Nathan Pankratz

Nathan Pankratz

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Nathan Pankratz

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RE: "RACIAL AND ETHNIC DIFFERENCES IN SOCIOECONOMIC POSITION AND RISK OF CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA".

Am J Epidemiol 2019 Jun;188(6):1192-1193

Department of Pediatrics, Baylor College of Medicine, Houston, Texas.

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http://dx.doi.org/10.1093/aje/kwz075DOI Listing
June 2019

Large Genomic Aberrations in Corticotropinomas Are Associated With Greater Aggressiveness.

J Clin Endocrinol Metab 2019 May;104(5):1792-1801

Section on Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.

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http://dx.doi.org/10.1210/jc.2018-02164DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452317PMC
May 2019

Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels.

Circulation 2019 Jan;139(5):620-635

Department of Epidemiology, (A.P.R., B.M.P., N.L.S.), University of Washington, Seattle.

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http://dx.doi.org/10.1161/CIRCULATIONAHA.118.034532DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438386PMC
January 2019

Klinefelter syndrome in males with germ cell tumors: A report from the Children's Oncology Group.

Cancer 2018 Oct 6;124(19):3900-3908. Epub 2018 Oct 6.

Division of Epidemiology and Clinical Research, Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota.

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http://dx.doi.org/10.1002/cncr.31667DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6241518PMC
October 2018

Pleiotropic effects of n-6 and n-3 fatty acid-related genetic variants on circulating hemostatic variables.

Thromb Res 2018 08 1;168:53-59. Epub 2018 Jun 1.

Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, 1300 South Second Street, WBOB 300, Minneapolis, MN 55454, USA. Electronic address:

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http://dx.doi.org/10.1016/j.thromres.2018.05.032DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089352PMC
August 2018

Evaluation of the relationship between plasma lipids and abdominal aortic aneurysm: A Mendelian randomization study.

PLoS One 2018 12;13(4):e0195719. Epub 2018 Apr 12.

Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, Minnesota, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0195719PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5896990PMC
July 2018

Rare copy number variants identified in prune belly syndrome.

Eur J Med Genet 2018 Mar 23;61(3):145-151. Epub 2017 Nov 23.

Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, United States.

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http://dx.doi.org/10.1016/j.ejmg.2017.11.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5803418PMC
March 2018

Association between mitochondrial DNA copy number and sudden cardiac death: findings from the Atherosclerosis Risk in Communities study (ARIC).

Eur Heart J 2017 Dec;38(46):3443-3448

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, 733 N. Broadway, Miller Research Building, Room 459, Baltimore, MD 21205, USA.

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http://dx.doi.org/10.1093/eurheartj/ehx354DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5837579PMC
December 2017

Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease.

J Clin Endocrinol Metab 2017 08;102(8):2836-2843

Section on Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.

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http://dx.doi.org/10.1210/jc.2017-00161DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5546857PMC
August 2017

Loss-of-function mutations in the gene are a novel cause of Cushing's disease.

Endocr Relat Cancer 2017 08 22;24(8):379-392. Epub 2017 May 22.

Section on Endocrinology and GeneticsEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Bethesda, Maryland, USA

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http://dx.doi.org/10.1530/ERC-17-0131DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5510591PMC
August 2017

Failure to replicate thrombomodulin genetic variant predictors of venous thromboembolism in African Americans.

Blood 2017 08 15;130(5):688-690. Epub 2017 Jun 15.

Department of Laboratory Medicine and Pathology, School of Medicine, University of Minnesota, Minneapolis, MN.

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http://www.bloodjournal.org/lookup/doi/10.1182/blood-2017-03
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http://dx.doi.org/10.1182/blood-2017-03-771329DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542854PMC
August 2017

Corticotropinoma as a Component of Carney Complex.

J Endocr Soc 2017 Jul 30;1(7):918-925. Epub 2017 May 30.

Section on Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.

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http://dx.doi.org/10.1210/js.2017-00231DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686778PMC
July 2017

Identification of Genetic Variants Linking Protein C and Lipoprotein Metabolism: The ARIC Study (Atherosclerosis Risk in Communities).

Arterioscler Thromb Vasc Biol 2017 03 12;37(3):589-597. Epub 2017 Jan 12.

From the Division of Epidemiology and Community Health (J.S.P., W.T., L.-C.W., A.R.F.), Department of Laboratory Medicine and Pathology (N.P.), and Division of Biostatistics (W.G.), University of Minnesota, Minneapolis; Department of Medicine (M.C.) and Department of Pathology (M.C.), University of Vermont, Burlington; and Human Genetics Center and Institute of Molecular Medicine, University of Texas Health Science Center at Houston (E.B.).

