cran: GMMAT | Projects | Ecosyste.ms: Papers

10.3389/fgene.2021.682638

Scalable and Robust Regression Methods for Phenome-Wide Association Analysis on Large-Scale Biobank Data
Cited by: 2
Author(s): Wenjian Bi, Seunggeun Lee
Software Mentions: 10
Published: over 3 years ago

10.1371/journal.pgen.1009772

Rare variants in the endocytic pathway are associated with Alzheimer’s disease, its related phenotypes, and functional consequences
Cited by: 0
Author(s): Lingyu Zhan, Jiajin Li, Brandon Jew, Jae Hoon Sul
Software Mentions: 7
Published: over 3 years ago

10.1186/s12859-020-03862-2

Mixed logistic regression in genome-wide association studies
Cited by: 2
Author(s): Jacqueline Milet, David Courtin, André Garcia, Hervé Perdry
Software Mentions: 5
Published: about 4 years ago

10.3389/fgene.2020.00573

Phenotypic Responses to and Genetic Architecture of Sterility Following Exposure to Sub-Lethal Temperature During Development
Cited by: 21
Author(s): Martyna K. Zwoinska, Leonor R. Rodrigues, Jon Slate, Rhonda R. Snook
Software Mentions: 4
Published: over 4 years ago

10.1038/s41598-021-82547-z

An evaluation of approaches for rare variant association analyses of binary traits in related samples
Cited by: 4
Author(s): Ming-Huei Chen, Achilleas Pitsillides, Qiong Yang
Software Mentions: 4
Published: almost 4 years ago

10.1038/s41380-019-0558-2

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders
Cited by: 29
Author(s): Till F. M. Andlauer, José Guzmán-Parra, Fabian Streit, Jana Strohmaier, Maria J. Gonzalez, Susana Gil Flores, Francisco J. Cabaleiro Fabeiro, Francisco del Río Noriega, Fermín Pérez, Jesus Haro González, Guillermo Orozco Díaz, Yolanda de Diego-Otero, Berta Moreno‐Küstner, Georg Auburger, Franziska Degenhardt, Stefanie Heilmann‐Heimbach, Stefan Herms, Per Hoffmann, Josef Frank, Jerome C. Foo, Jens Treutlein, Stephanie H. Witt, Sven Cichon, Manolis Kogevinas, Fabio Rivas, Fermín Mayoral, Bertram Müller‐Myhsok, Andreas J. Forstner, Markus M. Nöthen, Marcella Rietschel
Software Mentions: 3
Published: about 5 years ago

10.1371/journal.pone.0236197

Family-based exome sequencing combined with linkage analyses identifies rare susceptibility variants of MUC4 for gastric cancer
Cited by: 3
Author(s): Young-Wook Choi, Jung Hun Ohn, Nayoung Kim, Wonji Kim, Kyungtaek Park, Sungho Won, Lee Sael, Cheol Min Shin, Sun Min Lee, Sejoon Lee, Hyun Joo An, Dong Man Jang, Byung Woo Han, Hye Seung Lee, Seung Joo Kang, Sang Woo Kim, Dong Hoon Lee
Software Mentions: 3
Published: over 4 years ago

10.1371/journal.pone.0253611

Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program
Cited by: 4
Author(s): Chloé Sarnowski, Han Chen, Mary L. Biggs, Sylvia Wassertheil‐Smoller, Jan Bressler, Marguerite R. Irvin, Kathleen A. Ryan, David Karasik, Donna K. Arnett, L. Adrienne Cupples, David W. Fardo, Stephanie M. Gogarten, Benjamin D. Heavner, Deepti Jain, Hyun Min Kang, Charles Kooperberg, Arch G. Mainous, Braxton D. Mitchell, Alanna C. Morrison, Jeffrey R. O’Connell, Bruce M. Psaty, Kenneth Rice, Albert V. Smith, Ramachandran S. Vasan, B. Gwen Windham, Douglas P. Kiel, Joanne M. Murabito, Kathryn L. Lunetta, TOPMed Longevity
Software Mentions: 3
Published: over 3 years ago

10.1186/s12863-018-0647-2

Application of novel and existing methods to identify genes with evidence of epigenetic association: results from GAW20
Cited by: 1
Author(s): Angga M Fuady, Samantha Lent, Chloé Sarnowski, Nathan L. Tintle
Software Mentions: 3
Published: over 6 years ago

10.1038/s41598-020-77209-5

Determinants of vitamin D status in Kenyan calves
Cited by: 3
Author(s): Rebecca Callaby, Emma Hurst, Ian Handel, Phil Toye, Barend Mark de Clare Bronsvoort, Richard J. Mellanby
Software Mentions: 3
Published: about 4 years ago

