Works matching AU Simpson, Claire L.

Results: 25

Regression and data mining methods for analyses of multiple rare variants in the Genetic Analysis Workshop 17 mini-exome data.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S92, doi. 10.1002/gepi.20657

By:

Bailey-Wilson, Joan E.;
Brennan, Jennifer S.;
Bull, Shelley B.;
Culverhouse, Robert;
Kim, Yoonhee;
Jiang, Yuan;
Jung, Jeesun;
Li, Qing;
Lamina, Claudia;
Liu, Ying;
Mägi, Reedik;
Niu, Yue S.;
Simpson, Claire L.;
Wang, Libo;
Yilmaz, Yildiz E.;
Zhang, Heping;
Zhang, Zhaogong

Publication type:

Article

Practical Barriers and Ethical Challenges in Genetic Data Sharing.

Published in:

International Journal of Environmental Research & Public Health, 2014, v. 11, n. 8, p. 8383, doi. 10.3390/ijerph110808383

By:

Simpson, Claire L.;
Goldenberg, Aaron J.;
Culverhouse, Rob;
Daley, Denise;
Igo Jr., Robert P.;
Jarvik, Gail P.;
Mandal, Diptasri M.;
Mascalzoni, Deborah;
Montgomery, Courtney Gray;
Pierce, Brandon L.;
Plaetke, Rosemarie;
Shete, Sanjay;
Goddard, Katrina A. B.;
Stein, Catherine M.

Publication type:

Article

The genetic dissection of Myo7a gene expression in the retinas of BXD mice.

Published in:

Molecular Vision, 2018, v. 24, p. 115

By:

Ye Lu;
Zhou, Diana;
King, Rebecca;
Shuang Zhu;
Simpson, Claire L.;
Jones, Byron C.;
Wenbo Zhang;
Geisert, Eldon E.;
Lu Lu

Publication type:

Article

Myopia in Chinese families shows linkage to 10q26.13.

Published in:

Molecular Vision, 2018, v. 24, p. 29

By:

Musolf, Anthony M.;
Simpson, Claire L.;
Long, Kyle A.;
Moiz, Bilal A.;
Lewis, Deyana D.;
Middlebrooks, Candace D.;
Portas, Laura;
Murgia, Federico;
Ciner, Elise B.;
Bailey-Wilson, Joan E.;
Stambolian, Dwight

Publication type:

Article

A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays.

Published in:

Nucleic Acids Research, 2005, v. 33, n. 3, p. e25, doi. 10.1093/nar/gni028

By:

Simpson, Claire L.;
Knight, Joanne;
Butcher, Lee M.;
Hansen, Valerie K.;
Meaburn, Emma;
Schalkwyk, Leonard C.;
Craig, Ian W.;
Powell, John F.;
Sham, Pak C.;
Al-Chalabi, Ammar

Publication type:

Article

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

Published in:

European Journal of Human Genetics, 2013, v. 21, n. 4, p. 437, doi. 10.1038/ejhg.2012.185

By:

Simpson, Claire L;
Cropp, Cheryl D;
Wahlfors, Tiina;
George, Asha;
Jones, MaryPat S;
Harper, Ursula;
Ponciano-Jackson, Damaris;
Tammela, Teuvo;
Schleutker, Johanna;
Bailey-Wilson, Joan E

Publication type:

Article

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.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S83

By:

Simpson, Claire L.;
Justice, Cristina M.;
Krishnan, Mera;
Wojciechowski, Robert;
Heejong Sung;
Cai, Jerry;
Green, Tiffany;
Lewis, Deyana;
Behneman, Dana;
Wilson, Alexander F.;
Bailey-Wilson, Joan E.

Publication type:

Article

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

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S15

By:

Heejong Sung;
Yoonhee Kim;
Juanliang Cai;
Cropp, Cheryl D.;
Simpson, Claire L.;
Qing Li;
Perry, Brian C.;
Sorant, Alexa J. M.;
Bailey-Wilson, Joan E.;
Wilson, Alexander F.

Publication type:

Article

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

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S104

By:

Yoonhee Kim;
Qing Li;
Cropp, Cheryl D.;
Heejong Sung;
Juanliang Cai;
Simpson, Claire L.;
Perry, Brian;
Dasgupta, Abhijit;
Malley, James D.;
Wilson, Alexander F.;
Bailey-Wilson, Joan E.

Publication type:

Article

Parametric Linkage Analysis Identifies Five Novel Genome-Wide Significant Loci for Familial Lung Cancer.

Published in:

Human Heredity, 2017, v. 82, n. 1/2, p. 64, doi. 10.1159/000479028

By:

Musolf, Anthony M.;
Simpson, Claire L.;
de Andrade, Mariza;
Mandal, Diptasri;
Gaba, Colette;
Ping Yang;
Yafang Li;
Ming You;
Kupert, Elena Y.;
Anderson, Marshall W.;
Schwartz, Ann G.;
Pinney, Susan M.;
Amos, Christopher I.;
Bailey-Wilson, Joan E.

