ScholarIQanswers from OpenAlex & ORCID
David Fitzpatrick
ResearcherPublications, citations & collaboration network
David Fitzpatrick is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does David Fitzpatrick have?
ScholarIQindexed works
David Fitzpatrick has 564 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does David Fitzpatrick have?
ScholarIQcitation count
David Fitzpatrick has 40,055 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of David Fitzpatrick?
ScholarIQh-index
David Fitzpatrick has an h-index of 103 in OpenAlex.
What is the i10-index of David Fitzpatrick?
ScholarIQi10-index
David Fitzpatrick has an i10-index of 303 in OpenAlex.
What is the ORCID of David Fitzpatrick?
ScholarIQorcid
The ORCID for David Fitzpatrick is on the source record.
What is the OpenAlex record for David Fitzpatrick?
ScholarIQopenalex
The OpenAlex for David Fitzpatrick is on the source record.
What are the most-cited papers on David Fitzpatrick?
ScholarIQmost cited works
Mutations in SOX2 cause anophthalmia
Judy Fantes, Nicola Ragge, Sally Ann Lynch, Niolette I. McGill, J. R. O. Collin, Patricia N. Howard‐Peebles, Caroline Hayward, Anthony J. Vivian, Kathy Williamson, Veronica van Heyningen, David Fitzpatrick
PIONEER 1: Randomized Clinical Trial of the Efficacy and Safety of Oral Semaglutide Monotherapy in Comparison With Placebo in Patients With Type 2 Diabetes
Vanita R. Aroda, Julio Rosenstock, Yasuo Terauchi, Yüksel Altuntaş, Nebojsa M. Lalic, Enrique C. Morales Villegas, Ole Kleist Jeppesen, Erik Christiansen, CHRISTIN L. HERTZ, Martin Haluzı́k, PIONEER 1 Investigators, Krim Belkacem, Nabil Chiali, Samia Bourezane, R. Guermaz, P Popivanov, Ivaylo Lefterov, Tsvetalina Tankova, I Penchev, Martina Košková, Miroslava Hudcova, Alica Vesela, Anna Rancova, Martin Haluzı́k, Arihiro Kiyosue, Osamu Matsuoka, Satoshi Inoue, Yasuo Terauchi, Yasushi Fukushima, Yumiko Ide, R. Ortiz, Enrique Villegas, Albina Golovach, Diana Alpenidze, Elena Frolova, Elena Zhdanova, Ludmila Ruyatkina, О. Б. Ершова, Ю. Г. Самойлова, S. T. Zyangirova, Katarina Lalić, Nebojša Lalić, Teodora Beljić Živković, Hayriye Esra Ataoğlu, Okan Bakıner, A. D. Dayan, Mehmet Sargın, Meral Mert, Mine Adaş, Ömür Tabak, Yüksel Altuntaş, Alexander V. Murray, Ali Iranmanesh, Aron Schlau, Bram Wieskopf, Brian D. Snyder, Carl J. Griffin, Charles Fogarty, Charles Lovell, Dale Allison, David Fitzpatrick, David Grant, David C. Klonoff, Dwayne Williams, Eddie Armas, Eileen M. Palace, Gary Ruoff, Gilbert Martinez, Gilberto Perez, Harold Bays, Horia Tatu, James Maynard, Jeanne-Elyse Cedeno, Vanita R. Aroda, Jean Park, Jennefer Sutton, Joe Pouzar, John Bertsch, Jonathan Condit, Jorge Serje, Josel Cabaccan, Joseph Risser, Juan P. Frías, Julio Rosenstock, Kanagaratnam Sivalingam, Kelli Maw, Lenita Hanson, Liana K. Billings, Lisa Connery, Mario Juarez, Michael Lillestol, Neil Fraser, Paul Beckett, Ralph Wade, Raul Gaona, Richard F. W. Jackson, Robert DeLuca, Sady Alpizar, Sharon J. Herring, Stanley Stringam
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