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http://dx.doi.org/10.1161/ATVBAHA.116.308109DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376064PMC
March 2017

Heritability of Vascular Structure and Function: A Parent-Child Study.

J Am Heart Assoc 2017 02 2;6(2). Epub 2017 Feb 2.

Department of Pediatrics, University of Minnesota Medical School, Minneapolis, MN.

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http://dx.doi.org/10.1161/JAHA.116.004757DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5523771PMC
February 2017

Replication of genome-wide association signals in Asian Indians with early-onset type 2 diabetes.

Acta Diabetol 2016 Dec 4;53(6):915-923. Epub 2016 Aug 4.

Madras Diabetes Research Foundation, 4, Conran Smith Road, Gopalapuram, Chennai, 600 086, India.

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http://dx.doi.org/10.1007/s00592-016-0889-2DOI Listing
December 2016

Association between Mitochondrial DNA Copy Number in Peripheral Blood and Incident CKD in the Atherosclerosis Risk in Communities Study.

J Am Soc Nephrol 2016 08 21;27(8):2467-73. Epub 2016 Jan 21.

McKusick-Nathans Institute of Genetic Medicine and Department of Medicine, Division of Cardiology, Johns Hopkins School of Medicine, Baltimore, Maryland;

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http://dx.doi.org/10.1681/ASN.2015060661DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4978050PMC
August 2016

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.

Authors:
Nathalie Chami Ming-Huei Chen Andrew J Slater John D Eicher Evangelos Evangelou Salman M Tajuddin Latisha Love-Gregory Tim Kacprowski Ursula M Schick Akihiro Nomura Ayush Giri Samuel Lessard Jennifer A Brody Claudia Schurmann Nathan Pankratz Lisa R Yanek Ani Manichaikul Raha Pazoki Evelin Mihailov W David Hill Laura M Raffield Amber Burt Traci M Bartz Diane M Becker Lewis C Becker Eric Boerwinkle Jette Bork-Jensen Erwin P Bottinger Michelle L O'Donoghue David R Crosslin Simon de Denus Marie-Pierre Dubé Paul Elliott Gunnar Engström Michele K Evans James S Floyd Myriam Fornage He Gao Andreas Greinacher Vilmundur Gudnason Torben Hansen Tamara B Harris Caroline Hayward Jussi Hernesniemi Heather M Highland Joel N Hirschhorn Albert Hofman Marguerite R Irvin Mika Kähönen Ethan Lange Lenore J Launer Terho Lehtimäki Jin Li David C M Liewald Allan Linneberg Yongmei Liu Yingchang Lu Leo-Pekka Lyytikäinen Reedik Mägi Rasika A Mathias Olle Melander Andres Metspalu Nina Mononen Mike A Nalls Deborah A Nickerson Kjell Nikus Chris J O'Donnell Marju Orho-Melander Oluf Pedersen Astrid Petersmann Linda Polfus Bruce M Psaty Olli T Raitakari Emma Raitoharju Melissa Richard Kenneth M Rice Fernando Rivadeneira Jerome I Rotter Frank Schmidt Albert Vernon Smith John M Starr Kent D Taylor Alexander Teumer Betina H Thuesen Eric S Torstenson Russell P Tracy Ioanna Tzoulaki Neil A Zakai Caterina Vacchi-Suzzi Cornelia M van Duijn Frank J A van Rooij Mary Cushman Ian J Deary Digna R Velez Edwards Anne-Claire Vergnaud Lars Wallentin Dawn M Waterworth Harvey D White James G Wilson Alan B Zonderman Sekar Kathiresan Niels Grarup Tõnu Esko Ruth J F Loos Leslie A Lange Nauder Faraday Nada A Abumrad Todd L Edwards Santhi K Ganesh Paul L Auer Andrew D Johnson Alexander P Reiner Guillaume Lettre

Am J Hum Genet 2016 Jul 23;99(1):8-21. Epub 2016 Jun 23.

Department of Medicine, Université de Montréal, Montréal, QC H3T 1J4, Canada; Montreal Heart Institute, Montréal, QC H1T 1C8, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2016.05.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005438PMC
July 2016

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.

