ScholarIQanswers from OpenAlex & ORCID
Christine M. Eng
ResearcherPublications, citations & collaboration network
Christine M. Eng is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Christine M. Eng have?
ScholarIQindexed works
Christine M. Eng has 274 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Christine M. Eng have?
ScholarIQcitation count
Christine M. Eng has 24,465 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Christine M. Eng?
ScholarIQh-index
Christine M. Eng has an h-index of 70 in OpenAlex.
What is the i10-index of Christine M. Eng?
ScholarIQi10-index
Christine M. Eng has an i10-index of 167 in OpenAlex.
What is the ORCID of Christine M. Eng?
ScholarIQorcid
The ORCID for Christine M. Eng is on the source record.
What is the OpenAlex record for Christine M. Eng?
ScholarIQopenalex
The OpenAlex for Christine M. Eng is on the source record.
What are the most-cited papers on Christine M. Eng?
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
Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between
Gail P. Jarvik, Laura M. Amendola, Jonathan S. Berg, Kyle B. Brothers, Ellen Wright Clayton, Wendy K. Chung, Barbara J. Evans, James P. Evans, Stephanie M. Fullerton, Carlos J. Gallego, Nanibaa’ A. Garrison, Stacy W. Gray, Ingrid A. Holm, Iftikhar J. Kullo, Lisa Soleymani Lehmann, Cathy McCarty, Cynthia A. Prows, Heidi L. Rehm, Richard R. Sharp, Joseph K. Salama, Saskia C. Sanderson, Sara L. Van Driest, Marc S. Williams, Susan M. Wolf, Wendy A. Wolf, Wylie Burke, John B. Harley, Melanie F. Myers, Bahram Namjou, Sander Vinks, John J. Connolly, Brendan J. Keating, Glenn S. Gerhard, Agnes S. Sundaresan, Gerard Tromp, David R. Crosslin, Kathy Leppig, Cathy Wicklund, Christopher G. Chute, John Lynch, Mariza de Andrade, John A. Heit, Jen McCormick, Murray H. Brilliant, Terrie Kitchner, Marylyn D. Ritchie, Erwin P. Böttinger, Inga Peter, Stephen D. Persell, Laura J. Rasmussen‐Torvik, Tracy L. McGregor, Dan M. Roden, Armand H. Matheny Antommaria, Rosetta Chiavacci, Andy Faucett, David H. Ledbetter, Janet L. Williams, Andrea L. Hartzler, Carolyn R. Rohrer Vitek, Norm Frost, Kadija Ferryman, Carol R. Horowitz, Rosamond Rhodes, Randi E. Zinberg, Sharon Aufox, Vivian Pan, Rochelle M. Long, Erin M. Ramos, Jackie Odgis, Anastasia L. Wise, Sara Chandros Hull, Jonathan D. Gitlin, Robert C. Green, Danielle R. Metterville, Amy L. McGuire, Sek Won Kong, Sue Trinidad, David L. Veenstra, Myra I. Roche, Debra Skinner, Kelly Raspberry, Julianne O’Daniel, William H. Parsons, Christine M. Eng, Susan G. Hilsenbeck, Dean Karavite, Laura K. Conlin, Nancy B. Spinner, Ian D. Krantz, Marni J. Falk, Avni Santani, Elizabeth T. DeChene, Matthew C. Dulik, Barbara A. Bernhardt, Scott M. Schuetze, Jessica N. Everett, Michele C. Gornick, Ben Wilfond, Holly K. Tabor, Amy A. Lemke
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