Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Brandi L. Kattman"'
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 9, Iss 8, Pp 2447-2461 (2019)
Inferring subject ancestry using genetic data is an important step in genetic association studies, required for dealing with population stratification. It has become more challenging to infer subject ancestry quickly and accurately since large amount
Externí odkaz:
https://doaj.org/article/cb84436f63564bf5b4a52051c1c0575d
Autor:
Rama Maiti, Chao Chen, Douglas W. Hoffman, J. Bradley Holmes, Donna Maglott, Joseph Mitchell, Baoshan Gu, Garth Brown, Melissa J. Landrum, Brandi L. Kattman, Vitaly Lyoshin, Kuljeet Kaur, George Zhou, George R. Riley, Wonhee Jang, Jennifer Hart, Nuala A. O'Leary, Chunlei Liu, Valerie A. Schneider, Shanmuga Chitipiralla, Wenyao Shi, Zenith Maddipatla
Publikováno v:
Nucleic Acids Research. 48:D835-D844
ClinVar is a freely available, public archive of human genetic variants and interpretations of their relationships to diseases and other conditions, maintained at the National Institutes of Health (NIH). Submitted interpretations of variants are aggr
Publikováno v:
Bioinformatics
MotivationNormalizing diverse representations of sequence variants is critical to the elucidation of the genetic basis of disease and biological function. NCBI has long wrestled with integrating data from multiple submitters to build databases such a
Publikováno v:
G3: Genes|Genomes|Genetics
G3: Genes, Genomes, Genetics, Vol 9, Iss 8, Pp 2447-2461 (2019)
G3: Genes, Genomes, Genetics, Vol 9, Iss 8, Pp 2447-2461 (2019)
Inferring subject ancestry using genetic data is an important step in genetic association studies, required for dealing with population stratification. It has become more challenging to infer subject ancestry quickly and accurately since large amount
Publikováno v:
Molecular Genetics and Metabolism. 132:S341-S342
Autor:
Jennifer M. Lee, George R. Riley, Chen Chao, Kurt McDaniel, Brandi L. Kattman, Donna Maglott, Zenith Maddipatla, Melissa J. Landrum, Baoshan Gu, Douglas W. Hoffman, Kenneth S. Katz, Garth Brown, J. Bradley Holmes, Mark L. Benson, George Zhou, Karen Karapetyan, Chunlei Liu, Shanmuga Chitipiralla, Michael Ovetsky, Malheiro Aj, Wonhee Jang, Jennifer Hart
Publikováno v:
Nucleic Acids Research
ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, public archive of human genetic variants and interpretations of their significance to disease, maintained at the National Institutes of Health. Interpretations of the clinical sig
Autor:
Wonhee Jang, Melissa J. Landrum, Kuljeet Kaur, Vitaly Lyoshin, Andrew Russette, Chao Chen, Zenith Maddipatla, Baoshan Gu, Shanmuga Chitipiralla, Joseph Mitchell, Brandi L. Kattman, Douglas W. Hoffman
Publikováno v:
Molecular Genetics and Metabolism. 132:S150
Autor:
Juliann M. Savatt, Brandi L. Kattman, David H. Ledbetter, Melissa J. Landrum, Christa Lese Martin, W. Andrew Faucett, Jo Anne Vidal, Heidi L. Rehm, Jennifer Hart, Jud Rhode, Stefanie Turner, Emily Palen, Karen E. Wain, Vanessa Rangel Miller, Danielle R. Azzariti, Steven M. Harrison, Erin Rooney Riggs
GenomeConnect, the NIH-funded Clinical Genome Resource (ClinGen) patient registry, engages patients in data sharing to support the goal of creating a genomic knowledge base to inform clinical care and research. Participant self-reported health inform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::445be7de51d7da29ef235a6025c28d4a
https://europepmc.org/articles/PMC6188701/
https://europepmc.org/articles/PMC6188701/
Autor:
Douglas W. Hoffman, Marilu A. Hoeppner, Zenith Maddipatla, Malheiro Aj, Donna Maglott, Wonhee Jang, Chunlei Liu, Joe Mitchell, Baoshan Gu, Shanmuga Chitipiralla, Brandi L. Kattman, George Zhou, Dean Lc, Wenyao Shi, Chao Chen, Vitaliy Lyoshin
Publikováno v:
Journal of Clinical Oncology. 38:e14141-e14141
e14141 Background: Oncology is one of the few medical specialties where pharmacogenetic dosing is becoming a routine part of patient management. In the US, oncology drugs account for one-third of all drugs with pharmacogenetic data in their labeling.
Publikováno v:
Journal of Clinical Oncology. 37:e22000-e22000
e22000 Background: Oncology professionals need to access a wide range of genetic tests, including tests for cancer biomarkers, predisposition to hereditary cancers, and pharmacogenetic tests. While pharmacogenetic testing is fundamental to personaliz