Baylor Genetics

InstitutionResearch output, impact & collaborations

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.

4,640

Works

3,334,082

Citations

865

Researchers

Avg h-index

IDs:ROR OpenAlex

How has Baylor Genetics's publication output changed over time?

ScholarIQpublication output · 2006–2019

Output grew0% over the shown period — from 1 works in 2006 to 1 in 2019.

2006200820182019

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

S42433034. 2018651 CitationsOPEN ACCESS

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

S2737523697. 2019282 CitationsOPEN ACCESS

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

S187186932. 2006271 CitationsOPEN ACCESS

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

S171405753. 2008266 Citations