Publication type:

Article

Trans-ancestry, Bayesian meta-analysis discovers 20 novel risk loci for inflammatory bowel disease in an African American, East Asian and European cohort.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 5, p. 873, doi. 10.1093/hmg/ddac269

By:

Cordero, Roberto Y;
Cordero, Jennifer B;
Stiemke, Andrew B;
Datta, Lisa W;
Buyske, Steven;
Kugathasan, Subra;
McGovern, Dermot P B;
Brant, Steven R;
Simpson, Claire L

Publication type:

Article

Familial Lung Cancer: A Brief History from the Earliest Work to the Most Recent Studies.

Published in:

Genes, 2017, v. 8, n. 1, p. 36, doi. 10.3390/genes8010036

By:

Musolf, Anthony M.;
Simpson, Claire L.;
de Andrade, Mariza;
Mandal, Diptasri;
Gaba, Colette;
Ping Yang;
Yafang Li;
Ming You;
Kupert, Elena Y.;
Anderson, Marshall W.;
Schwartz, Ann G.;
Pinney, Susan M.;
Amos, Christopher I.;
Bailey-Wilson, Joan E.

Publication type:

Article

Fetal High-Risk APOL1 Genotype Increases Risk for Small for Gestational Age in Term Infants Affected by Preeclampsia.

Published in:

Neonatology (16617800), 2023, v. 120, n. 4, p. 532, doi. 10.1159/000529850

By:

Azhibekov, Timur;
Durodoye, Razaq;
Miller, Anna K.;
Simpson, Claire L.;
Davis, Robert L.;
Williams, Scott M.;
Bruggeman, Leslie A.

Publication type:

Article

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

Published in:

Nature Genetics, 2013, v. 45, n. 6, p. 712, doi. 10.1038/ng0613-712b

By:

Verhoeven, Virginie J M;
Hysi, Pirro G;
Wojciechowski, Robert;
Fan, Qiao;
Guggenheim, Jeremy A;
Höhn, René;
MacGregor, Stuart;
Hewitt, Alex W;
Nag, Abhishek;
Cheng, Ching-Yu;
Yonova-Doing, Ekaterina;
Zhou, Xin;
Ikram, M Kamran;
Buitendijk, Gabriëlle H S;
McMahon, George;
Kemp, John P;
Pourcain, Beate St;
Simpson, Claire L;
Mäkelä, Kari-Matti;
Lehtimäki, Terho

Publication type:

Article

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

Published in:

Nature Genetics, 2013, v. 45, n. 3, p. 314, doi. 10.1038/ng.2554

By:

Verhoeven, Virginie J M;
Hysi, Pirro G;
Wojciechowski, Robert;
Fan, Qiao;
Guggenheim, Jeremy A;
Höhn, René;
MacGregor, Stuart;
Hewitt, Alex W;
Nag, Abhishek;
Cheng, Ching-Yu;
Yonova-Doing, Ekaterina;
Zhou, Xin;
Ikram, M Kamran;
Buitendijk, Gabriëlle H S;
McMahon, George;
Kemp, John P;
Pourcain, Beate St;
Simpson, Claire L;
Mäkelä, Kari-Matti;
Lehtimäki, Terho

Publication type:

Article

Genome-wide linkage scan for prostate cancer susceptibility in Finland: Evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22.

Published in:

International Journal of Cancer, 2011, v. 129, n. 10, p. 2400, doi. 10.1002/ijc.25906

By:

Cropp, Cheryl D.;
Simpson, Claire L;
Wahlfors, Tiina;
Ha, Nati;
George, Asha;
Jones, MaryPat S.;
Harper, Ursula;
Ponciano-Jackson, Damaris;
Green, Tiffany A.;
Tammela, Teuvo L. J.;
Bailey-Wilson, Joan;
Schleutker, Johanna

Publication type:

Article

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

Published in:

Human Genetics, 2019, v. 138, n. 4, p. 339, doi. 10.1007/s00439-019-01991-0

By:

Musolf, Anthony M.;
Simpson, Claire L.;
Alexander, Theresa A.;
Portas, Laura;
Murgia, Federico;
Ciner, Elise B.;
Stambolian, Dwight;
Bailey-Wilson, Joan E.

Publication type:

Article

Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world.

Published in:

Frontiers in Genetics, 2015, p. 1, doi. 10.3389/fgene.2015.00238

By:

Morrison, Margaux A.;
Magalhaes, Tiago R.;
Ramke, Jacqueline;
Smith, Silvia E.;
Ennis, Sean;
Simpson, Claire L.;
Murgia, Federico;
Ahn, Jeeyun;
Dardenne, Caitlin;
Mayne, Katie;
Robinson, Rosann;
Morgan, Denise J.;
Brian, Garry;
Lucy Lee;
Woo, Se J.;
Zacharaki, Fani;
Tsironi, Evangelia E.;
Miller, Joan W.;
Kim, Ivana K.;
Park, Kyu H.

