wide association studies in the presence of confoundingCarl Veller, Graham Coop · 2024 · PLoS Biology
- Association of Sirtuin 1 (SIRT1) Gene SNPs and Transcript Expression Levels With Severe ObesityStephen J. Clark, Mario Falchi, Bob Olsson, Peter Jacobson, Stéphane Cauchi, Beverley Balkau, Michel Marre, Olivier Lantieri, Johanna C. Andersson‐Assarsson, Margareta Jernås et al. · 2011 · Obesity
- Identification of Risk and Age-at-Onset Genes on Chromosome 1p in Parkinson DiseaseSofia A. Oliveira, Yi‐Ju Li, Maher Noureddine, Stephan L. Zuchner, Xuejun Qin, Margaret Ann Pericak‐Vance, Jeffery M. Vance · 2005 · The American Journal of Human Genetics
- Haplotype-Based Localization of an Alcohol Dependence Gene to the 5q34 γ-Aminobutyric Acid Type A Gene ClusterMarta Radel, Roger L. Vallejo, Nakao Iwata, Richard Aragon, Jeffrey C. Long, Matti E. Virkkunen, David A Goldman · 2005 · Archives of General Psychiatry
- Family‐Based Methods for Linkage and Association AnalysisNan M. Laird, Christoph Lange · 2008 · Advances in genetics
- Family-Based Genome-Wide Association StudiesBeben Benyamin, Peter M. Visscher, Allan F. McRae · 2009 · Pharmacogenomics
- A Statistical Approach for Testing Cross-Phenotype Effects of Rare VariantsK. Alaine Broadaway, David J. Cutler, Richard Duncan, Jacob L. Moore, Erin Bakshis Ware, Min A. Jhun, Lawrence F. Bielak, Wei Zhao, Jennifer A. Smith, Patricia A. Peyser et al. · 2016 · The American Journal of Human Genetics
- Genome-Wide Association Study Reveals Natural Variations Contributing to Drought Resistance in CropsHongwei Wang, Feng Qin · 2017 · Frontiers in Plant Science
- Family-based association studiesHongyu Zhao · 2000 · Statistical Methods in Medical Research
- Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1William Hennah, Liisa Tomppo, Tero Hiekkalinna, Outi M. Palo, Helena Kilpinen, Jesper Ekelund, Annamari Tuulio‐Henriksson, Kaisa Silander, Timo Partonen, Tiina Paunio et al. · 2006 · Human Molecular Genetics
- Methylation and QTDT analysis of the 5-HT2A receptor 102C allele: Analysis of suicidality in major psychosisVincenzo De Luca, Emanuela Viggiano, Ranbir Dhoot, James L. Kennedy, Albert H.C. Wong · 2008 · Journal of Psychiatric Research
- Association genetics of chemical wood properties in black poplar (Populus nigra)Fernando P. Guerra, Jill Wegrzyn, Robert W. Sykes, Mark F. Davis, Brian J. Stanton, David B. Neale · 2012 · New Phytologist
- Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosisLi, Yi-Ju, Pericak-Vance, Margaret A., Haines, Jonathan L., Siddique, Nailah, McKenna-Yasek, Diane, Hung, Wu-Yen, Sapp, Peter, Allen, Coy I., Chen, Wenjie, Hosler, Betsy et al. · 2004 · Neurogenetics
- Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson diseaseNoureddine, Maher A., Qin, Xue-Jun, Oliveira, Sofia A., Skelly, Tara J., van der Walt, Joelle, Hauser, Michael A., Pericak-Vance, Margaret A., Vance, Jeffery M., Li, Yi-Ju · 2005 · Human Genetics
- Common Polymorphisms in the Promoter of the Visfatin Gene (PBEF1) Influence Plasma Insulin Levels in a French-Canadian PopulationSwneke Donovan Bailey, J. Concepción Loredo‐Osti, Pierre Lepage, Janet Faith, Joelle Fontaine, Katia Desbiens, Thomas J. Hudson, Claude Bouchard, Daniel Gaudet, Louis Përusse et al. · 2006 · Diabetes
- Genome-Wide Association Study of the Child Behavior Checklist Dysregulation ProfileMick, Eric, McGough, James, Loo, Sandra, Doyle, Alysa E., Wozniak, Janet, Wilens, Timothy E., Smalley, Susan, McCracken, James, Biederman, Joseph, Faraone, Stephen V. · 2011 · Journal of the American Academy of Child & Adolescent Psychiatry
