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Results : 76-90/90

Improving Power in Contrasting Linkage-Disequilibrium Patterns between Cases and Controls

Authors: Wang, Tao Zhu, Xiaofeng Elston, Robert C.

Journal: American journal of human genetics

Citation: Wang, Tao et al., Improving Power in Contrasting Linkage-Disequilibrium Patterns between Cases and Controls, American journal of human genetics , 80(5), 2007, pp. 911-920

A Simple and Improved Correction for Population Stratification in Case-Control Studies

Authors: Epstein, Michael P. Allen, Andrew S. Satten, Glen A.

Journal: American journal of human genetics

Citation: P. Epstein, Michael et al., A Simple and Improved Correction for Population Stratification in Case-Control Studies, American journal of human genetics , 80(5), 2007, pp. 921-930

Phosphoserine Aminotransferase Deficiency: A Novel Disorder of the Serine Biosynthesis Pathway

Authors: Hart, Claire E. Race, Valerie Achouri, Younes Wiame, Elsa Sharrard, Mark Olpin, Simon E. Watkinson, Jennifer Bonham, James R. Jaeken, Jaak Matthijs, Gert Van Schaftingen, Emile

Journal: American journal of human genetics

Citation: E. Hart, Claire et al., Phosphoserine Aminotransferase Deficiency: A Novel Disorder of the Serine Biosynthesis Pathway, American journal of human genetics , 80(5), 2007, pp. 931-937

A Genomewide Single-Nucleotide.Polymorphism Panel for Mexican American Admixture Mapping

Authors: Tian, Chao Hinds, David A. Shigeta, Russell Adler, Sharon G. Lee, Annette Pahl, Madeleine V. Silva, Gabriel Belmont, John W. Hanson, Robert L. Knowler, William C. Gregersen, Peter K. Ballinger, Dennis G. Seldin, Michael F

Journal: American journal of human genetics

Citation: Tian, Chao et al., A Genomewide Single-Nucleotide.Polymorphism Panel for Mexican American Admixture Mapping, American journal of human genetics , 80(6), 2007, pp. 1014-1023

A Genomewide Admixture Map for Latino Populations

Authors: Price, Alkes L. Patterson, Nick Yu, Fuli Cox, David R. Waliszewska, Alicja McDonald, Gavin J. Tandon, Arti Schirmer, Christine Neubauer, Julie Bedoya, Gabriel Duque, Constanza Villegas, Alberto Bortolini, Maria Catira Salzano, Francisco M. Gallo, Carla Mazzotti, Guido Tello-Ruiz, Marcela Riba, Laura Aguilar-Salinas, Carlos A. Canizales-Quinteros, Samuel Reich, David

Journal: American journal of human genetics

Citation: L. Price, Alkes et al., A Genomewide Admixture Map for Latino Populations, American journal of human genetics , 80(6), 2007, pp. 1024-1036

Gene Copy-Number Variation and Associated Polymorphisms of Complement Component C4 in Human Systemic Lupus Erythematosus (SLE): Low Copy Number Is a Risk Factor for and High Copy Number Is a Protective Factor against SLE Susceptibility in European Americans

Authors: Yang, Yan Chung, Erwin K Wu, Yee Ling Savelli, Stephanie L. Nagaraja, Haikady N. Zhou, Bi Hebert, Maddie Jones, Karla N. Shu, Yaoling Kitzmiller, Kathryn Blanchong, Carol A. McBride, Kim L. Higgins, Gloria C. Rennebohm, Robert M. Rice, Robert R. Hackshaw, Kevin V. Roubey, Robert A.S. Grossman, Jennifer M. Tsao, Betty P. Birmingham, Daniel J. Yu, Chack Yung

Journal: American journal of human genetics

Citation: Yang, Yan et al., Gene Copy-Number Variation and Associated Polymorphisms of Complement Component C4 in Human Systemic Lupus Erythematosus (SLE): Low Copy Number Is a Risk Factor for and High Copy Number Is a Protective Factor against SLE Susceptibility in European Americans, American journal of human genetics , 80(6), 2007, pp. 1037-1054

Transcriptional Control of SLC26A4 Is Involved in Pendred Syndrome and Nonsyndromic Enlargement of Vestibular Aqueduct (DFNB4)

Authors: Yang, Tao Vidarsson, Hilmar Rodrigo-Blomqvist, Sandra Rosengren, Sally S. Enerbäck, Sven Smith, Richard J.H.

