Alexander F Wilson

Alexander F Wilson

UNVERIFIED PROFILE

Are you Alexander F Wilson?   Register this Author

Register author
Alexander F Wilson

Alexander F Wilson

Publications by authors named "Alexander F Wilson"

Are you Alexander F Wilson?   Register this Author

63Publications

1201Reads

11Profile Views

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.

View Article

Download full-text PDF

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

View Article

Download full-text PDF

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

Genetic associations with childhood brain growth, defined in two longitudinal cohorts.

Genet Epidemiol 2018 06 22;42(4):405-414. Epub 2018 Apr 22.

Section on Neurobehavioral Clinical Research, Social and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, Maryland, United States of America.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/gepi.22122DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980751PMC
June 2018

A variant associated with sagittal nonsyndromic craniosynostosis alters the regulatory function of a non-coding element.

Am J Med Genet A 2017 Nov 6;173(11):2893-2897. Epub 2017 Oct 6.

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

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.38392DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5659764PMC
November 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.

View Article

Download full-text PDF

Source
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.

View Article

Download full-text PDF

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

Type I error rates of rare single nucleotide variants are inflated in tests of association with non-normally distributed traits using simple linear regression methods.

BMC Proc 2016 18;10(Suppl 7):385-388. Epub 2016 Oct 18.

Genometrics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD 21224 USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/s12919-016-0060-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133479PMC
October 2016

Evaluation of IRX Genes and Conserved Noncoding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis.

G3 (Bethesda) 2016 06 1;6(6):1707-12. Epub 2016 Jun 1.

Genometrics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, Maryland 21224.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1534/g3.116.029975DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889666PMC
June 2016

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.

View Article

Download full-text PDF

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

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.

View Article

Download full-text PDF

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

Genetic modifiers of neurofibromatosis type 1-associated café-au-lait macule count identified using multi-platform analysis.

PLoS Genet 2014 Oct 16;10(10):e1004575. Epub 2014 Oct 16.

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland, United States of America.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1371/journal.pgen.1004575DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199479PMC
October 2014

Targeted deep resequencing identifies coding variants in the PEAR1 gene that play a role in platelet aggregation.

PLoS One 2013 21;8(5):e64179. Epub 2013 May 21.

Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, Maryland, United States of America.

View Article

Download full-text PDF

Source
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0064179PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660448PMC
December 2013

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.

View Article

Download full-text PDF

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

CHD7 gene polymorphisms and familial idiopathic scoliosis.

Spine (Phila Pa 1976) 2013 Oct;38(22):E1432-6

*Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD †Department of Orthopaedic Surgery, University of Colorado Denver Anschutz Medical Campus, Aurora, CO; and ‡Center for Inherited Disease Research, Institute of Genetic Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/BRS.0b013e3182a51781DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3881965PMC
October 2013

The robustness of generalized estimating equations for association tests in extended family data.

Hum Hered 2012 3;74(1):17-26. Epub 2012 Oct 3.

Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD 21205, USA.

View Article

Download full-text PDF

Source
https://www.karger.com/Article/FullText/341636
Publisher Site
http://dx.doi.org/10.1159/000341636DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3736986PMC
April 2013

The stat3/socs3a pathway is a key regulator of hair cell regeneration in zebrafish. [corrected].

J Neurosci 2012 Aug;32(31):10662-73

Genome Technology Branch, and Inherited Disease Research Branch, National Human Genome Research Institute, Bethesda, Maryland 20892, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1523/JNEUROSCI.5785-10.2012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3427933PMC
August 2012

Lessons learned from Genetic Analysis Workshop 17: transitioning from genome-wide association studies to whole-genome statistical genetic analysis.

Genet Epidemiol 2011 ;35 Suppl 1:S107-14

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

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/gepi.20659DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3277851PMC
May 2012

Quality control issues and the identification of rare functional variants with next-generation sequencing data.

