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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
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
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
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 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
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
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
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 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
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
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
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
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
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
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
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
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
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
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
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

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