ursaPGx: a new R package to annotate pharmacogenetic star alleles using phased whole-genome sequencing data von Calendo, Gennaro, Kusic, Dara, Madzo, Jozef, Gharani, Neda, Scheinfeldt, Laura

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Using the Coriell Personalized Medicine Collaborative Data to conduct a genome-wide association study of sleep duration von Scheinfeldt, Laura B., Gharani, Neda, Kasper, Rachel S., Schmidlen, Tara J., Gordon, Erynn S., Jarvis, Joseph P., Delaney, Susan, Kronenthal, Courtney J., Gerry, Norman P., Christman, Michael F.

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Genetic Knowledge Among Participants in the Coriell Personalized Medicine Collaborative von Schmidlen, Tara J., Scheinfeldt, Laura, Zhaoyang, Ruixue, Kasper, Rachel, Sweet, Kevin, Gordon, Erynn S., Keller, Margaret, Stack, Cathy, Gharani, Neda, Daly, Mary B., Jarvis, Joseph, Christman, Michael F.

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Remapping the Insulin Gene/IDDM2 Locus in Type 1 Diabetes von BARRATT, Bryan J, PAYNE, Felicity, MCCORMACK, Rose, GUJA, Cristian, IONESCU-URGOVIGTE, Constantin, UNDLIEN, Dag E, RØNNINGEN, Kjersti S, GILLESPIE, Kathleen M, TUOMILEHTO-WOLF, Eva, TUOMILEHTO, Jaakko, BENNETT, Simon T, CLAYTON, David G, LOWE, Chris E, CORDELL, Heather J, TODD, John A, HERMANN, Robert, HEALY, Barry C, HAROLD, Denise, CONCANNON, Patrick, GHARANI, Neda, MCCARTHY, Mark I, OLAVESEN, Mark G

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A global reference for human genetic variation von Auton, Adam, Brooks, Lisa D, Durbin, Richard M, Garrison, Erik P, Kang, Hyun Min, Korbel, Jan O, Marchini, Jonathan L, McCarthy, Shane, McVean, Gil A, Abecasis, Gonçalo R

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The variant call format and VCFtools von Danecek, Petr, Auton, Adam, Abecasis, Goncalo, Albers, Cornelis A., Banks, Eric, DePristo, Mark A., Handsaker, Robert E., Lunter, Gerton, Marth, Gabor T., Sherry, Stephen T., McVean, Gilean, Durbin, Richard

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Common Treatment, Common Variant: Evolutionary Prediction of Functional Pharmacogenomic Variants von Scheinfeldt, Laura B., Brangan, Andrew, Kusic, Dara M., Kumar, Sudhir, Gharani, Neda

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Autism-Associated Haplotype Affects the Regulation of the Homeobox Gene, ENGRAILED 2 von Benayed, Rym, Choi, Jiyeon, Matteson, Paul G, Gharani, Neda, Kamdar, Silky, Brzustowicz, Linda M, Millonig, James H

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An expanded pharmacogenomics warfarin dosing table with utility in generalised dosing guidance von Shahabi, Payman, Scheinfeldt, Laura B., Lynch, Daniel E., Schmidlen, Tara J., Perreault, Sylvie, Keller, Margaret A., Kasper, Rachel, Wawak, Lisa, Jarvis, Joseph P., Gerry, Norman P., Gordon, Erynn S., Christman, Michael F., Dubé, Marie-Pierre, Gharani, Neda

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Support for the Homeobox Transcription Factor Gene ENGRAILED 2 as an Autism Spectrum Disorder Susceptibility Locus von Benayed, Rym, Gharani, Neda, Rossman, Ian, Mancuso, Vincent, Lazar, Gloria, Kamdar, Silky, Bruse, Shannon E., Tischfield, Samuel, Smith, Brett J., Zimmerman, Raymond A., DiCicco-Bloom, Emanuel, Brzustowicz, Linda M., Millonig, James H.

