Erin M Ramos

Erin M Ramos

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Erin M Ramos

Erin M Ramos

Publications by authors named "Erin M Ramos"

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Points to consider for sharing variant-level information from clinical genetic testing with ClinVar.

Cold Spring Harb Mol Case Stud 2018 02 1;4(1). Epub 2018 Feb 1.

Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine, Cambridge, Massachusetts 02139, USA.

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http://dx.doi.org/10.1101/mcs.a002345DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793773PMC
February 2018

The dbGaP data browser: a new tool for browsing dbGaP controlled-access genomic data.

Nucleic Acids Res 2017 01 29;45(D1):D819-D826. Epub 2016 Nov 29.

National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20894, USA

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http://dx.doi.org/10.1093/nar/gkw1139DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210596PMC
January 2017

Using ClinVar as a Resource to Support Variant Interpretation.

Curr Protoc Hum Genet 2016 Apr 1;89:8.16.1-8.16.23. Epub 2016 Apr 1.

Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine, Cambridge, Massachusetts.

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http://dx.doi.org/10.1002/0471142905.hg0816s89DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832236PMC
April 2016

Using the PhenX Toolkit to Add Standard Measures to a Study.

Curr Protoc Hum Genet 2015 Jul 1;86:1.21.1-17. Epub 2015 Jul 1.

RTI International, Research Triangle Park, North Carolina.

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http://dx.doi.org/10.1002/0471142905.hg0121s86DOI Listing
July 2015

ClinGen--the Clinical Genome Resource.

N Engl J Med 2015 06 27;372(23):2235-42. Epub 2015 May 27.

From Harvard Medical School and Brigham and Women's Hospital and Partners HealthCare - all in Boston (H.L.R.); University of North Carolina, Chapel Hill (J.S.B., J.P.E.); National Human Genome Research Institute, National Institutes of Health (NIH) (L.D.B., E.M.R.), National Center for Biotechnology Information, National Library of Medicine, NIH (M.J.L., D.R.M., S.T.S.), and American College of Medical Genetics and Genomics (M.S.W.) - all in Bethesda, MD; Stanford University School of Medicine, Stanford (C.D.B.), and University of California, San Francisco, San Francisco (R.L.N.) - both in California; Geisinger Health System, Danville, PA (D.H.L., C.L.M.); and Baylor College of Medicine, Houston (S.E.P.).

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http://dx.doi.org/10.1056/NEJMsr1406261DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4474187PMC
June 2015

Phenotype-Genotype Integrator (PheGenI): synthesizing genome-wide association study (GWAS) data with existing genomic resources.

Eur J Hum Genet 2014 Jan 22;22(1):144-7. Epub 2013 May 22.

Division of Genomic Medicine, National Human Genome Research Institute, NIH, Bethesda, MD, USA.

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http://dx.doi.org/10.1038/ejhg.2013.96DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3865418PMC
January 2014

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers.