- Association of the Serotonin Transporter Gene With Smoking BehaviorKremer, Ilana, Bachner-Melman, Rachel, Reshef, Alon, Broude, Leonid, Nemanov, Lubov, Gritsenko, Inga, Heresco-Levy, Uriel, Elizur, Yoel, Ebstein, Richard P. · 2005 · American Journal of Psychiatry
- Whole-genome association study for fatty acid composition of oleic acid in Japanese Black cattleYoshinobu Uemoto, Tsuyoshi Abe, N. Tameoka, Hiroyuki HASEBE, Keiichi Inoue, Hideto Nakajima, N. Shoji, Masato Kobayashi, E. Kobayashi · 2010 · Animal Genetics
- Leptin and Leptin Receptor Gene Polymorphisms and Changes in Glucose Homeostasis in Response to Regular Exercise in Nondiabetic IndividualsTimo Antero Lakka, Tuomo Rankinen, Stanley John Weisnagel, Yvon C. Chagnon, Hanna-Maaria Lakka, Olavi H. Ukkola, Normand G. Boulé, Treva Rice, Arthur S. Leon, James S. Skinner et al. · 2004 · Diabetes
- PBAT: A comprehensive software package for genome-wide association analysis of complex family-based studies.Van Steen, Kristel, Lange, Christoph · 2005 · Human Genomics
- Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure ProgramGeorg Ehret, Alanna C. Morrison, Ashley O’Connor, Megan L. Grove, Lisa Morrison Baird, Karen Schwander, Alan B. Weder, Richard Cooper, D. C. Rao, Steven C. Hunt et al. · 2008 · European Journal of Human Genetics
- TNF as a malaria candidate gene: polymorphism-screening and family-based association analysis of mild malaria attack and parasitemia in Burkina FasoLaurence Flori, Nicolas F. Delahaye, F. Iraqi, Maria Hernandez-Valladares, Francis Fumoux, Pascal Rihet · 2005 · Genes and Immunity
- GWAS analysis of QTL for enteric septicemia of catfish and their involved genes suggest evolutionary conservation of a molecular mechanism of disease resistanceTao Zhou, Shikai Liu, Xin Geng, Yulin Jin, J Chen, Lisui Bao, Jun Yao, Yu Zhang, Jiaren Zhang, Luyang Sun et al. · 2016 · Molecular Genetics and Genomics
- Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1Clyde Francks, Simon E. Fisher, Richard K. Olson, Bruce F. Pennington, Shelley D. Smith, John C. DeFries, Anthony P. Monaco · 2002 · Psychiatric Genetics
- Heritability of MRI Lesion Volume in CADASILChristian Opherk, Nils Peters, Markus Holtmannspötter, Andreas Gschwendtner, Bertram Müller‐Myhsok, Martin Dichgans · 2006 · Stroke
- An assessment of gene‐by‐environment interactions in developmental dyslexia‐related phenotypesS. Mascheretti, Alexandre Bureau, M. Battaglia, D. Simone, E. Quadrelli, Jordie Croteau, M. R. Cellino, R. Giorda, S. Beri, M. Maziade et al. · 2012 · Genes, Brain and Behavior
- Association Between Common Polymorphisms of the Proopiomelanocortin Gene and Body Fat DistributionMichelle Baker, Nicole Gaukrodger, Bongani M. Mayosi, Helen Imrie, Martin Farrall, Hugh C Watkins, John Connell, Peter J Avery, Bernard D. Keavney · 2005 · Diabetes
- Genetic Variants Contributing to Daunorubicin-Induced CytotoxicityR. Stephanie Huang, Shiwei Duan, Emily O. Kistner, Wasim Kamel Bleibel, Shannon M. Delaney, Donna Lee Fackenthal, Soma Das, Mary Eileen Dolan · 2008 · Cancer Research
- A Genome-Wide Scan for Carotid Artery Intima-Media ThicknessDai Wang, Huiying Yang, Manuel J. Quiñones, Isabel Bulnes‐Enriquez, Xochitl Jimenez, Roxana De La Rosa, Tamara Modilevsky, K.-H. Yu, Yanjie Li, Kent D. Taylor et al. · 2005 · Stroke
- Human ALOX12, but Not ALOX15, Is Associated With BMD in White Men and WomenShoji Ichikawa, Daniel L. Koller, Michelle L. Johnson, Dongbing Lai, Xiaoling Xuei, Howard J. Edenberg, Robert F. Klein, ERIC S. ORWOLL, Siu Lui Hui, Tatiana Foroud et al. · 2006 · Journal of Bone and Mineral Research