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Genetic risk estimation in the Coriell Personalized Medicine Collaborative von Stack, Catharine B., Gharani, Neda, Gordon, Erynn S., Schmidlen, Tara, Christman, Michael F., Keller, Margaret A.

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The Coriell personalized medicine collaborative pharmacogenomics appraisal, evidence scoring and interpretation system von Gharani, Neda, Keller, Margaret A, Stack, Catharine B, Hodges, Laura M, Schmidlen, Tara J, Lynch, Daniel E, Gordon, Erynn S, Christman, Michael F

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The genetic basis of polycystic ovary syndrome von Franks, S, Gharani, N, Waterworth, D, Batty, S, White, D, Williamson, R, McCarthy, M

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Association of the Steroid Synthesis Gene Cyp11a with Polycystic Ovary Syndrome and Hyperandrogenism von Gharani, Neda, Waterworth, Dawn M., Batty, Sari, White, Davinia, Gilling-Smith, Carole, Conway, Gerard S., McCarthy, Mark, Franks, Stephen, Williamson, Robert

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Large-Scale Analysis of the Relationship between CYP11A Promoter Variation, Polycystic Ovarian Syndrome, and Serum Testosterone von Gaasenbeek, Michelle, Powell, Brenda L., Sovio, Ulla, Haddad, Lema, Gharani, Neda, Bennett, Amanda, Groves, Christopher J., Rush, Karen, Goh, Micaela J., Conway, Gerard S., Ruokonen, Aimo, Martikainen, Hannu, Pouta, Anneli, Taponen, Saara, Hartikainen, Anna-Liisa, Halford, Stephanie, Järvelin, Marjo-Riitta, Franks, Steve, McCarthy, Mark I.

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Common genetic risk for melanoma encourages preventive behavior change von Diseati, Lori, Scheinfeldt, Laura B, Kasper, Rachel S, Zhaoyang, Ruixue, Gharani, Neda, Schmidlen, Tara J, Gordon, Erynn S, Sessions, Cecili K, Delaney, Susan K, Jarvis, Joseph P, Gerry, Norman, Christman, Michael

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Linkage and association of insulin gene VNTR regulatory polymorphism with polycystic ovary syndrome von Waterworth, Dawn M, Bennett, Simon T, Gharani, Neda, McCarthy, Mark I, Hague, Stephen, Batty, Sari, Conway, Gerard S, White, Davinia, Todd, John A, Franks, Stephen, Williamson, Robert

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Three autism candidate genes: a synthesis of human genetic analysis with other disciplines von Bartlett, Christopher W., Gharani, Neda, Millonig, James H., Brzustowicz, Linda M.

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Analysis of Multiple Data Sets Reveals No Association between the Insulin Gene Variable Number Tandem Repeat Element and Polycystic Ovary Syndrome or Related Traits von Powell, Brenda L., Haddad, Lema, Bennett, Amanda, Gharani, Neda, Sovio, Ulla, Groves, Christopher J., Rush, Karen, Goh, Micaela J., Conway, Gerard S., Ruokonen, Aimo, Martikainen, Hannu, Pouta, Anneli, Taponen, Saara, Hartikainen, Anna-Liisa, Halford, Stephanie, Zeggini, Eleftheria, Järvelin, Marjo-Riitta, Franks, Steve, McCarthy, Mark I.

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Variation within the Type 2 Diabetes Susceptibility Gene Calpain-10 and Polycystic Ovary Syndrome von Haddad, Lema, Evans, Julie C., Gharani, Neda, Robertson, Carole, Rush, Karen, Wiltshire, Steven, Frayling, Timothy M., Wilkin, Terence J., Demaine, Andrew, Millward, Ann, Hattersley, Andrew T., Conway, Gerry, Cox, Nancy J., Bell, Graeme I., Franks, Steve, McCarthy, Mark I.

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