Joan E Bailey Wilson

Joan E Bailey Wilson

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Joan E Bailey Wilson

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Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencing.

Eur J Hum Genet 2019 Oct 21;27(10):1599-1610. Epub 2019 Jun 21.

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

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http://dx.doi.org/10.1038/s41431-019-0457-7DOI Listing
October 2019

Gene-based association analysis of survival traits via functional regression-based mixed effect cox models for related samples.

Genet Epidemiol 2019 Sep 10. Epub 2019 Sep 10.

Department of Biostatistics, Bioinformatics, and Biomathematics, Georgetown University Medical Center, Washington, District of Columbia.

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http://dx.doi.org/10.1002/gepi.22254DOI Listing
September 2019

Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33.

Hum Genet 2019 Apr 2;138(4):339-354. Epub 2019 Mar 2.

Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Dr, Suite 1200, Baltimore, MD, 21224, USA.

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http://dx.doi.org/10.1007/s00439-019-01991-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486401PMC
April 2019

ComPaSS-GWAS: A method to reduce type I error in genome-wide association studies when replication data are not available.

Genet Epidemiol 2019 02 18;43(1):102-111. Epub 2018 Oct 18.

Genometrics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute/National Institutes of Health (NHGRI/NIH), Baltimore, Maryland.

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http://dx.doi.org/10.1002/gepi.22168DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330131PMC
February 2019

A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1.

PLoS Genet 2018 08 13;14(8):e1007532. Epub 2018 Aug 13.

Division of Human Genetics, Department of Pediatrics, at The Children's Hospital of Philadelphia, and The Perelman School of Medicine at The University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.

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http://dx.doi.org/10.1371/journal.pgen.1007532DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107291PMC
August 2018

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error.

Authors:
Milly S Tedja Robert Wojciechowski Pirro G Hysi Nicholas Eriksson Nicholas A Furlotte Virginie J M Verhoeven Adriana I Iglesias Magda A Meester-Smoor Stuart W Tompson Qiao Fan Anthony P Khawaja Ching-Yu Cheng René Höhn Kenji Yamashiro Adam Wenocur Clare Grazal Toomas Haller Andres Metspalu Juho Wedenoja Jost B Jonas Ya Xing Wang Jing Xie Paul Mitchell Paul J Foster Barbara E K Klein Ronald Klein Andrew D Paterson S Mohsen Hosseini Rupal L Shah Cathy Williams Yik Ying Teo Yih Chung Tham Preeti Gupta Wanting Zhao Yuan Shi Woei-Yuh Saw E-Shyong Tai Xue Ling Sim Jennifer E Huffman Ozren Polašek Caroline Hayward Goran Bencic Igor Rudan James F Wilson Peter K Joshi Akitaka Tsujikawa Fumihiko Matsuda Kristina N Whisenhunt Tanja Zeller Peter J van der Spek Roxanna Haak Hanne Meijers-Heijboer Elisabeth M van Leeuwen Sudha K Iyengar Jonathan H Lass Albert Hofman Fernando Rivadeneira André G Uitterlinden Johannes R Vingerling Terho Lehtimäki Olli T Raitakari Ginevra Biino Maria Pina Concas Tae-Hwi Schwantes-An Robert P Igo Gabriel Cuellar-Partida Nicholas G Martin Jamie E Craig Puya Gharahkhani Katie M Williams Abhishek Nag Jugnoo S Rahi Phillippa M Cumberland Cécile Delcourt Céline Bellenguez Janina S Ried Arthur A Bergen Thomas Meitinger Christian Gieger Tien Yin Wong Alex W Hewitt David A Mackey Claire L Simpson Norbert Pfeiffer Olavi Pärssinen Paul N Baird Veronique Vitart Najaf Amin Cornelia M van Duijn Joan E Bailey-Wilson Terri L Young Seang-Mei Saw Dwight Stambolian Stuart MacGregor Jeremy A Guggenheim Joyce Y Tung Christopher J Hammond Caroline C W Klaver

Nat Genet 2018 06 28;50(6):834-848. Epub 2018 May 28.

Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands.

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http://www.nature.com/articles/s41588-018-0127-7
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http://dx.doi.org/10.1038/s41588-018-0127-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980758PMC
June 2018

Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p.