- A Genome-Wide Association Study Identifies Multiple Regions Associated with Head Size in CatfishXin Geng, Shikai Liu, Jun Yao, Lisui Bao, Jiaren Zhang, Chao Li, Ruijia Wang, Jin Sha, Peng Zeng, Degui Zhi et al. · 2016 · G3 Genes Genomes Genetics
- Determinants and Upper-Limit Heritabilities of Skeletal Muscle Mass and StrengthWim Huygens, Martine A. Thomis, Maarten Peeters, ROBERT F. VLIETINCK, Gaston Prudence Beunen · 2004 · Canadian Journal of Applied Physiology
- Heritability estimation and differential analysis of count data with generalized linear mixed models in genomic sequencing studiesShiquan Sun, Jiaqiang Zhu, Sahar V. Mozaffari, Carole Ober, Mengjie Chen, Xiang Zhou · 2018 · Bioinformatics
- Parental Phenotypes in Family-Based Association AnalysisShaun Purcell, Pak Chung Sham, Mark J. Daly · 2005 · The American Journal of Human Genetics
- Linkage of myostatin pathway genes with knee strength in humansWim Huygens, Martine A. Thomis, Maarten Peeters, Jeroen Aerssens, Rob G. J. H. Janssen, ROBERT F. VLIETINCK, Gaston Prudence Beunen · 2004 · Physiological Genomics
- Common haplotypes in five genes influence genetic variance of LDL and HDL cholesterol in the general populationHans Knoblauch · 2002 · Human Molecular Genetics
- A Single Nucleotide Polymorphism Fine Mapping Study of Chromosome 1q42.1 Reveals the Vulnerability Genes for Schizophrenia, GNPAT and DISC1: Association with Impairment of Sustained AttentionYu‐Li Liu, Cathy S.J. Fann, Chih‐Min Liu, Wei J. Chen, Jer‐Yuarn Wu, Wen‐Hung Chung, Chun‐Houh Chen, Yuh‐Shan Jou, Shih-Kai Liu, Tzung‐Jeng Hwang et al. · 2006 · Biological Psychiatry
- Association between quantitative traits underlying asthma and the HLA-DRB1 locus in a family-based population sampleMiriam F. Moffatt, Carsten Schou, Jennifer A. Faux, Gonçalo R. Abecasis, Alan James, Arthur William Musk, William Cookson · 2001 · European Journal of Human Genetics
- Evaluation of record linkage between a large healthcare provider and the Utah Population DatabaseScott L. DuVall, Alison M. Fraser, Kerry G. Rowe, Alun Thomas, Geraldine P. Mineau · 2011 · Journal of the American Medical Informatics Association
- Left Ventricular Mass in Relation to Genetic Variation in Angiotensin II Receptors, Renin System Genes, and Sodium ExcretionTatiana Kuznetsova, Jan A. Staessen, Lutgarde Thijs, Christiane Kunath, Agnieszka Olszanecka, Andrew N. Ryabikov, Valérie Tikhonoff, Katarzyna Stolarz, Giuseppe Bianchi, Edoardo Casiglia et al. · 2004 · Circulation
- Signal transducer of inflammation gp130 modulates atherosclerosis in mice and manLuchtefeld, Maren, Schunkert, Heribert, Stoll, Monika, Selle, Tina, Lorier, Rachel, Grote, Karsten, Sagebiel, Christian, Jagavelu, Kumaravelu, Tietge, Uwe J.F., Assmus, Ulrike et al. · 2007 · The Journal of Experimental Medicine
- Genome-wide linkage scan reveals multiple susceptibility loci influencing lipid and lipoprotein levels in the Québec Family StudyYohan Bossé, Yvon C. Chagnon, Jean‐Pierre Després, Treva Rice, D. C. Rao, Claude Bouchard, Louis Përusse, Marie‐Claude Vohl · 2004 · Journal of Lipid Research
- Genome-Wide Association Study on Resistance to Stalk Rot Diseases in Grain SorghumAdedayo Adeyanju, Christopher R. Little, Jianming Yu, Tesfaye Tesso · 2015 · G3 Genes Genomes Genetics
