Works matching IS 09646906 AND DT 2020 AND VI 29 AND IP R1

Results: 15

Implicit bias of encoded variables: frameworks for addressing structured bias in EHR–GWAS data.

Published in:

Human Molecular Genetics, 2020, v. 29, n. R1, p. R33, doi. 10.1093/hmg/ddaa192

By:

Dueñas, Hillary R;
Seah, Carina;
Johnson, Jessica S;
Huckins, Laura M

Publication type:

Article

Genetic risk factors of ME/CFS: a critical review.

Published in:

Human Molecular Genetics, 2020, v. 29, n. R1, p. R117, doi. 10.1093/hmg/ddaa169

By:

Dibble, Joshua J;
McGrath, Simon J;
Ponting, Chris P

Publication type:

Article

Genetics of early growth traits.

Published in:

Human Molecular Genetics, 2020, v. 29, n. R1, p. R66, doi. 10.1093/hmg/ddaa149

By:

Cousminer, Diana L;
Freathy, Rachel M

Publication type:

Article

Fine-mapping genetic associations.

Published in:

Human Molecular Genetics, 2020, v. 29, n. R1, p. R81, doi. 10.1093/hmg/ddaa148

By:

Hutchinson, Anna;
Asimit, Jennifer;
Wallace, Chris

Publication type:

Article

Functional annotation of genomic variation: DNA methylation episignatures in neurodevelopmental Mendelian disorders.

Published in:

Human Molecular Genetics, 2020, v. 29, n. R1, p. R27, doi. 10.1093/hmg/ddaa144

By:

Sadikovic, Bekim;
Levy, Michael A;
Aref-Eshghi, Erfan

Publication type:

Article

The phenomenal epigenome in neurodevelopmental disorders.

Published in:

Human Molecular Genetics, 2020, v. 29, n. R1, p. R42, doi. 10.1093/hmg/ddaa175

By:

Ciptasari, Ummi;
Bokhoven, Hans van

Publication type:

Article

Dissecting genome-wide studies for microbiome-related metabolic diseases.

Published in:

Human Molecular Genetics, 2020, v. 29, n. R1, p. R73, doi. 10.1093/hmg/ddaa105

By:

Awany, Denis;
Allali, Imane;
Chimusa, Emile R

Publication type:

Article

Regulation, diversity and function of MECP2 exon and 3′UTR isoforms.

Published in:

Human Molecular Genetics, 2020, v. 29, n. R1, p. R89, doi. 10.1093/hmg/ddaa154

By:

Rodrigues, Deivid Carvalho;
Mufteev, Marat;
Ellis, James

Publication type:

Article

Functional genomics in autoimmune diseases.

Published in:

Human Molecular Genetics, 2020, v. 29, n. R1, p. R59, doi. 10.1093/hmg/ddaa097

By:

Ding, James;
Frantzeskos, Antonios;
Orozco, Gisela

Publication type:

Article

Genomics at cellular resolution: insights into cognitive disorders and their evolution.

Published in:

Human Molecular Genetics, 2020, v. 29, n. R1, p. R1, doi. 10.1093/hmg/ddaa117

By:

Berto, Stefano;
Liu, Yuxiang;
Konopka, Genevieve

Publication type:

Article

Temple syndrome and Kagami-Ogata syndrome: clinical presentations, genotypes, models and mechanisms.

Published in:

Human Molecular Genetics, 2020, v. 29, n. R1, p. R107, doi. 10.1093/hmg/ddaa133

By:

Prasasya, Rexxi;
Grotheer, Kristen V;
Siracusa, Linda D;
Bartolomei, Marisa S

Publication type:

Article

Reviewing the genetics of heterogeneity in depression: operationalizations, manifestations and etiologies.

Published in:

Human Molecular Genetics, 2020, v. 29, n. R1, p. R10, doi. 10.1093/hmg/ddaa115

By:

Cai, Na;
Choi, Karmel W;
Fried, Eiko I

Publication type:

Article

Understanding human gut diseases at single-cell resolution.

Published in:

Human Molecular Genetics, 2020, v. 29, n. R1, p. R51, doi. 10.1093/hmg/ddaa130

By:

Bigaeva, Emilia;
Venema, Werna T C Uniken;
Weersma, Rinse K;
Festen, Eleonora A M

Publication type:

Article

Genome editing strategies for fetal hemoglobin induction in beta-hemoglobinopathies.

Published in:

Human Molecular Genetics, 2020, v. 29, n. R1, p. R100, doi. 10.1093/hmg/ddaa088

By:

Demirci, Selami;
Leonard, Alexis;
Tisdale, John F

Publication type:

Article

Androgen receptor variants: RNA-based mechanisms and therapeutic targets.

Published in:

Human Molecular Genetics, 2020, v. 29, n. R1, p. R19, doi. 10.1093/hmg/ddaa089

By:

Tietz, Kiel T;
Dehm, Scott M

Publication type:

Article