ScholarIQanswers from OpenAlex & ORCID
Heidi L. Rehm
ResearcherPublications, citations & collaboration network
Heidi L. Rehm is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Heidi L. Rehm have?
ScholarIQindexed works
Heidi L. Rehm has 525 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Heidi L. Rehm have?
ScholarIQcitation count
Heidi L. Rehm has 75,671 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Heidi L. Rehm?
ScholarIQh-index
Heidi L. Rehm has an h-index of 103 in OpenAlex.
What is the i10-index of Heidi L. Rehm?
ScholarIQi10-index
Heidi L. Rehm has an i10-index of 320 in OpenAlex.
What is the ORCID of Heidi L. Rehm?
ScholarIQorcid
The ORCID for Heidi L. Rehm is on the source record.
What is the OpenAlex record for Heidi L. Rehm?
ScholarIQopenalex
The OpenAlex for Heidi L. Rehm is on the source record.
What are the most-cited papers on Heidi L. Rehm?
ScholarIQmost cited works
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann, Sandrine Marlin, Françoise Denoyelle, J Waligora, Małgorzata Mueller‐Malesińska, Agneszka Pollak, Rafał Płoski, Alessandra Murgia, Eva Orzan, Pierangela Castorina, Umberto Ambrosetti, Ewa Nowakowska-Szyrwińska, Jerzy Bal, Wojciech Wiszniewski, Andreas Janecke, Doris Nekahm-Heis, Pavel Seeman, O. Bendová, Margaret A. Kenna, Anna Frangulov, Heidi L. Rehm, Mustafa Tekin, Armağan İncesulu, Hans‐Henrik M. Dahl, Desirée du Sart, Lucy Jenkins, Deirdre Lucas, Maria Bitner‐Glindzicz, Karen B. Avraham, Zippora Brownstein, Ignacio del Castillo, Felipe Moreno, Nikolaus Blin, Markus Pfister, István Sziklai, Tímea Tóth, Philip M. Kelley, Edward Cohn, Lionel Van Maldergem, Pascale Hilbert, Anne‐Françoise Roux, M. Mondain, Lies H. Hoefsloot, Cor W. R. J. Cremers, Tuija Löppönen, Heikki Löppönen, Agnete Parving, Karen Grønskov, Iris Schrijver, Joseph Roberson, Francesca Gualandi, Alessandro Martini, Geneviève Lina‐Granade, Nathalie Pallarès-Ruiz, Céu Correia, Graça Fialho, Kim Cryns, Nele Hilgert, Paul Van de Heyning, Carla Nishimura, Richard J. Smith, Guy Van Camp
International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases
Kym M. Boycott, Ana Rath, Jessica X. Chong, Taila Hartley, Fowzan S. Alkuraya, Gareth Baynam, Anthony J. Brookes, Michael Brudno, Ãngel Carracedo, Johan T. den Dunnen, Stephanie O. M. Dyke, Xavier Estivill, Jack Goldblatt, Catherine Gonthier, Stephen C. Groft, Marta Gut, Ada Hamosh, Philip Hieter, Sophie Höhn, Matthew E. Hurles, Petra Kaufmann, Bartha Maria Knoppers, Jeffrey P. Krischer, Milan Maçek, Gert Matthijs, Annie Olry, Samantha Parker, Justin Paschall, Anthony Philippakis, Heidi L. Rehm, Peter N. Robinson, Pak C. Sham, Румен Стефанов, Domenica Taruscio, Divya Unni, Megan R. Vanstone, Feng Zhang, Han G. Brunner, Michael J. Bamshad, Hanns Lochmüller
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing
Trevor J. Pugh, Melissa Kelly, Sivakumar Gowrisankar, Elizabeth Hynes, Michael A. Seidman, Samantha Baxter, Mark Bowser, Bryan D. Harrison, Daniel Aaron, Lisa Mahanta, Neal K. Lakdawala, Gregory C McDermott, Emily White, Heidi L. Rehm, Matthew S. Lebo, Birgit Funke
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
Insights into genetics, human biology and disease gleaned from family based genomic studies
Jennifer E. Posey, Anne O’Donnell‐Luria, Jessica X. Chong, Tamar Harel, Shalini N. Jhangiani, Zeynep H. Coban Akdemir, Steven Buyske, Davut Pehli̇van, Claudia M.B. Carvalho, Samantha Baxter, Nara Sobreira, Pengfei Liu, Nan Wu, Jill A. Rosenfeld, Sushant Kumar, Dimitri Avramopoulos, Janson J. White, Kimberly F. Doheny, P. Dane Witmer, Corinne D. Boehm, V. Reid Sutton, Donna M. Muzny, Eric Boerwinkle, Murat Günel, Deborah A. Nickerson, Shrikant Mane, Daniel G. MacArthur, Richard A. Gibbs, Ada Hamosh, Richard P. Lifton, Tara C. Matise, Heidi L. Rehm, Mark Gerstein, Michael J. Bamshad, David Valle, James R. Lupski