Authors:
John D Eicher Nathalie Chami Tim Kacprowski Akihiro Nomura Ming-Huei Chen Lisa R Yanek Salman M Tajuddin Ursula M Schick Andrew J Slater Nathan Pankratz Linda Polfus Claudia Schurmann Ayush Giri Jennifer A Brody Leslie A Lange Ani Manichaikul W David Hill Raha Pazoki Paul Elliot Evangelos Evangelou Ioanna Tzoulaki He Gao Anne-Claire Vergnaud Rasika A Mathias Diane M Becker Lewis C Becker Amber Burt David R Crosslin Leo-Pekka Lyytikäinen Kjell Nikus Jussi Hernesniemi Mika Kähönen Emma Raitoharju Nina Mononen Olli T Raitakari Terho Lehtimäki Mary Cushman Neil A Zakai Deborah A Nickerson Laura M Raffield Rakale Quarells Cristen J Willer Gina M Peloso Goncalo R Abecasis Dajiang J Liu Panos Deloukas Nilesh J Samani Heribert Schunkert Jeanette Erdmann Myriam Fornage Melissa Richard Jean-Claude Tardif John D Rioux Marie-Pierre Dube Simon de Denus Yingchang Lu Erwin P Bottinger Ruth J F Loos Albert Vernon Smith Tamara B Harris Lenore J Launer Vilmundur Gudnason Digna R Velez Edwards Eric S Torstenson Yongmei Liu Russell P Tracy Jerome I Rotter Stephen S Rich Heather M Highland Eric Boerwinkle Jin Li Ethan Lange James G Wilson Evelin Mihailov Reedik Mägi Joel Hirschhorn Andres Metspalu Tõnu Esko Caterina Vacchi-Suzzi Mike A Nalls Alan B Zonderman Michele K Evans Gunnar Engström Marju Orho-Melander Olle Melander Michelle L O'Donoghue Dawn M Waterworth Lars Wallentin Harvey D White James S Floyd Traci M Bartz Kenneth M Rice Bruce M Psaty J M Starr David C M Liewald Caroline Hayward Ian J Deary Andreas Greinacher Uwe Völker Thomas Thiele Henry Völzke Frank J A van Rooij André G Uitterlinden Oscar H Franco Abbas Dehghan Todd L Edwards Santhi K Ganesh Sekar Kathiresan Nauder Faraday Paul L Auer Alex P Reiner Guillaume Lettre Andrew D Johnson

Am J Hum Genet 2016 Jul 23;99(1):40-55. Epub 2016 Jun 23.

Population Sciences Branch, National Heart Lung and Blood Institute, The Framingham Heart Study, Framingham, MA 01702, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2016.05.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005441PMC
July 2016

Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.

Authors:
Salman M Tajuddin Ursula M Schick John D Eicher Nathalie Chami Ayush Giri Jennifer A Brody W David Hill Tim Kacprowski Jin Li Leo-Pekka Lyytikäinen Ani Manichaikul Evelin Mihailov Michelle L O'Donoghue Nathan Pankratz Raha Pazoki Linda M Polfus Albert Vernon Smith Claudia Schurmann Caterina Vacchi-Suzzi Dawn M Waterworth Evangelos Evangelou Lisa R Yanek Amber Burt Ming-Huei Chen Frank J A van Rooij James S Floyd Andreas Greinacher Tamara B Harris Heather M Highland Leslie A Lange Yongmei Liu Reedik Mägi Mike A Nalls Rasika A Mathias Deborah A Nickerson Kjell Nikus John M Starr Jean-Claude Tardif Ioanna Tzoulaki Digna R Velez Edwards Lars Wallentin Traci M Bartz Lewis C Becker Joshua C Denny Laura M Raffield John D Rioux Nele Friedrich Myriam Fornage He Gao Joel N Hirschhorn David C M Liewald Stephen S Rich Andre Uitterlinden Lisa Bastarache Diane M Becker Eric Boerwinkle Simon de Denus Erwin P Bottinger Caroline Hayward Albert Hofman Georg Homuth Ethan Lange Lenore J Launer Terho Lehtimäki Yingchang Lu Andres Metspalu Chris J O'Donnell Rakale C Quarells Melissa Richard Eric S Torstenson Kent D Taylor Anne-Claire Vergnaud Alan B Zonderman David R Crosslin Ian J Deary Marcus Dörr Paul Elliott Michele K Evans Vilmundur Gudnason Mika Kähönen Bruce M Psaty Jerome I Rotter Andrew J Slater Abbas Dehghan Harvey D White Santhi K Ganesh Ruth J F Loos Tõnu Esko Nauder Faraday James G Wilson Mary Cushman Andrew D Johnson Todd L Edwards Neil A Zakai Guillaume Lettre Alex P Reiner Paul L Auer

Am J Hum Genet 2016 Jul 23;99(1):22-39. Epub 2016 Jun 23.