10.3390/genes12091368

The Genetic Architecture of a Congenital Heart Defect Is Related to Its Fitness Cost
Cited by: 1
Author(s): Ehiole Akhirome, Suk D. Regmi, Rachel A. Magnan, Nelson Ugwu, Yidan Qin, Claire E. Schulkey, James M. Cheverud, Patrick Y. Jay
Software Mentions: 2
Published: over 3 years ago

10.3390/ijerph14101134

An Efficient Test for Gene-Environment Interaction in Generalized Linear Mixed Models with Family Data
Cited by: 5
Author(s): Mauricio A. Mazo-Lopera, Brandon J. Coombes, Mariza de Andrade
Software Mentions: 2
Published: about 7 years ago

10.1186/s40246-019-0205-7

Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans
Cited by: 30
Author(s): Meijian Guan, Jacob M. Keaton, Latchezar Dimitrov, Pamela J. Hicks, Jianzhao Xu, Nicholette D. Palmer, Lijun Ma, Swapan K. Das, Yii‐Der I. Chen, Josef Coresh, Myriam Fornage, Nora Franceschini, Holly Kramer, Carl D. Langefeld, Josyf C. Mychaleckyj, Rulan S. Parekh, Wendy S. Post, Laura J. Rasmussen‐Torvik, Stephen S. Rich, Jerome I. Rotter, John R. Sedor, Denyse Thornley‐Brown, Adrienne Tin, James G. Wilson, Barry I. Freedman, Donald W. Bowden, Maggie Ng
Software Mentions: 2
Published: over 5 years ago

10.1038/s41398-020-01146-0

Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families
Cited by: 20
Author(s): José Guzmán-Parra, Fabian Streit, Andreas J. Forstner, Jana Strohmaier, Maria J. Gonzalez, Susana Gil Flores, Francisco J. Cabaleiro Fabeiro, Francisco del Río Noriega, Fermín Pérez, Jesus Haro González, Guillermo Orozco Díaz, Yolanda de Diego-Otero, Berta Moreno‐Küstner, Georg Auburger, Franziska Degenhardt, Stefanie Heilmann‐Heimbach, Stefan Herms, Per Hoffmann, Josef Frank, Jerome C. Foo, Lea Sirignano, Stephanie H. Witt, Sven Cichon, Fabio Rivas, Fermín Mayoral, Markus M. Nöthen, Till F. M. Andlauer, Marcella Rietschel
Software Mentions: 2
Published: almost 4 years ago

10.3389/fnins.2018.00592

Targeted Sequencing of Alzheimer Disease Genes in African Americans Implicates Novel Risk Variants
Cited by: 24
Author(s): Mark W. Logue, Daniel Lancour, John Farrell, Irina Simkina, M. Daniele Fallin, Kathryn L. Lunetta, Lindsay A. Farrer
Software Mentions: 1
Published: over 6 years ago

10.3390/genes12050736

Statistical Learning Methods Applicable to Genome-Wide Association Studies on Unbalanced Case-Control Disease Data
Cited by: 3
Author(s): Xiaotian Dai, Guifang Fu, Shaofei Zhao, Yifei Zeng
Software Mentions: 1
Published: over 3 years ago

10.1007/s00125-021-05461-z

Physical activity attenuates postprandial hyperglycaemia in homozygous TBC1D4 loss-of-function mutation carriers
Cited by: 5
Author(s): Theresia M. Schnurr, Emil Jørsboe, Alexandra Chadt, Inger Katrine Dahl-Petersen, Jonas M. Kristensen, Jørgen F. P. Wojtaszewski, Christian Springer, Peter Bjerregaard, Søren Brage, Oluf Pedersen, Ida Moltke, Niels Grarup, Hadi Al‐Hasani, Anders Albrechtsen, Marit Eika Jørgensen, Torben Hansen
Software Mentions: 1
Published: over 3 years ago

10.1038/s41598-018-35707-7

Associations between SLC16A11 variants and diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)
Cited by: 9
Author(s): Bertha Hidalgo, Tamar Sofer, Qibin Qi, Neil Schneiderman, Y. D.Ida Chen, Robert C. Kaplan, M. Larissa Avilés-Santa, Kari E. North, Donna K. Arnett, Adam A. Szpiro, Jianwen Cai, Bing Yu, Eric Boerwinkle, George Papanicolaou, Cathy C. Laurie, Jerome I. Rotter, Adrienne M. Stilp
Software Mentions: 1
Published: almost 6 years ago

