ScholarIQanswers from OpenAlex & ORCID
Gert‐Jan B. van Ommen
ResearcherPublications, citations & collaboration network
Gert‐Jan B. van Ommen is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Gert‐Jan B. van Ommen have?
ScholarIQindexed works
Gert‐Jan B. van Ommen has 254 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Gert‐Jan B. van Ommen have?
ScholarIQcitation count
Gert‐Jan B. van Ommen has 30,083 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Gert‐Jan B. van Ommen?
ScholarIQh-index
Gert‐Jan B. van Ommen has an h-index of 72 in OpenAlex.
What is the i10-index of Gert‐Jan B. van Ommen?
ScholarIQi10-index
Gert‐Jan B. van Ommen has an i10-index of 174 in OpenAlex.
What is the ORCID of Gert‐Jan B. van Ommen?
ScholarIQorcid
The ORCID for Gert‐Jan B. van Ommen is on the source record.
What is the OpenAlex record for Gert‐Jan B. van Ommen?
ScholarIQopenalex
The OpenAlex for Gert‐Jan B. van Ommen is on the source record.
What are the most-cited papers on Gert‐Jan B. van Ommen?
ScholarIQmost cited works
Transcriptome and genome sequencing uncovers functional variation in humans
Tuuli Lappalainen, Michael Sammeth, Marc R. Friedländer, Peter A.C. ’t Hoen, Jean Monlong, Manuel A. Rivas, Mar Gonzàlez-Porta, Natalja Kurbatova, Thasso Griebel, Pedro G. Ferreira, Matthias Barann, Thomas Wieland, Liliana Greger, Maarten van Iterson, Jonas Carlsson Almlöf, Paolo Ribeca, Irina Pulyakhina, Daniela Esser, Thomas Giger, Andrew Tikhonov, Marc Sultan, Gabrielle Bertier, Daniel G. MacArthur, Monkol Lek, Esther Lizano, Henk P.J. Buermans, Ismaël Padioleau, Thomas Schwarzmayr, Olof Karlberg, Halit Ongen, Helena Kilpinen, Sergi Beltrán, Marta Gut, Katja Kahlem, Vyacheslav Amstislavskiy, Oliver Stegle, Matti Pirinen, Stephen B. Montgomery, Peter Donnelly, Mark I. McCarthy, Paul Flicek, Tim M. Strom, Hans Lehrach, Stefan Schreiber, Ralf Sudbrak, Ãngel Carracedo, Stylianos E. Antonarakis, Robert Häsler, Ann‐Christine Syvänen, Gert‐Jan B. van Ommen, Alvis Brāzma, Thomas Meitinger, Philip Rosenstiel, Roderic Guigó, Marta Gut, Xavier Estivill, Emmanouil T. Dermitzakis
Whole-genome sequence variation, population structure and demographic history of the Dutch population
Laurent C. Francioli, Androniki Menelaou, Sara L. Pulit, Clara C. Elbers, Wigard P. Kloosterman, Jessica van Setten, Isaäc J. Nijman, Ivo Renkens, Paul I. W. de Bakker, Freerk van Dijk, Pieter B. Neerincx, Patrick Deelen, Alexandros Kanterakis, Martijn Dijkstra, Heorhiy Byelas, K. Joeri van der Velde, Mathieu Platteel, Morris A. Swertz, Cisca Wijmenga, Pier Francesco Palamara, Itsik Pe’er, Kai Ye, Eric-Wubbo Lameijer, Matthijs H. Moed, Marian Beekman, Anton J. M. de Craen, H Eka D Suchiman, P. Eline Slagboom, Victor Guryev, Abdel Abdellaoui, Jouke‐Jan Hottenga, Mathijs Kattenberg, Gonneke Willemsen, Dorret I. Boomsma, Jin‐Moo Lee, Lennart C. Karssen, Najaf Amin, Fernando Rivadeneira, Aaron Isaacs, Albert Hofman, André G. Uitterlinden, Cornelia M. van Duijn, Mannis van Oven, Manfred Kayser, Martijn Vermaat, Jeroen F. J. Laros, Johan T. den Dunnen, David van Enckevort, Hailiang Mei, Mingkun Li, Mark Stoneking, Barbera D. C. van Schaik, Jan Bot, Tobias Marschall, Alexander Schönhuth, Jayne Y. Hehir‐Kwa, Robert E. Handsaker, Paz Polak, Mashaal Sohail, Dana Vuzman, Karol Estrada, Steven A. McCarroll, Shamil Sunyaev, Fereydoun Hormozdiari, Vyacheslav Koval, Carolina Medina‐Gómez, Ben Oostra, Jan H. Veldink, Leonard H. van den Berg, Steven J. Pitts, Shobha Potluri, Purnima Sundar, David R. Cox, Peter de Knijff, Qibin Li, Yingrui Li, Yuanping Du, Ruoyan Chen, Hongzhi Cao, Jun Wang, Ning Li, Sujie Cao, Jasper Bovenberg, Gert‐Jan B. van Ommen
Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles
Carl E.G. Bruder, Arkadiusz Piotrowski, Antoinet A.C.J. Gijsbers, Robin Andersson, Stephen W. Erickson, Teresita Díaz de Ståhl, Uwe Menzel, Johanna Sandgren, Désirée von Tell, Andrzej Poplawski, Michael Crowley, Chiquito Crasto, E. Christopher Partridge, Hemant K. Tiwari, David B. Allison, Jan Komorowski, Gert‐Jan B. van Ommen, Dorret I. Boomsma, Nancy L. Pedersen, Johan T. den Dunnen, Karin Wirdefeldt, Jan P. Dumanski
Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease
Jeroen Roelfsema, Stefan J. White, Yavuz Ariyürek, Deborah Bartholdi, Dunja Niedrist, Francesco Papadia, Carlos A. Bacino, Johan T. den Dunnen, Gert‐Jan B. van Ommen, Martijn H. Breuning, Raoul C. M. Hennekam, Dorien J.M. Peters