Zilber School of Public Health, University of Wisconsin-Milwaukee, Milwaukee, WI 53205, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2016.05.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005433PMC
July 2016

Rare copy number variants implicated in posterior urethral valves.

Am J Med Genet A 2016 Mar 14;170(3):622-33. Epub 2015 Dec 14.

Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.

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http://dx.doi.org/10.1002/ajmg.a.37493DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205289PMC
March 2016

The associations between 6-n-propylthiouracil (PROP) intensity and taste intensities differ by TAS2R38 haplotype.

J Nutrigenet Nutrigenomics 2014 27;7(3):143-52. Epub 2015 Jan 27.

Departments of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, Wis., USA.

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http://dx.doi.org/10.1159/000371552DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322864PMC
October 2015

Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF.

Blood 2015 Sep 23;126(11):e19-29. Epub 2015 Jun 23.

Department of Epidemiology, and Group Health Research Institute, Group Health Cooperative, Seattle, WA; Seattle Epidemiologic Research and Information Center, Veterans Affairs Office of Research and Development, Seattle, WA.

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http://dx.doi.org/10.1182/blood-2015-02-624551DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4566813PMC
September 2015

Genetic and nongenetic risk factors for childhood cancer.

Pediatr Clin North Am 2015 Feb 18;62(1):11-25. Epub 2014 Oct 18.

Division of Epidemiology/Clinical Research, Department of Pediatrics, University of Minnesota, 420 Delaware Street, Southeast, Minneapolis, MN 55455, USA.

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http://dx.doi.org/10.1016/j.pcl.2014.09.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384439PMC
February 2015

Odor identification and cognitive function in the Beaver Dam Offspring Study.

J Clin Exp Neuropsychol 2013 21;35(7):669-76. Epub 2013 Jun 21.

a Department of Ophthalmology and Visual Sciences , University of Wisconsin School of Medicine and Public Health , Madison , WI , USA.

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http://dx.doi.org/10.1080/13803395.2013.809701DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778079PMC
April 2014

Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci.

Authors:
Vinicius Tragante Michael R Barnes Santhi K Ganesh Matthew B Lanktree Wei Guo Nora Franceschini Erin N Smith Toby Johnson Michael V Holmes Sandosh Padmanabhan Konrad J Karczewski Berta Almoguera John Barnard Jens Baumert Yen-Pei Christy Chang Clara C Elbers Martin Farrall Mary E Fischer Tom R Gaunt Johannes M I H Gho Christian Gieger Anuj Goel Yan Gong Aaron Isaacs Marcus E Kleber Irene Mateo Leach Caitrin W McDonough Matthijs F L Meijs Olle Melander Christopher P Nelson Ilja M Nolte Nathan Pankratz Tom S Price Jonathan Shaffer Sonia Shah Maciej Tomaszewski Peter J van der Most Erik P A Van Iperen Judith M Vonk Kate Witkowska Caroline O L Wong Li Zhang Amber L Beitelshees Gerald S Berenson Deepak L Bhatt Morris Brown Amber Burt Rhonda M Cooper-DeHoff John M Connell Karen J Cruickshanks Sean P Curtis George Davey-Smith Christian Delles Ron T Gansevoort Xiuqing Guo Shen Haiqing Claire E Hastie Marten H Hofker G Kees Hovingh Daniel S Kim Susan A Kirkland Barbara E Klein Ronald Klein Yun R Li Steffi Maiwald Christopher Newton-Cheh Eoin T O'Brien N Charlotte Onland-Moret Walter Palmas Afshin Parsa Brenda W Penninx Mary Pettinger Ramachandran S Vasan Jane E Ranchalis Paul M Ridker Lynda M Rose Peter Sever Daichi Shimbo Laura Steele Ronald P Stolk Barbara Thorand Mieke D Trip Cornelia M van Duijn W Monique Verschuren Cisca Wijmenga Sharon Wyatt J Hunter Young Aeilko H Zwinderman Connie R Bezzina Eric Boerwinkle Juan P Casas Mark J Caulfield Aravinda Chakravarti Daniel I Chasman Karina W Davidson Pieter A Doevendans Anna F Dominiczak Garret A FitzGerald John G Gums Myriam Fornage Hakon Hakonarson Indrani Halder Hans L Hillege Thomas Illig Gail P Jarvik Julie A Johnson John J P Kastelein Wolfgang Koenig Meena Kumari Winfried März Sarah S Murray Jeffery R O'Connell Albertine J Oldehinkel James S Pankow Daniel J Rader Susan Redline Muredach P Reilly Eric E Schadt Kandice Kottke-Marchant Harold Snieder Michael Snyder Alice V Stanton Martin D Tobin André G Uitterlinden Pim van der Harst Yvonne T van der Schouw Nilesh J Samani Hugh Watkins Andrew D Johnson Alex P Reiner Xiaofeng Zhu Paul I W de Bakker Daniel Levy Folkert W Asselbergs Patricia B Munroe Brendan J Keating