Invest Ophthalmol Vis Sci 2017 07;58(9):3547-3554

Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, Maryland, United States.

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http://dx.doi.org/10.1167/iovs.16-21271DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5510992PMC
July 2017

Rare copy number variants in patients with congenital conotruncal heart defects.

Birth Defects Res 2017 Mar 13;109(4):271-295. Epub 2017 Feb 13.

Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

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http://dx.doi.org/10.1002/bdra.23609DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5407323PMC
March 2017

A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing.

Genet Epidemiol 2017 Jan 5;41(1):18-34. Epub 2016 Dec 5.

Biostatistics and Bioinformatics Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health (NIH), Bethesda, MD, USA.

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http://dx.doi.org/10.1002/gepi.22014DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154843PMC
January 2017

A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits.

Genet Epidemiol 2016 Dec 4;40(8):702-721. Epub 2016 Jul 4.

Human Genetics Center, University of Texas-Houston, Houston, Texas, United States of America.

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http://dx.doi.org/10.1002/gepi.21984DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567849PMC
December 2016

Comparison of parametric and machine methods for variable selection in simulated Genetic Analysis Workshop 19 data.

BMC Proc 2016 18;10(Suppl 7):147-152. Epub 2016 Oct 18.

Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Drive, Suite 1200, Baltimore, MD 21224 USA.

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http://dx.doi.org/10.1186/s12919-016-0021-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133476PMC
October 2016

Variable selection method for the identification of epistatic models.

Pac Symp Biocomput 2015 :195-206

Computational and Statistical Genomics Branch (NHGRI, NIH), Baltimore, MD 21224, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299919PMC
April 2016

Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error.

Authors:
Qiao Fan Virginie J M Verhoeven Robert Wojciechowski Veluchamy A Barathi Pirro G Hysi Jeremy A Guggenheim René Höhn Veronique Vitart Anthony P Khawaja Kenji Yamashiro S Mohsen Hosseini Terho Lehtimäki Yi Lu Toomas Haller Jing Xie Cécile Delcourt Mario Pirastu Juho Wedenoja Puya Gharahkhani Cristina Venturini Masahiro Miyake Alex W Hewitt Xiaobo Guo Johanna Mazur Jenifer E Huffman Katie M Williams Ozren Polasek Harry Campbell Igor Rudan Zoran Vatavuk James F Wilson Peter K Joshi George McMahon Beate St Pourcain David M Evans Claire L Simpson Tae-Hwi Schwantes-An Robert P Igo Alireza Mirshahi Audrey Cougnard-Gregoire Céline Bellenguez Maria Blettner Olli Raitakari Mika Kähönen Ilkka Seppala Tanja Zeller Thomas Meitinger Janina S Ried Christian Gieger Laura Portas Elisabeth M van Leeuwen Najaf Amin André G Uitterlinden Fernando Rivadeneira Albert Hofman Johannes R Vingerling Ya Xing Wang Xu Wang Eileen Tai-Hui Boh M Kamran Ikram Charumathi Sabanayagam Preeti Gupta Vincent Tan Lei Zhou Candice E H Ho Wan'e Lim Roger W Beuerman Rosalynn Siantar E-Shyong Tai Eranga Vithana Evelin Mihailov Chiea-Chuen Khor Caroline Hayward Robert N Luben Paul J Foster Barbara E K Klein Ronald Klein Hoi-Suen Wong Paul Mitchell Andres Metspalu Tin Aung Terri L Young Mingguang He Olavi Pärssinen Cornelia M van Duijn Jie Jin Wang Cathy Williams Jost B Jonas Yik-Ying Teo David A Mackey Konrad Oexle Nagahisa Yoshimura Andrew D Paterson Norbert Pfeiffer Tien-Yin Wong Paul N Baird Dwight Stambolian Joan E Bailey Wilson Ching-Yu Cheng Christopher J Hammond Caroline C W Klaver Seang-Mei Saw Jugnoo S Rahi Jean-François Korobelnik John P Kemp Nicholas J Timpson George Davey Smith Jamie E Craig Kathryn P Burdon Rhys D Fogarty Sudha K Iyengar Emily Chew Sarayut Janmahasatian Nicholas G Martin Stuart MacGregor Liang Xu Maria Schache Vinay Nangia Songhomitra Panda-Jonas Alan F Wright Jeremy R Fondran Jonathan H Lass Sheng Feng Jing Hua Zhao Kay-Tee Khaw Nick J Wareham Taina Rantanen Jaakko Kaprio Chi Pui Pang Li Jia Chen Pancy O Tam Vishal Jhanji Alvin L Young Angela Döring Leslie J Raffel Mary-Frances Cotch Xiaohui Li Shea Ping Yip Maurice K H Yap Ginevra Biino Simona Vaccargiu Maurizio Fossarello Brian Fleck Seyhan Yazar Jan Willem L Tideman Milly Tedja Margaret M Deangelis Margaux Morrison Lindsay Farrer Xiangtian Zhou Wei Chen Nobuhisa Mizuki Akira Meguro Kari Matti Mäkelä

