Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases. || Public Health Genomics Knowledge Base (v1.2)

Public Health Genomics Knowledge Base (v1.2)

From CDC-Authored Genomics Publication Database

This database contains CDC-authored publications in public health genomics including infectious diseases, newborn screening, reproductive health, genetic testing, cancer, chronic diseases, birth defects and developmental disabilities, environmental and occupational health as well as laboratory, bioinformatics and statistical methods.

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• Down syndrome: national conference on patient registries, research databases, and biobanks.
  Oster-Granite Mary Lou et al. Mol. Genet. Metab. 104(1-2) 13-22

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From Guideline Database

This database contains updated guidelines, policies and recommendations on genomic research and practice, as provided by professional organizations, federal advisory groups, expert panels and policy groups.

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• Merging Electronic Health Record Data and Genomics for Cardiovascular Research: A Science Advisory From the American Heart Association.
  Published 2016 (American Heart Association)

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From HuGE Literature Finder Database

This database contains published literature on genetic associations and other human genome epidemiology

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• Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases.
  Human reproduction (Oxford, England) 2016 Jun .
  Tšuiko O, Nõukas M, Žilina O, Hensen K, Tapanainen J S, Mägi R, Kals M, Kivistik P A, Haller-Kikkatalo K, Salumets A, Kurg
• Tumor Organoids Fill the Niche.
  Cell stem cell 2016 Jun 18 (6): 686-7.
  Shroyer Noah
• Germline genetics of cancer of unknown primary (CUP) and its specific subtypes.
  Oncotarget 2016 Mar .
  Hemminki Kari, Chen Bowang, Kumar Abhishek, Melander Olle, Manjer Jonas, Hallmans Göran, Pettersson-Kymmer Ulrika, Ohlsson Claes, Folprecht Gunnar, Löffler Harald, Krämer Alwin, Försti As
• Population-specific genotype imputations using minimac or IMPUTE2.
  Nature protocols 2015 Sep 10 (9): 1285-96.
  van Leeuwen Elisabeth M, Kanterakis Alexandros, Deelen Patrick, Kattenberg Mathijs V, , Slagboom P Eline, de Bakker Paul I W, Wijmenga Cisca, Swertz Morris A, Boomsma Dorret I, van Duijn Cornelia M, Karssen Lennart C, Hottenga Jouke J
• Characterization of statin dose response in electronic medical records.
  Clinical pharmacology and therapeutics 2014 Mar 95 (3): 331-8.
  Wei W-Q, Feng Q, Jiang L, Waitara M S, Iwuchukwu O F, Roden D M, Jiang M, Xu H, Krauss R M, Rotter J I, Nickerson D A, Davis R L, Berg R L, Peissig P L, McCarty C A, Wilke R A, Denny J

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Public Health Genomics Knowledge Base (v1.2)