Am J Hum Genet 2014 Mar 20;94(3):349-60. Epub 2014 Feb 20.

Department of Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA; Center for Applied Genomics, Abramson Research Center, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2013.12.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951943PMC
March 2014

Low-Frequency Copy-Number Variants and General Cognitive Ability: No Evidence of Association.

Intelligence 2014 Jan;42:98-106

University of Minnesota Medical School, Department of Laboratory Medicine & Pathology, 420 Delaware St. SE, Minneapolis, MN 55455.

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http://dx.doi.org/10.1016/j.intell.2013.11.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909536PMC
January 2014

Factors related to fungiform papillae density: the beaver dam offspring study.

Chem Senses 2013 Oct 2;38(8):669-77. Epub 2013 Jul 2.

Department of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, WI, 53726, USA.

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http://dx.doi.org/10.1093/chemse/bjt033DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777560PMC
October 2013

An analysis of measures of effect size by age of onset in cancer genomewide association studies.

Genes Chromosomes Cancer 2013 Sep 14;52(9):855-9. Epub 2013 Jun 14.

Division of Academic General Pediatrics, Department of Pediatrics, University of Minnesota, Minneapolis, MN, 612-626-2134, USA.

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http://dx.doi.org/10.1002/gcc.22081DOI Listing
September 2013

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.

Authors:
Folkert W Asselbergs Yiran Guo Erik P A van Iperen Suthesh Sivapalaratnam Vinicius Tragante Matthew B Lanktree Leslie A Lange Berta Almoguera Yolande E Appelman John Barnard Jens Baumert Amber L Beitelshees Tushar R Bhangale Yii-Der Ida Chen Tom R Gaunt Yan Gong Jemma C Hopewell Toby Johnson Marcus E Kleber Taimour Y Langaee Mingyao Li Yun R Li Kiang Liu Caitrin W McDonough Matthijs F L Meijs Rita P S Middelberg Kiran Musunuru Christopher P Nelson Jeffery R O'Connell Sandosh Padmanabhan James S Pankow Nathan Pankratz Suzanne Rafelt Ramakrishnan Rajagopalan Simon P R Romaine Nicholas J Schork Jonathan Shaffer Haiqing Shen Erin N Smith Sam E Tischfield Peter J van der Most Jana V van Vliet-Ostaptchouk Niek Verweij Kelly A Volcik Li Zhang Kent R Bailey Kristian M Bailey Florianne Bauer Jolanda M A Boer Peter S Braund Amber Burt Paul R Burton Sarah G Buxbaum Wei Chen Rhonda M Cooper-Dehoff L Adrienne Cupples Jonas S deJong Christian Delles David Duggan Myriam Fornage Clement E Furlong Nicole Glazer John G Gums Claire Hastie Michael V Holmes Thomas Illig Susan A Kirkland Mika Kivimaki Ronald Klein Barbara E Klein Charles Kooperberg Kandice Kottke-Marchant Meena Kumari Andrea Z LaCroix Laya Mallela Gurunathan Murugesan Jose Ordovas Willem H Ouwehand Wendy S Post Richa Saxena Hubert Scharnagl Pamela J Schreiner Tina Shah Denis C Shields Daichi Shimbo Sathanur R Srinivasan Ronald P Stolk Daniel I Swerdlow Herman A Taylor Eric J Topol Elina Toskala Joost L van Pelt Jessica van Setten Salim Yusuf John C Whittaker A H Zwinderman Sonia S Anand Anthony J Balmforth Gerald S Berenson Connie R Bezzina Bernhard O Boehm Eric Boerwinkle Juan P Casas Mark J Caulfield Robert Clarke John M Connell Karen J Cruickshanks Karina W Davidson Ian N M Day Paul I W de Bakker Pieter A Doevendans Anna F Dominiczak Alistair S Hall Catharina A Hartman Christian Hengstenberg Hans L Hillege Marten H Hofker Steve E Humphries Gail P Jarvik Julie A Johnson Bernhard M Kaess Sekar Kathiresan Wolfgang Koenig Debbie A Lawlor Winfried März Olle Melander Braxton D Mitchell Grant W Montgomery Patricia B Munroe Sarah S Murray Stephen J Newhouse N Charlotte Onland-Moret Neil Poulter Bruce Psaty Susan Redline Stephen S Rich Jerome I Rotter Heribert Schunkert Peter Sever Alan R Shuldiner Roy L Silverstein Alice Stanton Barbara Thorand Mieke D Trip Michael Y Tsai Pim van der Harst Ellen van der Schoot Yvonne T van der Schouw W M Monique Verschuren Hugh Watkins Arthur A M Wilde Bruce H R Wolffenbuttel John B Whitfield G Kees Hovingh Christie M Ballantyne Cisca Wijmenga Muredach P Reilly Nicholas G Martin James G Wilson Daniel J Rader Nilesh J Samani Alex P Reiner Robert A Hegele John J P Kastelein Aroon D Hingorani Philippa J Talmud Hakon Hakonarson Clara C Elbers Brendan J Keating Fotios Drenos