Nat Commun 2016 Mar 29;7:11008. Epub 2016 Mar 29.

Department of Ophthalmology, Erasmus Medical Center, 3000 CA Rotterdam, The Netherlands.

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http://dx.doi.org/10.1038/ncomms11008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820539PMC
March 2016

r2VIM: A new variable selection method for random forests in genome-wide association studies.

BioData Min 2016 1;9. Epub 2016 Feb 1.

Statistical Genetics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Dr, 21224 Baltimore, USA.

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http://dx.doi.org/10.1186/s13040-016-0087-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736152PMC
February 2016

High incidence of unrecognized visceral/neurological late-onset Niemann-Pick disease, type C1, predicted by analysis of massively parallel sequencing data sets.

Genet Med 2016 Jan 12;18(1):41-8. Epub 2015 Mar 12.

Program in Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1038/gim.2015.25DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4486368PMC
January 2016

Gene-Gene Interaction Among WNT Genes for Oral Cleft in Trios.

Genet Epidemiol 2015 Jul 6;39(5):385-94. Epub 2015 Feb 6.

Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, Maryland, United States of America.

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http://doi.wiley.com/10.1002/gepi.21888
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http://dx.doi.org/10.1002/gepi.21888DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469492PMC
July 2015

Pleiotropy analysis of quantitative traits at gene level by multivariate functional linear models.

Genet Epidemiol 2015 May 23;39(4):259-75. Epub 2015 Mar 23.

Biostatistics and Bioinformatics Branch, Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, United States of America.

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http://dx.doi.org/10.1002/gepi.21895DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443751PMC
May 2015

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.

Hum Genet 2015 Feb 4;134(2):131-46. Epub 2014 Nov 4.

National Human Genome Research Institute, National Institutes of Health, 333 Cassell Drive Suite 1200, Baltimore, MD, 21224, USA.

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http://dx.doi.org/10.1007/s00439-014-1500-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4291519PMC
February 2015

A recurrent mutation in PARK2 is associated with familial lung cancer.

Am J Hum Genet 2015 Feb 29;96(2):301-8. Epub 2015 Jan 29.

Department of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, WI 53226, USA; Cancer Center, Medical College of Wisconsin, Milwaukee, WI 53226, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2014.12.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320264PMC
February 2015

8q24 risk alleles and prostate cancer in African-Barbadian men.

Prostate 2014 Dec 22;74(16):1579-88. Epub 2014 Sep 22.

Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, Maryland.

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http://dx.doi.org/10.1002/pros.22871DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322001PMC
December 2014

False-positive rates in two-point parametric linkage analysis.

BMC Proc 2014 17;8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S110. Epub 2014 Jun 17.

Statistical Genetics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Drive, Suite 1200, Baltimore, MD 21224, USA.

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http://dx.doi.org/10.1186/1753-6561-8-S1-S110DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143621PMC
December 2014

Generalized functional linear models for gene-based case-control association studies.

Genet Epidemiol 2014 Nov 9;38(7):622-637. Epub 2014 Sep 9.

Human Genetics Center, University of Texas - Houston P.O. Box 20334, Houston, Texas 77225.

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http://dx.doi.org/10.1002/gepi.21840DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189986PMC
November 2014

Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma.

Nat Genet 2014 Oct 31;46(10):1126-1130. Epub 2014 Aug 31.

Singapore Eye Research Institute, Singapore National Eye Centre, Singapore.

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http://dx.doi.org/10.1038/ng.3087DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177225PMC
October 2014

Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives.