Genet Epidemiol 2011 ;35 Suppl 1:S22-8

Institut für Medizinische Biometrie und Statistik, Universität zu Lübeck, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/gepi.20645DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3268158PMC
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.

View Article

Download full-text PDF

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

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.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/1753-6561-5-S9-S83DOI Listing
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.

View Article

Download full-text PDF

Source
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.

View Article

Download full-text PDF

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

Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.

Authors:
Themistocles L Assimes Hilma Hólm Sekar Kathiresan Muredach P Reilly Gudmar Thorleifsson Benjamin F Voight Jeanette Erdmann Christina Willenborg Dhananjay Vaidya Changchun Xie Chris C Patterson Thomas M Morgan Mary Susan Burnett Mingyao Li Mark A Hlatky Joshua W Knowles John R Thompson Devin Absher Carlos Iribarren Alan Go Stephen P Fortmann Stephen Sidney Neil Risch Hua Tang Richard M Myers Klaus Berger Monika Stoll Svati H Shah Gudmundur Thorgeirsson Karl Andersen Aki S Havulinna J Enrique Herrera Nauder Faraday Yoonhee Kim Brian G Kral Rasika A Mathias Ingo Ruczinski Bhoom Suktitipat Alexander F Wilson Lisa R Yanek Lewis C Becker Patrick Linsel-Nitschke Wolfgang Lieb Inke R König Christian Hengstenberg Marcus Fischer Klaus Stark Wibke Reinhard Janina Winogradow Martina Grassl Anika Grosshennig Michael Preuss Stefan Schreiber H-Erich Wichmann Christa Meisinger Jean Yee Yechiel Friedlander Ron Do James B Meigs Gordon Williams David M Nathan Calum A MacRae Liming Qu Robert L Wilensky William H Matthai Atif N Qasim Hakon Hakonarson Augusto D Pichard Kenneth M Kent Lowell Satler Joseph M Lindsay Ron Waksman Christopher W Knouff Dawn M Waterworth Max C Walker Vincent E Mooser Jaume Marrugat Gavin Lucas Isaac Subirana Joan Sala Rafael Ramos Nicola Martinelli Oliviero Olivieri Elisabetta Trabetti Giovanni Malerba Pier Franco Pignatti Candace Guiducci Daniel Mirel Melissa Parkin Joel N Hirschhorn Rosanna Asselta Stefano Duga Kiran Musunuru Mark J Daly Shaun Purcell Sandra Eifert Peter S Braund Benjamin J Wright Anthony J Balmforth Stephen G Ball Willem H Ouwehand Panos Deloukas Michael Scholz Francois Cambien Andreas Huge Thomas Scheffold Veikko Salomaa Domenico Girelli Christopher B Granger Leena Peltonen Pascal P McKeown David Altshuler Olle Melander Joseph M Devaney Stephen E Epstein Daniel J Rader Roberto Elosua James C Engert Sonia S Anand Alistair S Hall Andreas Ziegler Christopher J O'Donnell John A Spertus David Siscovick Stephen M Schwartz Diane Becker Unnur Thorsteinsdottir Kari Stefansson Heribert Schunkert Nilesh J Samani Thomas Quertermous

J Am Coll Cardiol 2010 Nov;56(19):1552-63

Department of Medicine, Stanford University School of Medicine, Stanford, California 94304-1334, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jacc.2010.06.022DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084526PMC
November 2010

Identification of susceptibility loci for scoliosis in FIS families with triple curves.

Am J Med Genet A 2010 Apr;152A(4):846-55

Department of Orthopaedic Surgery, Institute of Genetic Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.33222DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3392017PMC
April 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.

View Article

Download full-text PDF

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

Heritability of quantitative traits associated with type 2 diabetes mellitus in large multiplex families from South India.

Metabolism 2009 Oct 1;58(10):1439-45. Epub 2009 Jul 1.