10.1371/journal.pgen.1006329

CERAMIC: Case-Control Association Testing in Samples with Related Individuals, Based on Retrospective Mixed Model Analysis with Adjustment for Covariates
Cited by: 15
Author(s): Sheng Zhong, Duo Jiang, Mary Sara McPeek
Software Mentions: 1
Published: about 8 years ago

10.1038/s41398-020-0758-1

Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates
Cited by: 22
Author(s): Jae Hoon Sul, Alden Huang, Vasily Ramensky, Sun Hwang, Terri Teshiba, Young Jun Park, Anil P.S. Ori, Zhongyang Zhang, Niamh Mullins, Loes Olde Loohuis, Scott C. Fears, Carmen Araya, Xinia Araya, Mitzi Spesny, Julio Bejarano, Mark Ramirez, Gabriel Castrillón, Juliana Gomez-Makhinson, María Cecilia López, Gabriel Montoya, Claudia Patricia Montoya, Ileana Aldana, Javier I. Escobar, Jorge Ospina‐Duque, Bárbara Kremeyer, Gabriel Bedoya, Andrés Ruiz-Linares, Rita M. Cantor, Julio Molina, Giovanni Coppola, Roel A. Ophoff, Gabriel Macaya, Carlos López‐Jaramillo, Victor I. Reus, Carrie E. Bearden, Chiara Sabatti, Nelson B. Freimer
Software Mentions: 1
Published: almost 5 years ago

10.1371/journal.pone.0207752

An assessment of the performance of the logistic mixed model for analyzing binary traits in maize and sorghum diversity panels
Cited by: 10
Author(s): Esperanza M. Shenstone, Julian Cooper, Brian R. Rice, Martin Bohn, Tiffany M. Jamann, Alexander E. Lipka
Software Mentions: 1
Published: about 6 years ago

10.1371/journal.pone.0186331

XX Disorder of Sex Development is associated with an insertion on chromosome 9 and downregulation of RSPO1 in dogs (Canis lupus familiaris)
Cited by: 12
Author(s): Vicki N. Meyers-Wallen, Adam R. Boyko, Charles G. Danko, Jennifer K. Grenier, Jason G. Mezey, Jessica J. Hayward, Laura M. Shannon, Chuan Gao, Afrah Shafquat, Edward J. Rice, Shashikant Pujar, Stefanie Eggers, Thomas Ohnesorg, Andrew H. Sinclair
Software Mentions: 1
Published: about 7 years ago

10.1038/s41435-019-0082-z

Elevated risk of invasive group A streptococcal disease and host genetic variation in the human leucocyte antigen locus
Cited by: 4
Author(s): Tom Parks, Katherine S. Elliott, Theresa Lamagni, Kathryn Auckland, Alexander J. Mentzer, Rebecca Guy, Doreen Cartledge, Lenka Straková, Daniel O’Connor, Andrew J. Pollard, Matthew J. Neville, Anubha Mahajan, Houman Ashrafian, S. Jonathan Chapman, Hill Avs., Shiranee Sriskandan, Julian C. Knight
Software Mentions: 1
Published: over 5 years ago

10.1038/s41431-021-00838-5

Identification of novel locus associated with coronary artery aneurysms and validation of loci for susceptibility to Kawasaki disease
Cited by: 8
Author(s): Clive Hoggart, Chisato Shimizu, Rachel Galassini, Victoria J. Wright, Hannah Shailes, Evangelos Bellos, Jethro Herberg, Andrew J. Pollard, Daniel O’Connor, Shing Wan Choi, Eleanor G. Seaby, Stephanie Menikou, Martin L. Hibberd, Neneh Sallah, David Burgner, Paul Brogan, Harsita Patel, Jihoon Kim, Adriana H. Tremoulet, Eeva Salo, Diana van Stijn, Taco W. Kuijpers, Jane C. Burns, Michael Levin
Software Mentions: 1
Published: almost 4 years ago

10.3389/fgene.2017.00049

A Pragmatic Test for Detecting Association between a Dichotomous Trait and the Genotypes of Affected Families, Controls and Independent Cases
Cited by: 2
Author(s): Meng Wang, William C. Stewart
Software Mentions: 1
Published: over 7 years ago

10.1186/s12917-020-02344-0

Identification of single-nucleotide variants associated with susceptibility to Salmonella in pigs using a genome-wide association approach
Cited by: 4
Author(s): Corinne H. Schut, Abdolvahab Farzan, Russell S. Fraser, Margaret H Ainslie-Garcia, Robert Friendship, Brandon N. Lillie
Software Mentions: 1
Published: over 4 years ago

Ecosyste.ms: Papers

Projects: cran: GMMAT

Papers Mentioning GMMAT 26