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Refinado por: Base de dados/Biblioteca: DOAJ Directory of Open Access Journals remover assunto: Genetic Aspects remover
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1
Validating a non-invasive, ALT-based non-alcoholic fatty liver phenotype in the million veteran program
Validating a non-invasive, ALT-based non-alcoholic fatty liver phenotype in the million veteran program
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Validating a non-invasive, ALT-based non-alcoholic fatty liver phenotype in the million veteran program

Serper, Marina ; Vujkovic, Marijana ; Kaplan, David E ; Carr, Rotonya M ; Lee, Kyung Min ; Shao, Qing ; Miller, Donald R ; Reaven, Peter D ; Phillips, Lawrence S ; O'Donnell, Christopher J ; Meigs, James B ; Wilson, Peter W F ; Vickers-Smith, Rachel ; Kranzler, Henry R ; Justice, Amy C ; Gaziano, John M ; Muralidhar, Sumitra ; Pyarajan, Saiju ; DuVall, Scott L ; Assimes, Themistocles L ; Lee, Jennifer S ; Tsao, Philip S ; Rader, Daniel J ; Damrauer, Scott M ; Lynch, Julie A ; Saleheen, Danish ; Voight, Benjamin F ; Chang, Kyong-Mi Palmer, Nicholette D.

PloS one, 2020-08, Vol.15 (8), p.e0237430-e0237430 [Periódico revisado por pares]

United States: Public Library of Science

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2
A Melanoma Brain Metastasis with a Donor-Patient Hybrid Genome following Bone Marrow Transplantation: First Evidence for Fusion in Human Cancer
A Melanoma Brain Metastasis with a Donor-Patient Hybrid Genome following Bone Marrow Transplantation: First Evidence for Fusion in Human Cancer
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A Melanoma Brain Metastasis with a Donor-Patient Hybrid Genome following Bone Marrow Transplantation: First Evidence for Fusion in Human Cancer

Lazova, Rossitza ; Laberge, Greggory S ; Duvall, Eric ; Spoelstra, Nicole ; Klump, Vincent ; Sznol, Mario ; Cooper, Dennis ; Spritz, Richard A ; Chang, Joseph T ; Pawelek, John M Mezey, Eva

PloS one, 2013-06, Vol.8 (6), p.e66731-e66731 [Periódico revisado por pares]

United States: Public Library of Science

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3
Identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networks
Identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networks
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Identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networks

Kim, Minsu ; Huffman, Jennifer E ; Justice, Amy ; Goethert, Ian ; Agasthya, Greeshma ; Danciu, Ioana

BMC medical genomics, 2022-07, Vol.15 (1), p.151-151, Article 151 [Periódico revisado por pares]

England: BioMed Central Ltd

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4
Variability among the Isolates of Broad Bean Mottle Virus and Encapsidation of Host RNAs
Variability among the Isolates of Broad Bean Mottle Virus and Encapsidation of Host RNAs
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Variability among the Isolates of Broad Bean Mottle Virus and Encapsidation of Host RNAs

Shrestha, Nipin ; Duvall, Melvin R ; Bujarski, Jozef J

Pathogens (Basel), 2022-07, Vol.11 (7), p.817 [Periódico revisado por pares]

Basel: MDPI AG

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5
Phenome-wide association of 1809 phenotypes and COVID-19 disease progression in the Veterans Health Administration Million Veteran Program
Phenome-wide association of 1809 phenotypes and COVID-19 disease progression in the Veterans Health Administration Million Veteran Program
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Phenome-wide association of 1809 phenotypes and COVID-19 disease progression in the Veterans Health Administration Million Veteran Program

Song, Rebecca J ; Ho, Yuk-Lam ; Schubert, Petra ; Park, Yojin ; Posner, Daniel ; Lord, Emily M ; Costa, Lauren ; Gerlovin, Hanna ; Kurgansky, Katherine E ; Anglin-Foote, Tori ; DuVall, Scott ; Huffman, Jennifer E ; Pyarajan, Saiju ; Beckham, Jean C ; Chang, Kyong-Mi ; Liao, Katherine P ; Djousse, Luc ; Gagnon, David R ; Whitbourne, Stacey B ; Ramoni, Rachel ; Muralidhar, Sumitra ; Tsao, Philip S ; O'Donnell, Christopher J ; Gaziano, John Michael ; Casas, Juan P ; Cho, Kelly Marconi, Vincent C.