Bioinformatics 2014 Aug 16;30(15):2189-96. Epub 2014 Apr 16.

Centre de Recherche de l'Institut Universitaire en Santé Mentale de Québec, G1J 2G3, Département de Médecine Sociale et Préventive, Université Laval, Québec, G1V 0A6 Canada, Department of Biostatistics, Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD 21224, Department of Oral Biology, Center for Craniofacial and Dental Genetics, School of Dental Medicine, University of Pittsburgh, PA 15219, Department of Pediatrics, School of Medicine, University of Iowa, IA 52242, USA, Institute of Human Genetics, University of Bonn, Bonn D-53127, Germany and Dr. Hejazi Clinic, P.O. Box 2519, Riyadh 11461, Saudi Arabia.

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http://bioinformatics.oxfordjournals.org/content/early/2014/
Web Search
http://bioinformatics.oxfordjournals.org/cgi/doi/10.1093/bio
Publisher Site
http://dx.doi.org/10.1093/bioinformatics/btu198DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103601PMC
August 2014

Regional replication of association with refractive error on 15q14 and 15q25 in the Age-Related Eye Disease Study cohort.

Mol Vis 2013 2;19:2173-86. Epub 2013 Nov 2.

Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3826323PMC
March 2014

Risk estimation using probability machines.

BioData Min 2014 Mar 1;7(1). Epub 2014 Mar 1.

Clinical Trials and Outcomes Branch, National Institute of Arthritis, Musculoskeletal and Skin Diseases, National Institutes of Health, Room 4-1350, Bldg 10 CRC, 10 Center Drive, Bethesda, MD 20892-1468, USA.

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http://dx.doi.org/10.1186/1756-0381-7-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015350PMC
March 2014

Functional linear models for association analysis of quantitative traits.

Genet Epidemiol 2013 Nov;37(7):726-42

Biostatistics and Bioinformatics Branch, Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Rockville, Maryland, United States of America.

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http://dx.doi.org/10.1002/gepi.21757DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163942PMC
November 2013

Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error.

Authors:
Ching-Yu Cheng Maria Schache M Kamran Ikram Terri L Young Jeremy A Guggenheim Veronique Vitart Stuart MacGregor Virginie J M Verhoeven Veluchamy A Barathi Jiemin Liao Pirro G Hysi Joan E Bailey-Wilson Beate St Pourcain John P Kemp George McMahon Nicholas J Timpson David M Evans Grant W Montgomery Aniket Mishra Ya Xing Wang Jie Jin Wang Elena Rochtchina Ozren Polasek Alan F Wright Najaf Amin Elisabeth M van Leeuwen James F Wilson Craig E Pennell Cornelia M van Duijn Paulus T V M de Jong Johannes R Vingerling Xin Zhou Peng Chen Ruoying Li Wan-Ting Tay Yingfeng Zheng Merwyn Chew Kathryn P Burdon Jamie E Craig Sudha K Iyengar Robert P Igo Jonathan H Lass Emily Y Chew Toomas Haller Evelin Mihailov Andres Metspalu Juho Wedenoja Claire L Simpson Robert Wojciechowski René Höhn Alireza Mirshahi Tanja Zeller Norbert Pfeiffer Karl J Lackner Thomas Bettecken Thomas Meitinger Konrad Oexle Mario Pirastu Laura Portas Abhishek Nag Katie M Williams Ekaterina Yonova-Doing Ronald Klein Barbara E Klein S Mohsen Hosseini Andrew D Paterson Kari-Matti Makela Terho Lehtimaki Mika Kahonen Olli Raitakari Nagahisa Yoshimura Fumihiko Matsuda Li Jia Chen Chi Pui Pang Shea Ping Yip Maurice K H Yap Akira Meguro Nobuhisa Mizuki Hidetoshi Inoko Paul J Foster Jing Hua Zhao Eranga Vithana E-Shyong Tai Qiao Fan Liang Xu Harry Campbell Brian Fleck Igor Rudan Tin Aung Albert Hofman André G Uitterlinden Goran Bencic Chiea-Chuen Khor Hannah Forward Olavi Pärssinen Paul Mitchell Fernando Rivadeneira Alex W Hewitt Cathy Williams Ben A Oostra Yik-Ying Teo Christopher J Hammond Dwight Stambolian David A Mackey Caroline C W Klaver Tien-Yin Wong Seang-Mei Saw Paul N Baird

Am J Hum Genet 2013 Aug;93(2):264-77

Department of Ophthalmology, National University of Singapore and National University Health System, Singapore 119228, Singapore; Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore 117597, Singapore; Singapore Eye Research Institute, Singapore National Eye Centre, Singapore 168751, Singapore; Centre for Quantitative Medicine, Office of Clinical Sciences, Duke-National University of Singapore Graduate Medical School, Singapore 169857, Singapore.