Am J Hum Genet 2012 Nov 11;91(5):823-38. Epub 2012 Oct 11.

Department of Cardiology, Division of Heart and Lungs, University Medical Center Utrecht, Utrecht, The Netherlands.

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http://dx.doi.org/10.1016/j.ajhg.2012.08.032DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3487124PMC
November 2012

Joint analyses of disease and correlated quantitative phenotypes using next-generation sequencing data.

Genet Epidemiol 2011 ;35 Suppl 1:S67-73

Department of Genetics, Texas Biomedical Research Institute, San Antonio, Texas, USA.

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http://dx.doi.org/10.1002/gepi.20653DOI Listing
May 2012

Copy number variation in familial Parkinson disease.

PLoS One 2011 2;6(8):e20988. Epub 2011 Aug 2.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0020988PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3149037PMC
December 2011

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height.

Authors:
Matthew B Lanktree Yiran Guo Muhammed Murtaza Joseph T Glessner Swneke D Bailey N Charlotte Onland-Moret Guillaume Lettre Halit Ongen Ramakrishnan Rajagopalan Toby Johnson Haiqing Shen Christopher P Nelson Norman Klopp Jens Baumert Sandosh Padmanabhan Nathan Pankratz James S Pankow Sonia Shah Kira Taylor John Barnard Bas J Peters Cliona M Maloney Maximilian T Lobmeyer Alice Stanton M Hadi Zafarmand Simon P R Romaine Amar Mehta Erik P A van Iperen Yan Gong Tom S Price Erin N Smith Cecilia E Kim Yun R Li Folkert W Asselbergs Larry D Atwood Kristian M Bailey Deepak Bhatt Florianne Bauer Elijah R Behr Tushar Bhangale Jolanda M A Boer Bernhard O Boehm Jonathan P Bradfield Morris Brown Peter S Braund Paul R Burton Cara Carty Hareesh R Chandrupatla Wei Chen John Connell Chrysoula Dalgeorgou Anthonius de Boer Fotios Drenos Clara C Elbers James C Fang Caroline S Fox Edward C Frackelton Barry Fuchs Clement E Furlong Quince Gibson Christian Gieger Anuj Goel Diederik E Grobbee Claire Hastie Philip J Howard Guan-Hua Huang W Craig Johnson Qing Li Marcus E Kleber Barbara E K Klein Ronald Klein Charles Kooperberg Bonnie Ky Andrea Lacroix Paul Lanken Mark Lathrop Mingyao Li Vanessa Marshall Olle Melander Frank D Mentch Nuala J Meyer Keri L Monda Alexandre Montpetit Gurunathan Murugesan Karen Nakayama Dave Nondahl Abiodun Onipinla Suzanne Rafelt Stephen J Newhouse F George Otieno Sanjey R Patel Mary E Putt Santiago Rodriguez Radwan N Safa Douglas B Sawyer Pamela J Schreiner Claire Simpson Suthesh Sivapalaratnam Sathanur R Srinivasan Christine Suver Gary Swergold Nancy K Sweitzer Kelly A Thomas Barbara Thorand Nicholas J Timpson Sam Tischfield Martin Tobin Maciej Tomaszewski Maciej Tomaszweski W M Monique Verschuren Chris Wallace Bernhard Winkelmann Haitao Zhang Dongling Zheng Li Zhang Joseph M Zmuda Robert Clarke Anthony J Balmforth John Danesh Ian N Day Nicholas J Schork Paul I W de Bakker Christian Delles David Duggan Aroon D Hingorani Joel N Hirschhorn Marten H Hofker Steve E Humphries Mika Kivimaki Debbie A Lawlor Kandice Kottke-Marchant Jessica L Mega Braxton D Mitchell David A Morrow Jutta Palmen Susan Redline Denis C Shields Alan R Shuldiner Patrick M Sleiman George Davey Smith Martin Farrall Yalda Jamshidi David C Christiani Juan P Casas Alistair S Hall Pieter A Doevendans Jason D Christie Gerald S Berenson Sarah S Murray Thomas Illig Gerald W Dorn Thomas P Cappola Eric Boerwinkle Peter Sever Daniel J Rader Muredach P Reilly Mark Caulfield Philippa J Talmud Eric Topol James C Engert Kai Wang Anna Dominiczak Anders Hamsten Sean P Curtis Roy L Silverstein Leslie A Lange Marc S Sabatine Mieke Trip Danish Saleheen John F Peden Karen J Cruickshanks Winfried März Jeffrey R O'Connell Olaf H Klungel Cisca Wijmenga Anke Hilse Maitland-van der Zee Eric E Schadt Julie A Johnson Gail P Jarvik George J Papanicolaou Struan F A Grant Patricia B Munroe Kari E North Nilesh J Samani Wolfgang Koenig Tom R Gaunt Sonia S Anand Yvonne T van der Schouw Nicole Soranzo Garret A Fitzgerald Alex Reiner Robert A Hegele Hakon Hakonarson Brendan J Keating