Authors:
Sarah M Hartz Susan E Short Nancy L Saccone Robert Culverhouse LiShiun Chen Tae-Hwi Schwantes-An Hilary Coon Younghun Han Sarah H Stephens Juzhong Sun Xiangning Chen Francesca Ducci Nicole Dueker Nora Franceschini Josef Frank Frank Geller Daniel Gubjartsson Nadia N Hansel Chenhui Jiang Kaisu Keskitalo-Vuokko Zhen Liu Leo-Pekka Lyytikäinen Martha Michel Rajesh Rawal Albert Rosenberger Paul Scheet John R Shaffer Alexander Teumer John R Thompson Jacqueline M Vink Nicole Vogelzangs Angela S Wenzlaff William Wheeler Xiangjun Xiao Bao-Zhu Yang Steven H Aggen Anthony J Balmforth Sebastian E Baumeister Terri Beaty Siiri Bennett Andrew W Bergen Heather A Boyd Ulla Broms Harry Campbell Nilanjan Chatterjee Jingchun Chen Yu-Ching Cheng Sven Cichon David Couper Francesco Cucca Danielle M Dick Tatiana Foroud Helena Furberg Ina Giegling Fangyi Gu Alistair S Hall Jenni Hällfors Shizhong Han Annette M Hartmann Caroline Hayward Kauko Heikkilä John K Hewitt Jouke Jan Hottenga Majken K Jensen Pekka Jousilahti Marika Kaakinen Steven J Kittner Bettina Konte Tellervo Korhonen Maria-Teresa Landi Tiina Laatikainen Mark Leppert Steven M Levy Rasika A Mathias Daniel W McNeil Sarah E Medland Grant W Montgomery Thomas Muley Tanda Murray Matthias Nauck Kari North Michele Pergadia Ozren Polasek Erin M Ramos Samuli Ripatti Angela Risch Ingo Ruczinski Igor Rudan Veikko Salomaa David Schlessinger Unnur Styrkársdóttir Antonio Terracciano Manuela Uda Gonneke Willemsen Xifeng Wu Goncalo Abecasis Kathleen Barnes Heike Bickeböller Eric Boerwinkle Dorret I Boomsma Neil Caporaso Jubao Duan Howard J Edenberg Clyde Francks Pablo V Gejman Joel Gelernter Hans Jörgen Grabe Hyman Hops Marjo-Riitta Jarvelin Jorma Viikari Mika Kähönen Kenneth S Kendler Terho Lehtimäki Douglas F Levinson Mary L Marazita Jonathan Marchini Mads Melbye Braxton D Mitchell Jeffrey C Murray Markus M Nöthen Brenda W Penninx Olli Raitakari Marcella Rietschel Dan Rujescu Nilesh J Samani Alan R Sanders Ann G Schwartz Sanjay Shete Jianxin Shi Margaret Spitz Kari Stefansson Gary E Swan Thorgeir Thorgeirsson Henry Völzke Qingyi Wei H-Erich Wichmann Christopher I Amos Naomi Breslau Dale S Cannon Marissa Ehringer Richard Grucza Dorothy Hatsukami Andrew Heath Eric O Johnson Jaakko Kaprio Pamela Madden Nicholas G Martin Victoria L Stevens Jerry A Stitzel Robert B Weiss Peter Kraft Laura J Bierut

Arch Gen Psychiatry 2012 Aug;69(8):854-60

Washington University School of Medicine, St Louis, Missouri, USA.

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http://dx.doi.org/10.1001/archgenpsychiatry.2012.124DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3482121PMC
August 2012

Using the PhenX Toolkit to Add Standard Measures to a Study.

Curr Protoc Hum Genet 2011 Oct;Chapter 1:Unit1.21

RTI International, Research Triangle Park, North Carolina, USA.

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http://dx.doi.org/10.1002/0471142905.hg0121s71DOI Listing
October 2011

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.

Proc Natl Acad Sci U S A 2009 Jun 27;106(23):9362-7. Epub 2009 May 27.

Office of Population Genomics, Genome Technology Branch, National Human Genome Research Institute, and National Center for Biotechnology Information, National Institutes of Health, Bethesda, MD 20892, USA.

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https://www.genome.gov/pages/about/od/newsandfeatures/pnasgw
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http://www.pnas.org/content/106/23/9362.full.pdf
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http://www.pnas.org/cgi/doi/10.1073/pnas.0903103106
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http://dx.doi.org/10.1073/pnas.0903103106DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2687147PMC
June 2009

Unravelling the contributions of social, environmental and genetic factors to health differences.

CMAJ 2008 Sep;179(7):629-30

Social and Behavioral Research Branch, Division of Intramural Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892-2070, USA.

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http://dx.doi.org/10.1503/cmaj.080669DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2535736PMC
September 2008

The National Alzheimer's Coordinating Center (NACC) database: the Uniform Data Set.

Alzheimer Dis Assoc Disord 2007 Jul-Sep;21(3):249-58

Department of Epidemiology, National Alzheimer's Coordinating Center, School of Public Health and Community Medicine, University of Washington, Seattle, WA 98105, USA.

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http://dx.doi.org/10.1097/WAD.0b013e318142774eDOI Listing
December 2007

Tumor necrosis factor alpha and interleukin 10 promoter region polymorphisms and risk of late-onset Alzheimer disease.

Arch Neurol 2006 Aug;63(8):1165-9

Institute for Public Health Genetics, Department of Medicine, University of Washington, Seattle, WA, USA.

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http://dx.doi.org/10.1001/archneur.63.8.1165DOI Listing
August 2006

The National Alzheimer's Coordinating Center (NACC) Database: an Alzheimer disease database.

Alzheimer Dis Assoc Disord 2004 Oct-Dec;18(4):270-7

National Alzheimer's Coordinating Center, Department of Epidemiology, School of Public Health and Community Medicine, University of Washington, Seattle, Washington 98105, USA.

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April 2005