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Kenneth N. Olivier

ResearcherPublications, citations & collaboration network

Kenneth N. Olivier is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Kenneth N. Olivier have?

ScholarIQindexed works

Kenneth N. Olivier has 283 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Kenneth N. Olivier have?

ScholarIQcitation count

Kenneth N. Olivier has 31,964 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Kenneth N. Olivier?

ScholarIQh-index

Kenneth N. Olivier has an h-index of 75 in OpenAlex.

What is the i10-index of Kenneth N. Olivier?

ScholarIQi10-index

Kenneth N. Olivier has an i10-index of 163 in OpenAlex.

What is the OpenAlex record for Kenneth N. Olivier?

ScholarIQopenalex

The OpenAlex for Kenneth N. Olivier is on the source record.

What are the most-cited papers on Kenneth N. Olivier?

ScholarIQmost cited works
Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome
Amy P. Hsu, Elizabeth P. Sampaio, Javed Khan, Katherine R. Calvo, Jacob E. Lemieux, Smita Y. Patel, David M. Frucht, Donald C. Vinh, Roger Auth, Alexandra F. Freeman, Kenneth N. Olivier, Gülbû Uzel, Christa S. Zerbe, Christine Spalding, Stefania Pittaluga, Mark Raffeld, Douglas B. Kuhns, Li Ding, Michelle L. Paulson, Beatriz E. Marciano, Juan Gea‐Banacloche, Jordan S. Orange, Jennifer Cuellar‐Rodríguez, Dennis D. Hickstein, Steven M. Holland
Blood. 2011638 Citations
Adult-Onset Immunodeficiency in Thailand and Taiwan
Sarah Browne, Peter D. Burbelo, Ploenchan Chetchotisakd, Yupin Suputtamongkol, Sasisopin Kiertiburanakul, Pamela A. Shaw, Jennifer L. Kirk, Kamonwan Jutivorakool, Rifat Zaman, Li Ding, Amy P. Hsu, Smita Y. Patel, Kenneth N. Olivier, Viraphong Lulitanond, Piroon Mootsikapun, Siriluck Anunnatsiri, Nasikarn Angkasekwinai, Boonmee Sathapatayavongs, Po‐Ren Hsueh, Chi-Chang Shieh, Margaret R. Brown, Wanna Thongnoppakhun, Reginald J. Claypool, Elizabeth P. Sampaio, Charin Thepthai, Duangdao Waywa, Camilla Dacombe, Yona Reizes, Adrian M. Zelazny, Paul Saleeb, Lindsey B. Rosen, Allen Mo, Michael J. Iadarola, Steven M. Holland
New England Journal of Medicine. 2012556 CitationsOPEN ACCESS
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
American Journal of Respiratory and Critical Care Medicine. 2014230 Citations
Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia
Christina Austin‐Tse, Jan Halbritter, Maimoona A. Zariwala, Renée M. Gilberti, Heon Yung Gee, Nathan E. Hellman, Narendra Pathak, Yan Liu, Jennifer R. Panizzi, Ramila S. Patel‐King, Douglas Tritschler, Raqual Bower, Eileen O’Toole, Jonathan D. Porath, Toby W. Hurd, Moumita Chaki, Katrina A. Diaz, Stefan Kohl, Svjetlana Lovric, Daw‐Yang Hwang, Daniela A. Braun, Markus Schueler, Rannar Airik, Edgar A. Otto, Margaret W. Leigh, Peadar G. Noone, Johnny L. Carson, Stephanie D. Davis, Jessica E. Pittman, Thomas W. Ferkol, Jeffry J. Atkinson, Kenneth N. Olivier, Scott D. Sagel, Sharon Dell, Margaret Rosenfeld, Carlos Milla, Niki T. Loges, Heymut Omran, Mary E. Porter, Stephen M. King, Michael R. Knowles, Iain A. Drummond, Friedhelm Hildebrandt
The American Journal of Human Genetics. 2013206 CitationsOPEN ACCESS
ZMYND10 Is Mutated in Primary Ciliary Dyskinesia and Interacts with LRRC6
Maimoona A. Zariwala, Heon Yung Gee, Małgorzata Kurkowiak, Dalal A. Al-Mutairi, Margaret W. Leigh, Toby W. Hurd, Rim Hjeij, Sharon Dell, Moumita Chaki, Gerard W. Dougherty, Mohamed Adan, Philip C. Spear, Julián Esteve-Rudd, Niki T. Loges, Margaret Rosenfeld, Katrina A. Diaz, Heike Olbrich, Whitney Wolf, Eamonn Sheridan, Trevor F.C. Batten, Jan Halbritter, Jonathan D. Porath, Stefan Kohl, Svjetlana Lovric, Daw‐Yang Hwang, Jessica E. Pittman, Kimberlie A. Burns, Thomas W. Ferkol, Scott D. Sagel, Kenneth N. Olivier, Lucy Morgan, Claudius Werner, Johanna Raidt, Petra Pennekamp, Zhaoxia Sun, Weibin Zhou, Rannar Airik, S. Natarajan, Susan J. Allen, Israel Amirav, Dagmar Wieczorek, Kerstin Landwehr, Kim G. Nielsen, Nicolaus Schwerk, Jadranka Sertić, Gabriele Köhler, Joseph Washburn, Shawn Levy, Shuling Fan, Cordula Koerner‐Rettberg, Serge Amselem, David S. Williams, Brian J. Mitchell, Iain A. Drummond, Edgar A. Otto, Heymut Omran, Michael R. Knowles, Friedhelm Hildebrandt
The American Journal of Human Genetics. 2013206 CitationsOPEN ACCESS

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