- Clinical features of psychotic disorders and polymorphisms in HT2A, DRD2, DRD4, SLC6A3 (DAT1), and BDNF: A family based association studyAyman H. Fanous, Michael Churton Neale, Richard E. Straub, Bradley Todd Webb, F. Anthony O’Neill, Dermot Walsh, Kenneth S. Kendler · 2003 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Within-sibship GWAS improve estimates of direct genetic effectsLaurence J Howe, Michel Guillaume Nivard, Tim Morris, Ailin Falkmo Hansen, Humaira Rasheed, Yoonsu Cho, Geetha Chittoor, Penelope A. Lind, Teemu Palviainen, Matthijs D. van der Zee et al. · 2021 · bioRxiv (Cold Spring Harbor Laboratory)
- Genome-wide association studies and the genetic dissection of complex traitsSebastiani, Paola, Timofeev, Nadia, Dworkis, Daniel A., Perls, Thomas T., Steinberg, Martin H. · 2009 · American Journal of Hematology
- Integrating Social Science and Genetics: News from the Political FrontP. Hatemi, Christopher T. Dawes, Amanda Frost-Keller, Jaime E. Settle, B. Verhulst · 2011 · Biodemography and Social Biology
- Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseasesYi‐Ju Li, William K. Scott, Ling Zhang, Ping‐I Lin, Sofia A. Oliveira, Tara J. Skelly, Maurali P. Doraiswamy, Kathleen Anne Welsh-Bohmer, Eden R. Martin, Jonathan L. Haines et al. · 2005 · Neurobiology of Aging
- Prospects for Association Mapping in Classical Inbred Mouse StrainsBret A. Payseur, Michael Place · 2007 · Genetics
- Supporting evidence for LRRTM1 imprinting effects in schizophreniaKerstin U. Ludwig, Manuel Mattheisen, T. W. Mühleisen, Darina Roeske, Christine Schmäl, René Breuer, Gerd Schulte‐Körne, Bertram Müller‐Myhsok, Markus Maria Nöthen, Per Hoffmann et al. · 2009 · Molecular Psychiatry
- Genetic influence on thrombotic risk markers in the elderly – a Danish twin studyElse‐Marie Bladbjerg, Moniek P.M. de Maat, Kaare Christensen, Lise Bathum, Jørgen Jespersen, Jacob Hjelmborg · 2005 · Journal of Thrombosis and Haemostasis
- A regulatory SNP of the BICD1 gene contributes to telomere length variation in humansMassimo Mangino, Scott Brouilette, Peter S. Braund, Nighat Tirmizi, Mariuca Vasa‐Nicotera, John Russell Thompson, Nilesh J. Samani · 2008 · Human Molecular Genetics
- SNPs in Dopamine D2 Receptor Gene (DRD2) and Norepinephrine Transporter Gene (NET) Are Associated with Continuous Performance Task (CPT) Phenotypes in ADHD children and their familiesS. Kollins, A. Anastopoulos, AM Lachiewicz, D. Fitzgerald, E. Morrissey-Kane, M. Garrett, SL Keatts, AE Ashley-Koch · 2008 · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
- Interaction between a novel TGFB1 haplotype and CFTR genotype is associated with improved lung function in cystic fibrosisLindsay A. Bremer, Scott M. Blackman, Lori L. Vanscoy, Kathryn E. McDougal, Amanda Bowers, Kathleen Naughton, David J. Cutler, Garry R. Cutting · 2008 · Human Molecular Genetics
- Functional genetic screen of human diversity reveals that a methionine salvage enzyme regulates inflammatory cell deathDennis C. Ko, Eric R. Gamazon, Kajal P. Shukla, Richard A. Pfuetzner, Dale Whittington, Tarah D. Holden, M. Brittnacher, Christine T. Fong, Matthew C. Radey, Cassandra Ogohara et al. · 2012 · Proceedings of the National Academy of Sciences
- European lactase persistence genotype shows evidence of association with increase in body mass indexJohannes Kettunen, Kaisa Silander, Olli Saarela, Najaf Amin, Martina Müller‐Nurasyid, Nicholas John Timpson, Ida L. Surakka, Samuli Ripatti, Jaana H. Laitinen, Anna‐Liisa Hartikainen et al. · 2009 · Human Molecular Genetics
- 24-h ambulatory blood pressure is linked to chromosome 18q21–22 and genetic variation of NEDD4L associates with cross-sectional and longitudinal blood pressure in SwedesCristiano Fava, Fredrik von Wowern, Göran Berglund, J. Carlson, Bo Hedblad, Lena Rosberg, Philippe Burri, Peter Almgren, Olle Melander · 2006 · Kidney International
