ScholarIQanswers from OpenAlex & ORCID
Deborah A. Nickerson
ResearcherPublications, citations & collaboration network
Deborah A. Nickerson is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Deborah A. Nickerson have?
ScholarIQindexed works
Deborah A. Nickerson has 653 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Deborah A. Nickerson have?
ScholarIQcitation count
Deborah A. Nickerson has 98,097 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Deborah A. Nickerson?
ScholarIQh-index
Deborah A. Nickerson has an h-index of 121 in OpenAlex.
What is the i10-index of Deborah A. Nickerson?
ScholarIQi10-index
Deborah A. Nickerson has an i10-index of 455 in OpenAlex.
What is the ORCID of Deborah A. Nickerson?
ScholarIQorcid
The ORCID for Deborah A. Nickerson is on the source record.
What is the OpenAlex record for Deborah A. Nickerson?
ScholarIQopenalex
The OpenAlex for Deborah A. Nickerson is on the source record.
What are the most-cited papers on Deborah A. Nickerson?
ScholarIQmost cited works
Somatic Mutations in Cerebral Cortical Malformations
Saumya Shekhar Jamuar, Anh-Thu N. Lam, Martin Kircher, Alissa M. D’Gama, Jian Wang, Brenda J. Barry, Xiaochang Zhang, Robert Hill, Jennifer N. Partlow, Aldo Rozzo, Sarah Servattalab, Bhaven K. Mehta, Meral Topçu, Dina Amrom, Eva Andermann, Bernard Dan, Elena Parrini, Renzo Guerrini, Ingrid E. Scheffer, Samuel F. Berkovic, Richard J. Leventer, Yiping Shen, Bai Lin Wu, A. James Barkovich, Mustafa Şahin, Bernard S. Chang, Michael J. Bamshad, Deborah A. Nickerson, Jay Shendure, Annapurna Poduri, Timothy W. Yu, Christopher A. Walsh
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data
Pierrick Wainschtein, Deepti Jain, Zhili Zheng, TOPMed Anthropometry Working Group, Stella Aslibekyan, Diane M. Becker, Wenjian Bi, Jennifer A. Brody, Jenna C. Carlson, Adolfo Correa, Margaret Mengmeng Du, Lindsay Fernández‐Rhodes, Kendra Ferrier, Misa Graff, Xiuqing Guo, Jiang He, Nancy L. Heard‐Costa, Heather M. Highland, Joel N. Hirschhorn, Candace M Howard-Claudio, Carmen R. Isasi, Rebecca D. Jackson, Jicai Jiang, Roby Joehanes, Anne E. Justice, Rita R. Kalyani, Sharon L. R. Kardia, Ethan M. Lange, Meryl S. LeBoff, Seunggeun Lee, Xihao Li, Zilin Li, Elise Lim, D. Y. Lin, Xihong Lin, Simin Liu, Yingchang Lu, JoAnn E. Manson, Lisa W. Martin, Caitlin McHugh, Julie Mikulla, Solomon K. Musani, Maggie Ng, Deborah A. Nickerson, Nicholette Palmer, James A. Perry, Ulrike Peters, Michael Preuß, Qibin Qi, Laura M. Raffield, Laura J. Rasmussen‐Torvik, Alex P. Reiner, Emily M. Russell, Colleen M. Sitlani, Jennifer A. Smith, Cassandra N. Spracklen, Tao Wang, Zhe Wang, Jennifer Wessel, Hanfei Xu, Mohammad Yaser, Sachiko Yoneyama, Kendra A. Young, Jingwen Zhang, Xinruo Zhang, Hufeng Zhou, Xiaofeng Zhu, Sebastian Zoellner, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Larry Bielak, Joshua C. Bis
Genetic Ancestry in Lung-Function Predictions
Rajesh Kumar, Max A. Seibold, Melinda C. Aldrich, L. Keoki Williams, Alex P. Reiner, Laura A. Colangelo, Joshua Galanter, Christopher R. Gignoux, Donglei Hu, Śaunak Sen, Shweta Choudhry, Edward L. Peterson, José Rodríguez‐Santana, William Rodríguez-Cintrón, Michael A. Nalls, Tennille S. Leak, Ellen S. O’Meara, Bernd Meibohm, Stephen B. Kritchevsky, Rongling Li, Tamara B. Harris, Deborah A. Nickerson, Myriam Fornage, Paul Enright, Elad Ziv, Lewis J. Smith, Kiang Liu, Esteban G. Burchard
Mutations in <i>RSPH1</i> Cause Primary Ciliary Dyskinesia with a Unique Clinical and Ciliary Phenotype
Michael R. Knowles, Lawrence E. Ostrowski, Margaret W. Leigh, Patrick R. Sears, Stephanie D. Davis, Whitney Wolf, Milan J. Hazucha, Johnny L. Carson, Kenneth N. Olivier, Scott D. Sagel, Margaret Rosenfeld, Thomas W. Ferkol, Sharon Dell, Carlos Milla, Scott H. Randell, Weining Yin, Aruna Sannuti, Hilda Metjian, Peadar G. Noone, Peter J. Noone, Christina A. Olson, Michael V. Patrone, Hong Dang, Hye Seung Lee, Toby W. Hurd, Heon Yung Gee, Edgar A. Otto, Jan Halbritter, Stefan Kohl, Martin Kircher, Jeffrey P. Krischer, Michael J. Bamshad, Deborah A. Nickerson, Friedhelm Hildebrandt, Jay Shendure, Maimoona A. Zariwala
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