Am J Hum Genet 2011 Jan 30;88(1):6-18. Epub 2010 Dec 30.

Department of Medicine and Biochemistry, University of Western Ontario, London, Ontario, N6A 5C1, Canada.

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http://dx.doi.org/10.1016/j.ajhg.2010.11.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3014369PMC
January 2011

Voxelwise genome-wide association study (vGWAS).

Neuroimage 2010 Nov 17;53(3):1160-74. Epub 2010 Feb 17.

Laboratory of Neuro Imaging, Department of Neurology, University of California, Los Angeles School of Medicine, Neuroscience Research Building 225E, 635 Charles Young Drive, Los Angeles, CA 90095-1769, USA.

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http://dx.doi.org/10.1016/j.neuroimage.2010.02.032DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2900429PMC
November 2010

Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease.

BMC Med Genet 2010 Apr 1;11:53. Epub 2010 Apr 1.

Department of Neurology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.

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http://dx.doi.org/10.1186/1471-2350-11-53DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858137PMC
April 2010

A two-stage classification approach identifies seven susceptibility genes for a simulated complex disease.

Authors:
Nathan Pankratz

BMC Proc 2007 18;1 Suppl 1:S30. Epub 2007 Dec 18.

Department of Medical and Molecular Genetics, 410 West 10th Street, HS4000, Indiana University, Indianapolis, Indiana 46202-3002, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2367605PMC
http://dx.doi.org/10.1186/1753-6561-1-s1-s30DOI Listing
December 2009

Non-redundant summary scores applied to the North American Rheumatoid Arthritis Consortium dataset.

BMC Proc 2009 Dec 15;3 Suppl 7:S39. Epub 2009 Dec 15.

Department of Medical and Molecular Genetics, Indiana University, School of Medicine, Indianapolis, Indiana 46202, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795937PMC
http://dx.doi.org/10.1186/1753-6561-3-s7-s39DOI Listing
December 2009

Alpha-synuclein and familial Parkinson's disease.

Mov Disord 2009 Jun;24(8):1125-31

Department of Medical and Molecular Genetics, Indiana University Medical Center, Indianapolis, Indiana 46202, USA.

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http://dx.doi.org/10.1002/mds.22524DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397145PMC
June 2009

Genomewide association study for susceptibility genes contributing to familial Parkinson disease.

Hum Genet 2009 Jan 6;124(6):593-605. Epub 2008 Nov 6.

Indiana University School of Medicine, Health Information and Translational Sciences Building, Indianapolis, IN 46202-3002, USA.

