Curtis Rogers
Curtis C. Rogers Jr. is an American genetic genealogist, digital forensics specialist, and executive known for establishing GEDmatch, a genetic genealogy website. Provided by Wikipedia
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P163: Functional assessment of IGF-1 and hGH as candidate treatments for Phelan-McDermid syndrome* by Bridgette Moffitt, Jillian Spencer, Jennifer Benjock, Mary Kearns, Luigi Boccuto, Sara Sarasua, William Bennett, Diana Ivankovic, Katy Phelan, Curtis Rogers
Published 2024-01-01
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Head Size in Phelan–McDermid Syndrome: A Literature Review and Pooled Analysis of 198 Patients Identifies Candidate Genes on 22q13 by Sara M. Sarasua, Jane M. DeLuca, Curtis Rogers, Katy Phelan, Lior Rennert, Kara E. Powder, Katherine Weisensee, Luigi Boccuto
Published 2023-02-01
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Stratification of a Phelan–McDermid Syndrome Population Based on Their Response to Human Growth Hormone and Insulin-like Growth Factor by Bridgette A. Moffitt, Sara M. Sarasua, Diana Ivankovic, Linda D. Ward, Kathleen Valentine, William E. Bennett, Curtis Rogers, Katy Phelan, Luigi Boccuto
Published 2023-02-01
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Position effects of 22q13 rearrangements on candidate genes in Phelan-McDermid syndrome. by Sujata Srikanth, Lavanya Jain, Cinthya Zepeda-Mendoza, Lauren Cascio, Kelly Jones, Rini Pauly, Barb DuPont, Curtis Rogers, Sara Sarasua, Katy Phelan, Cynthia Morton, Luigi Boccuto
Published 2021-01-01
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RNA analysis of the GALNS transcript reveals novel pathogenic mechanisms associated with Morquio syndrome A by Young Bae Sohn, Curtis Rogers, Jennifer Stallworth, Jessica A. Cooley Coleman, Laura Buch, Erin Jozwiak, Jo Ann Johnson, Tim Wood, Paul Harmatz, Laura Pollard, Raymond J. Louie
Published 2022-06-01
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Phelan-McDermid syndrome: a classification system after 30 years of experience by Katy Phelan, Luigi Boccuto, Craig M. Powell, Tobias M. Boeckers, Conny van Ravenswaaij-Arts, R. Curtis Rogers, Carlo Sala, Chiara Verpelli, Audrey Thurm, William E. Bennett, Christopher J. Winrow, Sheldon R. Garrison, Roberto Toro, Thomas Bourgeron
Published 2022-01-01
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Gene domain-specific DNA methylation episignatures highlight distinct molecular entities of ADNP syndrome by Eric G. Bend, Erfan Aref-Eshghi, David B. Everman, R. Curtis Rogers, Sara S. Cathey, Eloise J. Prijoles, Michael J. Lyons, Heather Davis, Katie Clarkson, Karen W. Gripp, Dong Li, Elizabeth Bhoj, Elaine Zackai, Paul Mark, Hakon Hakonarson, Laurie A. Demmer, Michael A. Levy, Jennifer Kerkhof, Alan Stuart, David Rodenhiser, Michael J. Friez, Roger E. Stevenson, Charles E. Schwartz, Bekim Sadikovic
Published 2019-04-01
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KDM5A mutations identified in autism spectrum disorder using forward genetics by Lauretta El Hayek, Islam Oguz Tuncay, Nadine Nijem, Jamie Russell, Sara Ludwig, Kiran Kaur, Xiaohong Li, Priscilla Anderton, Miao Tang, Amanda Gerard, Anja Heinze, Pia Zacher, Hessa S Alsaif, Aboulfazl Rad, Kazem Hassanpour, Mohammad Reza Abbaszadegan, Camerun Washington, Barbara R DuPont, Raymond J Louie, CAUSES Study, Madeline Couse, Maha Faden, R Curtis Rogers, Rami Abou Jamra, Ellen R Elias, Reza Maroofian, Henry Houlden, Anna Lehman, Bruce Beutler, Maria H Chahrour
Published 2020-12-01
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