Journal: American journal of human genetics

Citation: Yang, Tao et al., Transcriptional Control of SLC26A4 Is Involved in Pendred Syndrome and Nonsyndromic Enlargement of Vestibular Aqueduct (DFNB4), American journal of human genetics , 80(6), 2007, pp. 1055-1063

Red-Green Color Vision Impairment in Duchenne Muscular Dystrophy

Authors: Costa, Marcelo Fernandes Fernandes Oliveira, Andre Gustavo Feitosa-Santana, Claudia Zatz, Mayana Fix Ventura, Dora

Journal: American journal of human genetics

Citation: Costa, Marcelo Fernandes et al., Red-Green Color Vision Impairment in Duchenne Muscular Dystrophy, American journal of human genetics , 80(6), 2007, pp. 1064-1075

A Mutation in CCDC50, a Gene Encoding an Effector of Epidermal Growth Factor.Mediated Cell Signaling, Causes Progressive Hearing Loss

Authors: Modamio-Høybjør, Silvia Mencía, Ángeles Goodyear, Richard Del Castillo, Ignacio Richardson, Guy Moreno, Felipe Moreno-Pelayo, Miguel Ángel

Journal: American journal of human genetics

Citation: Modamio-høybjør, Silvia et al., A Mutation in CCDC50, a Gene Encoding an Effector of Epidermal Growth Factor.Mediated Cell Signaling, Causes Progressive Hearing Loss, American journal of human genetics , 80(6), 2007, pp. 1076-1089

Homozygosity Haplotype Allows a Genomewide Search for the Autosomal Segments Shared among Patients

Authors: Miyazawa, Hitoshi Kato, Masaaki Awata, Takuya Kohda, Masakazu Iwasa, Hiroyasu Koyama, Nobuyuki Tanaka, Tomoaki",Huqun,"Kyo, Shunei Okazaki, Yasushi Hagiwara, Koichi

Journal: American journal of human genetics

Citation: Miyazawa, Hitoshi et al., Homozygosity Haplotype Allows a Genomewide Search for the Autosomal Segments Shared among Patients, American journal of human genetics , 80(6), 2007, pp. 1090-1102

IRAK-M Is Involved in the Pathogenesis of Early-Onset Persistent Asthma

Authors: Balaci, Lenuta Spada, Maria Cristina Olla, Nazario Sole, Gabriella Loddo, Laura Anedda, Francesca Naitza, Silvia Zuncheddu, Maria Antonietta Maschio, Andrea Altea, Daniele Uda, Manuela Pilia, Sabrina Sanna, Serena Marsala, Marco Crisponi, Laura Fattori, Matilde Devoto, Marcella Doratiotto, Silvia Rassu, Stefania Mereu, Simonetta Pilia, Giuseppe

Journal: American journal of human genetics

Citation: Balaci, Lenuta et al., IRAK-M Is Involved in the Pathogenesis of Early-Onset Persistent Asthma, American journal of human genetics , 80(6), 2007, pp. 1103-1114

A Common Haplotype in the G-Protein.Coupled Receptor Gene GPR74 Is Associated with Leanness and Increased Lipolysis

Authors: Dahlman, Ingrid Dicker, Andrea Jiao, Hong Kere, Juha Blomqvist, Lennart Van Harmelen, Vanessa Hoffstedt, Johan Borch-Johnsen, Knut Jörgensen, Torben Hansen, Torben Pedersen, Oluf Laakso, Markku Arner, Peter

Journal: American journal of human genetics

Citation: Dahlman, Ingrid et al., A Common Haplotype in the G-Protein.Coupled Receptor Gene GPR74 Is Associated with Leanness and Increased Lipolysis, American journal of human genetics , 80(6), 2007, pp. 1115-1124

A Generalized Combinatorial Approach for Detecting Gene-by-Gene and Gene-by-Environment Interactions with Application to Nicotine Dependence

Authors: Lou, Xiang-Yang Chen, Guo-Bo Yan, Lei Ma, Jennie Z. Zhu, Jun Elston, Robert C. Li, Ming D.

Journal: American journal of human genetics

Citation: Lou, Xiang-yang et al., A Generalized Combinatorial Approach for Detecting Gene-by-Gene and Gene-by-Environment Interactions with Application to Nicotine Dependence, American journal of human genetics , 80(6), 2007, pp. 1125-1137

Defining the Cause of Skewed X-Chromosome Inactivation in X-Linked Mental Retardation by Use of a Mouse Model

Authors: Muers, Mary R. Sharpe, Jacqueline A. Garrick, David Sloane-Stanley, Jacqueline Nolan, Patrick M. Hacker, Terry Wood, William G Higgs, Douglas R. Gibbons, Richard J.

Journal: American journal of human genetics

Citation: R. Muers, Mary et al., Defining the Cause of Skewed X-Chromosome Inactivation in X-Linked Mental Retardation by Use of a Mouse Model, American journal of human genetics , 80(6), 2007, pp. 1138-1149

Type 2 Diabetes TCF7L2 Risk Genotypes Alter Birth Weight: A Study of 24,053 Individuals

Authors: Freathy, Rachel M. Weedon, Michael N. Bennett, Amanda Hyppönen, Elina Relton,Caroline L. Knight, Beatrice Shields, Beverley Parnell, Kirstie S. Groves, Christopher J. Ring, Susan M Pembrey, Marcus E. Ben-Shlomo, Yoav Strachan, David P. Power, Chris Jarvelin, Marjo-Riitta McCarthy, Mark I. Smith, George Davey Hattersley, Andrew T. Frayling, Timothy M.

Journal: American journal of human genetics

Citation: M. Freathy, Rachel et al., Type 2 Diabetes TCF7L2 Risk Genotypes Alter Birth Weight: A Study of 24,053 Individuals, American journal of human genetics , 80(6), 2007, pp. 1150-1161

Results: 1-25 | 26-50 | 51-75 | 76-90