PloS one, 2021-05, Vol.16 (5), p.e0251651-e0251651 [Periódico revisado por pares]

United States: Public Library of Science

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6
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
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Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

Bucan, Maja ; Abrahams, Brett S ; Wang, Kai ; Glessner, Joseph T ; Herman, Edward I ; Sonnenblick, Lisa I ; Alvarez Retuerto, Ana I ; Imielinski, Marcin ; Hadley, Dexter ; Bradfield, Jonathan P ; Kim, Cecilia ; Gidaya, Nicole B ; Lindquist, Ingrid ; Hutman, Ted ; Sigman, Marian ; Kustanovich, Vlad ; Lajonchere, Clara M ; Singleton, Andrew ; Kim, Junhyong ; Wassink, Thomas H ; McMahon, William M ; Owley, Thomas ; Sweeney, John A ; Coon, Hilary ; Nurnberger, John I ; Li, Mingyao ; Cantor, Rita M ; Minshew, Nancy J ; Sutcliffe, James S ; Cook, Edwin H ; Dawson, Geraldine ; Buxbaum, Joseph D ; Grant, Struan F A ; Schellenberg, Gerard D ; Geschwind, Daniel H ; Hakonarson, Hakon Gibson, Greg

PLoS genetics, 2009-06, Vol.5 (6), p.e1000536 [Periódico revisado por pares]

United States: Public Library of Science

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7
Defining the contribution of CNTNAP2 to autism susceptibility
Defining the contribution of CNTNAP2 to autism susceptibility
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Defining the contribution of CNTNAP2 to autism susceptibility

Sampath, Srirangan ; Bhat, Shambu ; Gupta, Simone ; O'Connor, Ashley ; West, Andrew B ; Arking, Dan E ; Chakravarti, Aravinda Devaney, Joseph

PloS one, 2013-10, Vol.8 (10), p.e77906-e77906 [Periódico revisado por pares]

United States: Public Library of Science

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8
Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs
Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs
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Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs

Fradin, Delphine ; Cheslack-Postava, Keely ; Ladd-Acosta, Christine ; Newschaffer, Craig ; Chakravarti, Aravinda ; Arking, Dan E ; Feinberg, Andrew ; Fallin, M Daniele Dubé, Marie-Pierre

PloS one, 2010-09, Vol.5 (9), p.e12513 [Periódico revisado por pares]

United States: Public Library of Science

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9
A Novel Stratification Method in Linkage Studies to Address Inter- and Intra-Family Heterogeneity in Autism
A Novel Stratification Method in Linkage Studies to Address Inter- and Intra-Family Heterogeneity in Autism
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A Novel Stratification Method in Linkage Studies to Address Inter- and Intra-Family Heterogeneity in Autism

Talebizadeh, Zohreh ; Arking, Dan E ; Hu, Valerie W Mittal, Balraj

PloS one, 2013-06, Vol.8 (6), p.e67569-e67569 [Periódico revisado por pares]

United States: Public Library of Science

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10
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
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Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes

Pettigrew, Kerry A ; Frinton, Emily ; Nudel, Ron ; Chan, May T M ; Thompson, Paul ; Hayiou-Thomas, Marianna E ; Talcott, Joel B ; Stein, John ; Monaco, Anthony P ; Hulme, Charles ; Snowling, Margaret J ; Newbury, Dianne F ; Paracchini, Silvia

Journal of neurodevelopmental disorders, 2016-06, Vol.8 (1), p.24-24, Article 24 [Periódico revisado por pares]

England: BioMed Central Ltd

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