ScholarIQanswers from OpenAlex
Baylor Genetics
InstitutionResearch output, impact & collaborations
Baylor Genetics is a institution indexed in ScholarIQ from OpenAlex.
What is known about Baylor Genetics?
ScholarIQrecord summary
Baylor Genetics is a research organisation in Houston, US. OpenAlex records 4,640 works and 3,334,082 citations for it. 865 researchers list it as their most recent affiliation.
How many works does Baylor Genetics have?
ScholarIQindexed works
Baylor Genetics has 4,640 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Baylor Genetics have?
ScholarIQcitation count
Baylor Genetics has 3,334,082 citations in the OpenAlex counts ScholarIQ stores.
How many researchers are at Baylor Genetics?
ScholarIQresearcher count
Baylor Genetics has 865 researchers in the ScholarIQ index.
What is the average h-index at Baylor Genetics?
ScholarIQavg h-index
Baylor Genetics has an average h-index of 70 in OpenAlex.
What is the ROR of Baylor Genetics?
ScholarIQror
The ROR for Baylor Genetics is on the source record.
What is the OpenAlex record for Baylor Genetics?
ScholarIQopenalex
The OpenAlex for Baylor Genetics is on the source record.
Who are the most-cited researchers behind Baylor Genetics?
ScholarIQtop researchers by citations
What are the most-cited papers on Baylor Genetics?
ScholarIQmost cited works
Fabry disease revisited: Management and treatment recommendations for adult patients
Alberto Ortíz, Dominique P. Germain, Robert J. Desnick, Juan Politei, Michael Mauer, Alessandro P. Burlina, Christine M. Eng, Robert J. Hopkin, Dawn A. Laney, Aleš Linhart, Stephen Waldek, Eric Wallace, Frank Weidemann, William R. Wilcox
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes
Pamela Feliciano, Xueya Zhou, Irina Astrovskaya, Tychele N. Turner, Tianyun Wang, Leo Brueggeman, Rebecca Barnard, Alexander Hsieh, LeeAnne Green Snyder, Donna M. Muzny, Aniko Sabo, Leonard Abbeduto, John Acampado, Andrea J. Ace, Charles F. Albright, Michael Alessandri, David G. Amaral, Alpha Amatya, Robert D. Annett, Ivette Arriaga, Ethan Bahl, Adithya Balasubramanian, Nicole Bardett, Asif Bashar, Arthur L. Beaudet, Landon Beeson, Raphael Bernier, Elizabeth Berry‐Kravis, Stephanie Booker, Stephanie Brewster, Elizabeth Brooks, Martin E. Butler, Eric Butter, Kristen Callahan, Alexies Camba, Sarah Carpenter, Nicholas Carriero, Lindsey A. Cartner, Ahmad S. Chatha, Wubin Chin, Renee D. Clark, Cheryl Cohen, Eric Courchesne, Joseph F. Cubells, Mary Hannah Currin, Amy M. Daniels, Lindsey DeMarco, Megan Y. Dennis, Gabriel S. Dichter, Yan Ding, Huyen Dinh, Ryan N. Doan, HarshaVardhan Doddapaneni, Sara Eldred, Christine M. Eng, Craig A. Erickson, Amy Esler, Ali Fatemi, Gregory J. Fischer, I. Fisk, Éric Fombonne, Emily A. Fox, Sunday M. Francis, Sandra Friedman, Swami Ganesan, Michael R. Garrett, Vahid Gazestani, Madeleine R. Geisheker, Jennifer Gerdts, Daniel H. Geschwind, Robin P. Goin‐Kochel, Anthony J. Griswold, Luke P. Grosvenor, Angela Gruber, Amanda C. Gulsrud, Jaclyn Gunderson, Anibal Gutierrez, Melissa N. Hale, Monica Haley, Jacob B. Hall, Kira E. Hamer, Bing Han, Nathan Hanna, Christina Harkins, Nina Harris, Brenda Hauf, Caitlin Hayes, Susan Hepburn, Lynette M. Herbert, Michelle Heyman, Brittani A. Phillips, Susannah Horner, Taobo Hu, Lark Y. Huang-Storms, Hanna Hutter, Dalia Istephanous, Suma Jacob, William B. Jensen, Mark Jones, Michelle Jordy
Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males
Daniela del Gaudio, Ping Fang, Fernando Scaglia, Patricia A. Ward, William J. Craigen, Daniel G. Glaze, Jeffrey L. Neul, Ankita Patel, Jennifer A. Lee, Mira Irons, Susan A. Berry, Amber A. Pursley, Theresa A. Grebe, Debra Freedenberg, Rick A. Martin, Gary Hsich, Jena R Khera, Neil Friedman, Huda Y. Zoghbi, Christine M. Eng, James R. Lupski, Arthur L. Beaudet, Sau Wai Cheung, Benjamin B. Roa
Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases
Ignatia B. Van den Veyver, Ankita Patel, Chad A. Shaw, Amber N. Pursley, Sung‐Hae Kang, Marcia J. Simovich, Patricia A. Ward, Sandra Darilek, Anthony E. Johnson, Sarah E. Neill, Weimin Bi, Lisa D. White, Christine M. Eng, James R. Lupski, Sau Wai Cheung, Arthur L. Beaudet
How much of the research on Baylor Genetics is open access?
ScholarIQopen access share
75%OPEN ACCESS