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http://dx.doi.org/10.1016/j.ajhg.2013.06.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772747PMC
August 2013

Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis.

Eur J Hum Genet 2013 Apr 5;21(4):437-43. Epub 2012 Sep 5.

Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA.

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http://dx.doi.org/10.1038/ejhg.2012.185DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598326PMC
April 2013

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.

Authors:
Virginie J M Verhoeven Pirro G Hysi Robert Wojciechowski Qiao Fan Jeremy A Guggenheim René Höhn Stuart MacGregor Alex W Hewitt Abhishek Nag Ching-Yu Cheng Ekaterina Yonova-Doing Xin Zhou M Kamran Ikram Gabriëlle H S Buitendijk George McMahon John P Kemp Beate St Pourcain Claire L Simpson Kari-Matti Mäkelä Terho Lehtimäki Mika Kähönen Andrew D Paterson S Mohsen Hosseini Hoi Suen Wong Liang Xu Jost B Jonas Olavi Pärssinen Juho Wedenoja Shea Ping Yip Daniel W H Ho Chi Pui Pang Li Jia Chen Kathryn P Burdon Jamie E Craig Barbara E K Klein Ronald Klein Toomas Haller Andres Metspalu Chiea-Chuen Khor E-Shyong Tai Tin Aung Eranga Vithana Wan-Ting Tay Veluchamy A Barathi Peng Chen Ruoying Li Jiemin Liao Yingfeng Zheng Rick T Ong Angela Döring David M Evans Nicholas J Timpson Annemieke J M H Verkerk Thomas Meitinger Olli Raitakari Felicia Hawthorne Tim D Spector Lennart C Karssen Mario Pirastu Federico Murgia Wei Ang Aniket Mishra Grant W Montgomery Craig E Pennell Phillippa M Cumberland Ioana Cotlarciuc Paul Mitchell Jie Jin Wang Maria Schache Sarayut Janmahasatian Sarayut Janmahasathian Robert P Igo Jonathan H Lass Emily Chew Sudha K Iyengar Theo G M F Gorgels Igor Rudan Caroline Hayward Alan F Wright Ozren Polasek Zoran Vatavuk James F Wilson Brian Fleck Tanja Zeller Alireza Mirshahi Christian Müller André G Uitterlinden Fernando Rivadeneira Johannes R Vingerling Albert Hofman Ben A Oostra Najaf Amin Arthur A B Bergen Yik-Ying Teo Jugnoo S Rahi Veronique Vitart Cathy Williams Paul N Baird Tien-Yin Wong Konrad Oexle Norbert Pfeiffer David A Mackey Terri L Young Cornelia M van Duijn Seang-Mei Saw Joan E Bailey-Wilson Dwight Stambolian Caroline C Klaver Christopher J Hammond

Nat Genet 2013 Mar 10;45(3):314-8. Epub 2013 Feb 10.

Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1038/ng.2554DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3740568PMC
March 2013

Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium.