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

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.metabol.2009.04.041DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3408214PMC
October 2009

A novel variant in the platelet endothelial aggregation receptor-1 gene is associated with increased platelet aggregability.

Arterioscler Thromb Vasc Biol 2008 Aug 29;28(8):1484-90. Epub 2008 May 29.

Departments of Medicine and Anesthesiology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287, USA.

View Article

Download full-text PDF

Source
https://www.ahajournals.org/doi/10.1161/ATVBAHA.108.168971
Publisher Site
http://dx.doi.org/10.1161/ATVBAHA.108.168971DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2739240PMC
August 2008

Association of GRIK4 with outcome of antidepressant treatment in the STAR*D cohort.

Am J Psychiatry 2007 Aug;164(8):1181-8

Genetic Basis of Mood and Anxiety Disorders, Mood and Anxiety Program, NIMH, NIH, Department of Health and Human Services, Bethesda, MD, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1176/appi.ajp.2007.06111790DOI Listing
August 2007

Association between a functional serotonin transporter promoter polymorphism and citalopram treatment in adult outpatients with major depression.

Arch Gen Psychiatry 2007 Jul;64(7):783-92

Section on Molecular Genetics, Laboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD 20892, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/archpsyc.64.7.783DOI Listing
July 2007

Heritability of platelet responsiveness to aspirin in activation pathways directly and indirectly related to cyclooxygenase-1.

Circulation 2007 May 30;115(19):2490-6. Epub 2007 Apr 30.

Department of Anesthesiology/Critical Care Medicine, Division of Cardiac Surgical Intensive Care, Johns Hopkins Medical Institutions, Baltimore, MD, USA.

View Article

Download full-text PDF

Source
https://www.ahajournals.org/doi/10.1161/CIRCULATIONAHA.106.6
Publisher Site
http://dx.doi.org/10.1161/CIRCULATIONAHA.106.667584DOI Listing
May 2007

Segregation analysis of restless legs syndrome: possible evidence for a major gene in a family study using blinded diagnoses.

Hum Hered 2006 24;62(3):157-64. Epub 2006 Oct 24.

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

View Article

Download full-text PDF

Source
https://www.karger.com/Article/FullText/96443
Publisher Site
http://dx.doi.org/10.1159/000096443DOI Listing
February 2007

Idiopathic scoliosis: identification of candidate regions on chromosome 19p13.

Spine (Phila Pa 1976) 2006 Jul;31(16):1815-9

Department of Orthopaedic Surgery, Johns Hopkins University, Baltimore, MD, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/01.brs.0000227264.23603.dcDOI Listing
July 2006

Lack of association between the aggrecan gene and familial idiopathic scoliosis.

Spine (Phila Pa 1976) 2006 Jun;31(13):1420-5

Johns Hopkins University, Baltimore, MD, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/01.brs.0000219944.18223.52DOI Listing
June 2006

Linkage analysis of genetic loci for kyphoscoliosis on chromosomes 5p13, 13q13.3, and 13q32.

Am J Med Genet A 2006 May;140(10):1059-68

Department of Orthopaedic Surgery, Institute of Genetic Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21287, USA.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/ajmg.a.31211
Publisher Site
http://dx.doi.org/10.1002/ajmg.a.31211DOI Listing
May 2006

Variation in the gene encoding the serotonin 2A receptor is associated with outcome of antidepressant treatment.

Am J Hum Genet 2006 May 20;78(5):804-814. Epub 2006 Mar 20.

Laboratory of Molecular Pathophysiology, Mood and Anxiety Program, National Institute of Mental Health (NIMH), National Institutes of Health (NIH), Department of Health and Human Services (DHHS), Bethesda.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1086/503820DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1474035PMC
May 2006

Allele frequency misspecification: effect on power and Type I error of model-dependent linkage analysis of quantitative traits under random ascertainment.

BMC Genet 2006 Apr 20;7:21. Epub 2006 Apr 20.