Fadi F. Hamdan, Candace T. Myers, Patrick Cossette, Philippe Lemay, Dan Spiegelman, Alexandre D. Laporte, Christina Nassif, Ousmane Diallo, Jean Monlong, Maxime Cadieux‐Dion, Sylvia Dobrzeniecka, Caroline Meloche, Kyle Retterer, Megan T. Cho, Jill A. Rosenfeld, Weimin Bi, Christine Massicotte, Marguerite Miguet, Ledia Brunga, Brigid M. Regan, Kelly Mo, Cory Tam, Amy Schneider, Georgie Hollingsworth, David Fitzpatrick, Alan Donaldson, Natalie Canham, Edward Blair, Bronwyn Kerr, Andrew E. Fry, Rhys H. Thomas, Joss Shelagh, Jane A. Hurst, Helen Brittain, Moira Blyth, Robert Roger Lebel, Erica H. Gerkes, Laura Davis‐Keppen, Quinn Stein, Wendy K. Chung, Sara J. Dorison, Paul J. Benke, Emily Fassi, Nicole Corsten‐Janssen, Erik‐Jan Kamsteeg, Frédéric Tran Mau‐Them, Ange‐Line Bruel, Alain Verloès, Katrin Õunap, Monica H. Wojcik, Dara V.F. Albert, Sunita Venkateswaran, Tyson L. Ware, Dean Jones, Yu‐Chi Liu, Shekeeb S. Mohammad, Peyman Bizargity, Carlos A. Bacino, Vincenzo Leuzzi, Simone Martinelli, Bruno Dallapiccola, Marco Tartaglia, Lubov Blumkin, Klaas J. Wierenga, Gabriela Purcarin, James J. O’Byrne, Sylvia Stöckler, Anna Lehman, Boris Keren, Marie‐Christine Nouguès, Cyril Mignot, Stéphane Auvin, Caroline Nava, Susan M. Hiatt, Martina Bebin, Yunru Shao, Fernando Scaglia, Seema R. Lalani, Richard E. Frye, Imad T. Jarjour, Stéphanie Jacques, Renee-Myriam Boucher, Émilie Riou, Myriam Srour, Lionel Carmant, Anne Lortie, Philippe Major, Paola Diadori, François Dubeau, Guy D’Anjou, Guillaume Bourque, Samuel F. Berkovic, Lynette G. Sadleir, Philippe M. Campeau, Zoha Kibar, Ronald G. Lafrenière, Simon Girard, Saadet Mercimek‐Mahmutoglu, Cyrus Boelman, Guy A. Rouleau
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
Claire Redin, Harrison Brand, Ryan L. Collins, Tammy Kammin, Elyse Mitchell, Jennelle C. Hodge, Carrie Hanscom, Vamsee Pillalamarri, Catarina M. Seabra, Mary‐Alice Abbott, Omar Abdul‐Rahman, Erika Aberg, Rhett Adley, Sofía Lizeth Alcaráz‐Estrada, Fowzan S. Alkuraya, Yu An, MaryAnne Anderson, Caroline Antolik, Kwame Anyane‐Yeboa, Joan Atkin, Tina M. Bartell, Jonathan A. Bernstein, Elizabeth Beyer, Ian Blumenthal, Ernie M.H.F. Bongers, Eva H. Brilstra, Chester Brown, Hennie T. Brüggenwirth, Bert Callewaert, Colby Chiang, Ken Corning, Helen Cox, Edwin Cuppen, Benjamin Currall, Tom Cushing, D. David, Matthew A. Deardorff, Annelies Dheedene, Marc D’Hooghe, Bert B.A. de Vries, Dawn Earl, Heather Ferguson, Heather Fisher, David Fitzpatrick, Pamela Gerrol, Daniela Giachino, Joseph Glessner, Troy J. Gliem, Margo Grady, Brett H. Graham, Cristin Griffis, Karen W. Gripp, Andrea Gropman, Andrea Hanson‐Kahn, David J. Harris, Mark A. Hayden, R. Sean Hill, Ron Hochstenbach, Jodi D. Hoffman, Robert J. Hopkin, Monika Weisz Hubshman, A. Micheil Innes, Mira Irons, Melita Irving, Jessie C. Jacobsen, Sandra Janssens, Tamison Jewett, John P. Johnson, Marjolijn C.J. Jongmans, Stephen G. Kahler, David A. Koolen, Jerome Korzelius, Peter M. Kroisel, Yves Lacassie, William Lawless, Emmanuelle Lemyre, Kathleen A. Leppig, Alex V. Levin, Haibo Li, Hong Li, Eric C. Liao, Cynthia Lim, Edward J. Lose, Diane Lucente, Michael J. Macera, Poornima Manavalan, Giorgia Mandrile, Carlo Marcelis, Lauren Margolin, Tamara Mason, Diane Masser‐Frye, Michael McClellan, Cinthya J. Zepeda Mendoza, Björn Menten, Sjors Middelkamp, Liya Regina Mikami, Emily Moe, Shehla Mohammed, Tarja Mononen, Megan Mortenson
Heterozygous Mutations of OTX2 Cause Severe Ocular Malformations
Nicola Ragge, Alison G. M. Brown, Charlotte M. Poloschek, Birgit Lorenz, Richard A. Henderson, Michael W. Clarke, Isabelle Russell‐Eggitt, Alistair R. Fielder, Dianne Gerrelli, Juan Pedro Martı́nez-Barberá, Piers Ruddle, Jane A. Hurst, J. R. O. Collin, Alison Salt, Simon Timothy Cooper, Pamela J. Thompson, Sanjay M. Sisodiya, Kathleen A. Williamson, David Fitzpatrick, Veronica van Heyningen, Isabel M. Hanson