Authors:
Virginie J M Verhoeven Pirro G Hysi Seang-Mei Saw Veronique Vitart Alireza Mirshahi Jeremy A Guggenheim Mary Frances Cotch Kenji Yamashiro Paul N Baird David A Mackey Robert Wojciechowski M Kamran Ikram Alex W Hewitt Priya Duggal Sarayut Janmahasatian Chiea-Chuen Khor Qiao Fan Xin Zhou Terri L Young E-Shyong Tai Liang-Kee Goh Yi-Ju Li Tin Aung Eranga Vithana Yik-Ying Teo Wanting Tay Xueling Sim Igor Rudan Caroline Hayward Alan F Wright Ozren Polasek Harry Campbell James F Wilson Brian W Fleck Isao Nakata Nagahisa Yoshimura Ryo Yamada Fumihiko Matsuda Kyoko Ohno-Matsui Abhishek Nag George McMahon Beate St Pourcain Yi Lu Jugnoo S Rahi Phillippa M Cumberland Shomi Bhattacharya Claire L Simpson Larry D Atwood Xiaohui Li Leslie J Raffel Federico Murgia Laura Portas Dominiek D G Despriet Leonieke M E van Koolwijk Christian Wolfram Karl J Lackner Anke Tönjes Reedik Mägi Terho Lehtimäki Mika Kähönen Tõnu Esko Andres Metspalu Taina Rantanen Olavi Pärssinen Barbara E Klein Thomas Meitinger Timothy D Spector Ben A Oostra Albert V Smith Paulus T V M de Jong Albert Hofman Najaf Amin Lennart C Karssen Fernando Rivadeneira Johannes R Vingerling Guðný Eiríksdóttir Vilmundur Gudnason Angela Döring Thomas Bettecken André G Uitterlinden Cathy Williams Tanja Zeller Raphaële Castagné Konrad Oexle Cornelia M van Duijn Sudha K Iyengar Paul Mitchell Jie Jin Wang René Höhn Norbert Pfeiffer Joan E Bailey-Wilson Dwight Stambolian Tien-Yin Wong Christopher J Hammond Caroline C W Klaver

Hum Genet 2012 Sep 5;131(9):1467-80. Epub 2012 Jun 5.

Department of Ophthalmology, Erasmus Medical Center, 3000 CA Rotterdam, The Netherlands.

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http://dx.doi.org/10.1007/s00439-012-1176-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3418496PMC
September 2012

Suggestive evidence of linkage identified at chromosomes 12q24 and 2p16 in African American prostate cancer families from Louisiana.

Prostate 2012 Jun 5;72(9):938-47. Epub 2011 Oct 5.

Department of Genetics, Louisiana State University Health Sciences Center, New Orleans, Louisiana 70112, USA.

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http://dx.doi.org/10.1002/pros.21496DOI Listing
June 2012

Brief review of regression-based and machine learning methods in genetic epidemiology: the Genetic Analysis Workshop 17 experience.

Genet Epidemiol 2011 ;35 Suppl 1:S5-11

Clinical Sciences Section, National Institute of Arthritis, Musculoskeletal, and Skin Diseases, National Institutes of Health, Bethesda, MD 21224, USA.

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http://dx.doi.org/10.1002/gepi.20642DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3345521PMC
May 2012

Linkage analysis in the next-generation sequencing era.

Hum Hered 2011 23;72(4):228-36. Epub 2011 Dec 23.

Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD 21224, USA.

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http://dx.doi.org/10.1159/000334381DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3267991PMC
April 2012

Dissecting the genetic heterogeneity of myopia susceptibility in an Ashkenazi Jewish population using ordered subset analysis.

Mol Vis 2011 17;17:1641-51. Epub 2011 Jun 17.

1nherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD 21224, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3123157PMC
November 2011

Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data.

BMC Proc 2011 Nov 29;5 Suppl 9:S83. Epub 2011 Nov 29.

Statistical Genetics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 31 Center Drive, 333 Cassell Drive Suite 1200, Baltimore, MD 21224, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287924PMC
November 2011

Performance of random forests and logic regression methods using mini-exome sequence data.

BMC Proc 2011 Nov 29;5 Suppl 9:S104. Epub 2011 Nov 29.

Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD 21224, USA.

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http://dx.doi.org/10.1186/1753-6561-5-S9-S104DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287827PMC
November 2011

Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression.

BMC Proc 2011 Nov 29;5 Suppl 9:S15. Epub 2011 Nov 29.

Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Drive, Baltimore, MD 21224, USA.

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http://dx.doi.org/10.1186/1753-6561-5-S9-S15DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287849PMC
November 2011

Linkage analysis of quantitative refraction and refractive errors in the Beaver Dam Eye Study.

Invest Ophthalmol Vis Sci 2011 Jul 13;52(8):5220-5. Epub 2011 Jul 13.

Department of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.

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http://dx.doi.org/10.1167/iovs.10-7096DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176073PMC
July 2011

Ordered subset analysis identifies loci influencing lung cancer risk on chromosomes 6q and 12q.

Cancer Epidemiol Biomarkers Prev 2010 Dec 28;19(12):3157-66. Epub 2010 Oct 28.

