ScholarIQanswers from OpenAlex & ORCID
Joris A. Veltman
ResearcherPublications, citations & collaboration network
Joris A. Veltman is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Joris A. Veltman have?
ScholarIQindexed works
Joris A. Veltman has 403 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Joris A. Veltman have?
ScholarIQcitation count
Joris A. Veltman has 37,857 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Joris A. Veltman?
ScholarIQh-index
Joris A. Veltman has an h-index of 103 in OpenAlex.
What is the i10-index of Joris A. Veltman?
ScholarIQi10-index
Joris A. Veltman has an i10-index of 267 in OpenAlex.
What is the ORCID of Joris A. Veltman?
ScholarIQorcid
The ORCID for Joris A. Veltman is on the source record.
What is the OpenAlex record for Joris A. Veltman?
ScholarIQopenalex
The OpenAlex for Joris A. Veltman is on the source record.
What are the most-cited papers on Joris A. Veltman?
ScholarIQmost cited works
Disruption of the neurexin 1 gene is associated with schizophrenia
Dan Rujescu, Andrés Ingason, Sven Cichon, Olli Pietiläinen, Michael R. Barnes, Timothea Toulopoulou, Marco Picchioni, Evangelos Vassos, Ulrich Ettinger, Elvira Bramon, Robin Murray, Mirella Ruggeri, Sarah Tosato, Chiara Bonetto, Stacy Steinberg, Engilbert Sigurðsson, Thordur Sigmundsson, Hannes Pétursson, Arnaldur Gylfason, Pall I. Olason, Gudmundur Hardarsson, Guðrún A. Jónsdóttir, Ómar Gústafsson, Ragnheiður Fossdal, Ina Giegling, Hans‐Jürgen Möller, Annette M. Hartmann, Per Hoffmann, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Srdjan Djurovic, Ingrid Melle, Ole A. Andreassen, Thomas Folkmann Hansen, Thomas Werge, Lambertus A. Kiemeney, Barbara Franke, Joris A. Veltman, Jacobine E. Buizer‐Voskamp, GROUP Investigators, Chiara Sabatti, Roel A. Ophoff, Marcella Rietschel, Markus M. Nöthen, Kāri Stefánsson, Leena Peltonen, David St Clair, Hreinn Stefánsson, David Collier
Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta
Jutta Becker, Oliver Semler, Christian Gilissen, Yun Li, Hanno J. Bolz, Cecilia Giunta, Carsten Bergmann, Marianne Rohrbach, Friederike Koerber, Katharina Zimmermann, Petra de Vries, Brunhilde Wirth, Eckhard Schöenau, Bernd Wollnik, Joris A. Veltman, Alexander Hoischen, Christian Netzer