Department of Genetics, Louisiana State University Health Sciences Center, CSRB 6-16, New Orleans, LA 70112, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/1471-2156-7-21DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1475629PMC
April 2006

Critical values and variation in type I error along chromosomes in the COGA dataset using the applied pseudo-trait method.

BMC Genet 2005 Dec 30;6 Suppl 1:S54. Epub 2005 Dec 30.

Genometrics Section, Inherited Disease Research Branch, NHGRI/NIH, Baltimore, MD, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/1471-2156-6-S1-S54DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866729PMC
December 2005

Application of the regression of offspring on mid-parent method to detect associations between single-nucleotide polymorphisms and the beta 2 electroencephalogram phenotype in the COGA data.

BMC Genet 2005 Dec 30;6 Suppl 1:S56. Epub 2005 Dec 30.

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

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/1471-2156-6-S1-S56DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866727PMC
December 2005

Quantitative genetic analysis of blood pressure response during the cold pressor test.

Am J Hypertens 2005 Sep;18(9 Pt 1):1211-7

Lifespan Health Research Center, Wright State University School of Medicine, 3171 Research Boulevard, Dayton, OH 45420, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.amjhyper.2004.11.041DOI Listing
September 2005

Genetics of ultrasonographic carotid atherosclerosis.

Arterioscler Thromb Vasc Biol 2004 Sep 15;24(9):1567-77. Epub 2004 Jul 15.

Division of Epidemiology and Clinical Applications, National Heart, Lung, and Blood Institute, 6701 Rockledge Drive, MSC 7934, Bethesda, MD 20892-7934, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1161/01.ATV.0000138789.11433.c1DOI Listing
September 2004

Comparison of year-of-exam- and age-matched estimates of heritability in the Framingham Heart Study data.

BMC Genet 2003 Dec 31;4 Suppl 1:S36. Epub 2003 Dec 31.

Genometrics Section, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Drive, Baltimore, Maryland, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/1471-2156-4-S1-S36DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866471PMC
December 2003

Sex differences in heritability of sensitization to Blomia tropicalis in asthma using regression of offspring on midparent (ROMP) methods.

Hum Genet 2003 Oct 20;113(5):437-46. Epub 2003 Aug 20.

Division of Epidemiology and Clinical Applications, National Heart, Lung,and Blood Institute, 6701 Rockledge Drive, Rm. 8160, Bethesda, MD 20892-7934, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00439-003-1005-6DOI Listing
October 2003

A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21.

Hum Genet 2003 Jul 3;113(1):1-9. Epub 2003 Apr 3.

McKusick-Nathans Institute of Genetic Medicine, Center for Craniofacial Development and Disorders, Department of Pediatrics, The Johns Hopkins University School of Medicine, MD 21287-3914, Baltimore, USA.

View Article

Download full-text PDF

Source
http://link.springer.com/content/pdf/10.1007/s00439-003-0932
Web Search
http://link.springer.de/link/service/journals/00439/contents
Publisher Site
http://dx.doi.org/10.1007/s00439-003-0932-6DOI Listing
July 2003

Correlates of sensitization to Blomia tropicalis and Dermatophagoides pteronyssinus in asthma in Barbados.

Int Arch Allergy Immunol 2003 Jun;131(2):119-26

Division of Epidemiology and Clinical Applications, National Heart, Lung, and Blood Institute, Bethesda, MD 20892-7934, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000070927DOI Listing
June 2003

Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus.

Spine (Phila Pa 1976) 2003 Mar;28(6):589-94

Genometrics Section, NHGRI, National Institutes of Health, Baltimore, Maryland, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/01.BRS.0000049940.39801.E6DOI Listing
March 2003

An evaluation of the variance components approach: type I error, power and size of the estimated effect.

Eur J Hum Genet 2002 Feb;10(2):133-6

Department of Epidemiology, School of Public Health, Johns Hopkins University, Baltimore, MD, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/sj.ejhg.5200772DOI Listing
February 2002