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http://dx.doi.org/10.1007/s00439-008-0582-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2627511PMC
January 2009

Clinical correlates of depressive symptoms in familial Parkinson's disease.

Mov Disord 2008 Nov;23(15):2216-23

Department of Medical and Molecular Genetics, Indiana University, Indianapolis, Indiana 46202, USA.

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http://dx.doi.org/10.1002/mds.22285DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2872794PMC
November 2008

Issues in association mapping with high-density SNP data and diverse family structures.

Genet Epidemiol 2007 ;31 Suppl 1:S22-33

Department of Genetic Epidemiology, Medical School, Georg-August-University Göttingen, Humboldtallee 32, D-37073 Göttingen, Germany.

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http://dx.doi.org/10.1002/gepi.20277DOI Listing
April 2008

Genetics of Parkinson disease.

Genet Med 2007 Dec;9(12):801-11

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana 46202-3002, USA.

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http://dx.doi.org/10.1097GIM.0b013e31815bf97cDOI Listing
December 2007

R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation.

Mov Disord 2007 Jan;22(2):254-7

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA.

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http://dx.doi.org/10.1002/mds.21233DOI Listing
January 2007

Chromosome 5 and Parkinson disease.

Eur J Hum Genet 2006 Oct 31;14(10):1106-10. Epub 2006 May 31.

Indiana University School of Medicine, Indianapolis, IN 46202-5251, USA.

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http://dx.doi.org/10.1038/sj.ejhg.5201666DOI Listing
October 2006

Hearing impairment susceptibility in elderly men and the DFNA18 locus.

Arch Otolaryngol Head Neck Surg 2006 May;132(5):506-10

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, USA.

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http://dx.doi.org/10.1001/archotol.132.5.506DOI Listing
May 2006

Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia.

Mov Disord 2006 Jan;21(1):45-9

Department of Medical and Molecular Genetics, Indiana University Medical Center, Indianapolis, Indiana, USA.

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http://dx.doi.org/10.1002/mds.20663DOI Listing
January 2006

Standard linkage and association methods identify the mechanism of four susceptibility genes for a simulated complex disease.

BMC Genet 2005 Dec 30;6 Suppl 1:S142. Epub 2005 Dec 30.

Department of Medical and Molecular Genetics, Indiana University, School of Medicine, Indianapolis, IN, USA.

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http://dx.doi.org/10.1186/1471-2156-6-S1-S142DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866793PMC
December 2005

The Familial Intracranial Aneurysm (FIA) study protocol.

BMC Med Genet 2005 Apr 26;6:17. Epub 2005 Apr 26.

Department of Neurology, University of Cincinnati, 231 Albert Sabin Way, Cincinnati, OH 45267-0525, USA.

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http://dx.doi.org/10.1186/1471-2350-6-17DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1097731PMC
April 2005

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.

Lancet 2005 Jan 29-Feb 4;365(9457):410-2

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.

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http://dx.doi.org/10.1016/S0140-6736(05)17828-3DOI Listing
February 2005

Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease.

Mov Disord 2004 Jun;19(6):649-55

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA.

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http://dx.doi.org/10.1002/mds.20097DOI Listing
June 2004

Genetics of Parkinson disease.

NeuroRx 2004 Apr;1(2):235-42

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana 46202-525, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC534935PMC
http://dx.doi.org/10.1602/neurorx.1.2.235DOI Listing
April 2004

Identification of genes for complex disease using longitudinal phenotypes.

BMC Genet 2003 Dec 31;4 Suppl 1:S58. Epub 2003 Dec 31.

Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA.

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http://dx.doi.org/10.1186/1471-2156-4-S1-S58DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866495PMC
December 2003

Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families.

Hum Mol Genet 2003 Oct 12;12(20):2599-608. Epub 2003 Aug 12.

Indiana University School of Medicine, Department of Medical and Molecular Genetics (IB 130), 975 West Walnut Street, Indianapolis, IN 46202-5251, USA.

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http://dx.doi.org/10.1093/hmg/ddg270DOI Listing
October 2003

Significant linkage of Parkinson disease to chromosome 2q36-37.

Am J Hum Genet 2003 Apr 13;72(4):1053-7. Epub 2003 Mar 13.

Department of Medical and Molecular Genetics, Indiana University Medical Center, Indianapolis, IN 46202, USA.

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http://dx.doi.org/10.1086/374383DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1180337PMC
April 2003