Department of Epidemiology, The University of Texas, MD Anderson Cancer Center, Houston, Texas 77030, USA.

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http://dx.doi.org/10.1158/1055-9965.EPI-10-0792DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249234PMC
December 2010

Contribution of HPC1 (RNASEL) and HPCX variants to prostate cancer in a founder population.

Prostate 2010 Nov;70(15):1716-27

Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, New York 10461, USA.

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http://dx.doi.org/10.1002/pros.21207DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3404133PMC
November 2010

Association of matrix metalloproteinase gene polymorphisms with refractive error in Amish and Ashkenazi families.

Invest Ophthalmol Vis Sci 2010 Oct 19;51(10):4989-95. Epub 2010 May 19.

Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, Maryland 21224, USA.

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http://dx.doi.org/10.1167/iovs.10-5474DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3066601PMC
October 2010

Admixture mapping of obesity-related traits in African Americans: the Atherosclerosis Risk in Communities (ARIC) Study.

Obesity (Silver Spring) 2010 Mar 20;18(3):563-72. Epub 2009 Aug 20.

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.

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http://dx.doi.org/10.1038/oby.2009.282DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2866099PMC
March 2010

Genome-wide linkage analysis of multiple metabolic factors: evidence of genetic heterogeneity.

Obesity (Silver Spring) 2010 Jan 14;18(1):146-52. Epub 2009 May 14.

Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, Maryland, USA.

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http://dx.doi.org/10.1038/oby.2009.142DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2866100PMC
January 2010

Normalization of microarray expression data using within-pedigree pool and its effect on linkage analysis.

BMC Proc 2007 18;1 Suppl 1:S152. Epub 2007 Dec 18.

Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Drive, Suite 1200, Baltimore, Maryland 21224, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2367611PMC
http://dx.doi.org/10.1186/1753-6561-1-s1-s152DOI Listing
December 2009

Application of sex-specific single-nucleotide polymorphism filters in genome-wide association data.

BMC Proc 2009 Dec 15;3 Suppl 7:S57. Epub 2009 Dec 15.

Center for Inherited Disease Research, Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21224, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795957PMC
http://dx.doi.org/10.1186/1753-6561-3-s7-s57DOI Listing
December 2009

Evaluation of random forests performance for genome-wide association studies in the presence of interaction effects.

BMC Proc 2009 Dec 15;3 Suppl 7:S64. Epub 2009 Dec 15.

National Human Genome Research Institute, National Institutes of Health, 333 Cassell Drive, Baltimore, MD 21224, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795965PMC
http://dx.doi.org/10.1186/1753-6561-3-s7-s64DOI Listing
December 2009

Fine-mapping of candidate region in Amish and Ashkenazi families confirms linkage of refractive error to a QTL on 1p34-p36.

Mol Vis 2009 Jul 17;15:1398-406. Epub 2009 Jul 17.

Inherited Disease Research Branch, National Human Genome Research Institute, 333 Cassell Drive, Baltimore, MD 21224, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2713730PMC
July 2009

Genomewide linkage scans for ocular refraction and meta-analysis of four populations in the Myopia Family Study.

Invest Ophthalmol Vis Sci 2009 May 17;50(5):2024-32. Epub 2009 Jan 17.

Inherited Disease Research Branch, National Human Genome Research Institute, Baltimore, Maryland 21231, USA.

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http://iovs.arvojournals.org/article.aspx?doi=10.1167/iovs.0
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http://dx.doi.org/10.1167/iovs.08-2848DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2885973PMC
May 2009

Genome-wide scan of African-American and white families for linkage to myopia.

Am J Ophthalmol 2009 Mar 20;147(3):512-517.e2. Epub 2008 Nov 20.

Pennsylvania College of Optometry, Philadelphia, USA.

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http://dx.doi.org/10.1016/j.ajo.2008.09.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4152232PMC
March 2009

Establishing an adjusted p-value threshold to control the family-wide type 1 error in genome wide association studies.

BMC Genomics 2008 Oct 31;9:516. Epub 2008 Oct 31.

Statistical Genetics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD USA.

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http://bmcgenomics.biomedcentral.com/articles/10.1186/1471-2
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http://dx.doi.org/10.1186/1471-2164-9-516DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2621212PMC
October 2008