- Replication of Association Between Working Memory and Reelin, a Potential Modifier Gene in SchizophreniaJuho Wedenoja, Annamari Tuulio‐Henriksson, Jaana Suvisaari, Anu Loukola, Tiina Paunio, Timo Partonen, Teppo Varilo, Jouko K Lönnqvist, Leena Peltonen · 2009 · Biological Psychiatry
- Software engineering the mixed model for genome-wide association studies on large samplesZhiwu Zhang, Edward S. Buckler, Terry M. Casstevens, Peter J. Bradbury · 2009 · Briefings in Bioinformatics
- In vivo and in vitro genetic evidence of involvement of neuregulin 1 in immune system dysregulationKetan K. Marballi, Marlon P. Quinones, Fabio Jiménez, Michael Escamilla, Henriette Raventós, Maria Clara Soto‐Bernardini, Seema S. Ahuja, Consuelo Walss‐Bass · 2010 · Journal of Molecular Medicine
- Exploring Positional Candidate Genes: Linkage Conditional on Measured GenotypeLaura A. Almasy, John Blangero · 2004 · Behavior Genetics
- Genomewide linkage scan reveals novel loci modifying age of onset of Huntington's disease in the Venezuelan HD kindredsJavier Gayán, Denise Brocklebank, J. Michael Andresen, Gorka Alkorta‐Aranburu, M. Zameel Cader, Simone A. Roberts, Stacey Shawn Cherny, Nancy Sabin Wexler, Lon R. Cardon, David E. Housman · 2008 · Genetic Epidemiology
- Linkage and association between Plasmodium falciparum blood infection levels and chromosome 5q31–q33Laurence Flori, Brice Kumulungui, Christophe Aucan, C Esnault, Alfred Sababenedyo Traore, Francis Fumoux, Pascal Rihet · 2003 · Genes and Immunity
- Genetic variants associated with carboplatin-induced cytotoxicity in cell lines derived from AfricansR. Stephanie Huang, Shiwei Duan, Emily O. Kistner, Christine Mary Hartford, M. Eileen Dolan · 2008 · Molecular Cancer Therapeutics
- Vitamin D receptor gene polymorphisms are linked to and associated with adult heightD. H. Xiong, Fu‐Hua Xu, P. Y. Liu, Hui Shen, J-R Long, Leo Elze, Robert R. Recker, H-W Deng · 2005 · Journal of Medical Genetics
- Psychopathology in the Postgenomic EraRobert J. Plomin, Peter McGuffin · 2002 · Annual Review of Psychology
- Linkage and Allelic Association of Chromosome 5 Cytokine Cluster Genetic Markers with Atopy and Asthma Associated TraitsAndrew John Walley, Steven Wiltshire, Clare Ellis, William Cookson · 2001 · Genomics
- A transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parentsDerek Gordon, Chad A. Haynes, Christopher Johnnidis, Shailendra B. Patel, Anne M. Bowcock, Jürg Ott · 2004 · European Journal of Human Genetics
- Platinum Sensitivity–Related Germline Polymorphism Discovered via a Cell-Based Approach and Analysis of Its Association with Outcome in Ovarian Cancer PatientsR. Stephanie Huang, Sharon E. Johnatty, Eric R. Gamazon, Hae Kyung Im, Dana M. Ziliak, Shiwei Duan, Wei Zhang, Emily O. Kistner, Peixian Chen, Jonathan Beesley et al. · 2011 · Clinical Cancer Research
- Autosomal Linkage Analysis for the Level of Response to AlcoholMarc Alan Schuckit, Kirk C. Wilhelmsen, Tom L. Smith, Heidi S. Feiler, Penelope A. Lind, Leslie A. Lange, Jelger A. Kalmijn · 2005 · Alcoholism Clinical and Experimental Research
- INSIG-2 promoter polymorphism and obesity related phenotypes: association study in 1428 members of 248 familiesDarroch H. Hall, Thahira Rahman, Peter J Avery, Bernard D. Keavney · 2006 · BMC Medical Genetics
- Association Study of Parkin Gene Polymorphisms With Idiopathic Parkinson DiseaseSofia A. Oliveira, William K. Scott, MARTHA A. NANCE, Ray L. Watts, Jean Pintar Hubble, William C. Koller, Kelly E. Lyons, Rajesh Pahwa, Matthew B. Stern, Bradley C. Hiner et al. · 2003 · Archives of Neurology