Publication type:

Article

Effect of statin treatment on metabolites, lipids and prostanoids in patients with Statin Associated Muscle Symptoms (SAMS).

Published in:

PLoS ONE, 2023, v. 18, n. 12, p. 1, doi. 10.1371/journal.pone.0294498

By:

Garrett, Timothy J.;
Puchowicz, Michelle A.;
Park, Edwards A.;
Dong, Qingming;
Farage, Gregory;
Childress, Richard;
Guingab, Joy;
Simpson, Claire L.;
Sen, Saunak;
Brogdon, Elizabeth C.;
Buchanan, Logan M.;
Raghow, Rajendra;
Elam, Marshall B.

Publication type:

Article

Large-scale pathways-based association study in amyotrophic lateral sclerosis.

Published in:

Brain: A Journal of Neurology, 2007, v. 130, n. 9, p. 2292

By:

Dalia Kasperaviciute;
Mike E. Weale;
Kevin V. Shianna;
Gareth T. Banks;
Claire L. Simpson;
Valerie K. Hansen;
Martin R. Turner;
Christopher E. Shaw;
Ammar Al-Chalabi;
Hardev S. Pall;
Emily F. Goodall;
Karen E. Morrison;
Richard W. Orrell;
Marcus Beck;
Sibylle Jablonka;
Michael Sendtner;
Alice Brockington;
Paul G. Ince;
Judith Hartley;
Hannah Nixon

Publication type:

Article

Genome-Wide Meta-Analysis of Myopia and Hyperopia Provides Evidence for Replication of 11 Loci.

Published in:

PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0107110

By:

Simpson, Claire L.;
Wojciechowski, Robert;
Oexle, Konrad;
Murgia, Federico;
Portas, Laura;
Li, Xiaohui;
Verhoeven, Virginie J. M.;
Vitart, Veronique;
Schache, Maria;
Hosseini, S. Mohsen;
Hysi, Pirro G.;
Raffel, Leslie J.;
Cotch, Mary Frances;
Chew, Emily;
Klein, Barbara E. K.;
Klein, Ronald;
Wong, Tien Yin;
van Duijn, Cornelia M.;
Mitchell, Paul;
Saw, Seang Mei

Publication type:

Article

Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0752-8

By:

Simpson, Claire L.;
Musolf, Anthony M.;
Li, Qing;
Portas, Laura;
Murgia, Federico;
Cordero, Roberto Y.;
Cordero, Jennifer B.;
Moiz, Bilal A.;
Holzinger, Emily R.;
Middlebrooks, Candace D.;
Lewis, Deyana D.;
Bailey-Wilson, Joan E.;
Stambolian, Dwight

Publication type:

Article

A novel de novo TP63 mutation in whole‐exome sequencing of a Syrian family with Oral cleft and ectrodactyly.

Published in:

Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 8, p. 1, doi. 10.1002/mgg3.2179

By:

Simpson, Claire L.;
Kimble, Danielle C.;
Chandrasekharappa, Settara C.;
Alqosayer, Khalid;
Holzinger, Emily;
Carrington, Blake;
McElderry, John;
Sood, Raman;
Al‐Souqi, Ghiath;
Albacha‐Hejazi, Hasan;
Bailey‐Wilson, Joan E.

Publication type:

Article

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 13, p. 2754

By:

Stambolian, Dwight;
Wojciechowski, Robert;
Oexle, Konrad;
Pirastu, Mario;
Li, Xiaohui;
Raffel, Leslie J.;
Cotch, Mary Frances;
Chew, Emily Y.;
Klein, Barbara;
Klein, Ronald;
Wong, Tien Y.;
Simpson, Claire L.;
Klaver, Caroline C.W.;
van Duijn, Cornelia M.;
Verhoeven, Virginie J.M.;
Baird, Paul N.;
Vitart, Veronique;
Paterson, Andrew D.;
Mitchell, Paul;
Saw, Seang Mei

Publication type:

Article

Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 3, p. 472, doi. 10.1093/hmg/ddn375

By:

Simpson, Claire L.;
Lemmens, Robin;
Miskiewicz, Katarzyna;
Broom, Wendy J.;
Hansen, Valerie K.;
van Vught, Paul W.J.;
Landers, John E.;
Sapp, Peter;
Van Den Bosch, Ludo;
Knight, Joanne;
Neale, Benjamin M.;
Turner, Martin R.;
Veldink, Jan H.;
Ophoff, Roel A.;
Tripathi, Vineeta B.;
Beleza, Ana;
Shah, Meera N.;
Proitsi, Petroula;
Van Hoecke, Annelies;
Carmeliet, Peter

Publication type:

Article