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Ben A. Oostra

ResearcherPublications, citations & collaboration network

Ben A. Oostra is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Ben A. Oostra have?

ScholarIQindexed works

Ben A. Oostra has 259 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Ben A. Oostra have?

ScholarIQcitation count

Ben A. Oostra has 36,023 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Ben A. Oostra?

ScholarIQh-index

Ben A. Oostra has an h-index of 91 in OpenAlex.

What is the i10-index of Ben A. Oostra?

ScholarIQi10-index

Ben A. Oostra has an i10-index of 194 in OpenAlex.

What is the OpenAlex record for Ben A. Oostra?

ScholarIQopenalex

The OpenAlex for Ben A. Oostra is on the source record.

What are the most-cited papers on Ben A. Oostra?

ScholarIQmost cited works
Mutations in the <i>DJ-1</i> Gene Associated with Autosomal Recessive Early-Onset Parkinsonism
Vincenzo Bonifati, Patrizia Rizzu, Marijke J. van Baren, Onno Schaap, Guido J. Breedveld, Elmar Krieger, Marieke Dekker, Ferdinando Squitieri, Pablo Ibáñez, Marijke Joosse, Jeroen W. van Dongen, Nicola Vanacore, John C. van Swieten, Alexis Brice, G. Meco, Cornelia M. van Duijn, Ben A. Oostra, Peter Heutink
Science. 20032,791 Citations
Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1
Kimberly A. McAllister, K.M. Grogg, David W. Johnson, Carol J. Gallione, Melanie A. Baldwin, Charles E. Jackson, E.A. Helmbold, Dorene S. Markel, Wendy McKinnon, J. Murrel, Mary Kay McCormick, M. A. Pericak‐Vance, Peter Heutink, Ben A. Oostra, T. Haitjema, C.J.J. Westerman, Mary Porteous, Alan E. Guttmacher, Michelle Letarte, Douglas A. Marchuk
Nature Genetics. 19941,503 CitationsOPEN ACCESS
Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis
Ingrid M.B.H. van de Laar, Rogier A. Oldenburg, Gerard Pals, Jolien W. Roos‐Hesselink, Bianca M. de Graaf, Judith M.A. Verhagen, Yvonne M. Hoedemaekers, Rob Willemsen, Lies‐Anne Severijnen, Hanka Venselaar, Gert Vriend, Peter M. T. Pattynama, Margriet Collée, Daniëlle Majoor‐Krakauer, Don Poldermans, Ingrid M.E. Frohn-Mulder, Dimitra Micha, Janneke Timmermans, Yvonne Hilhorst‐Hofstee, Sita Bierma‐Zeinstra, Patrick J. Willems, Johan M. Kros, E.H. Oei, Ben A. Oostra, Marja W. Wessels, Aida M. Bertoli‐Avella
Nature Genetics. 2011677 Citations
Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949)
Gail Davies, Nicola J. Armstrong, Joshua C. Bis, Jan Bressler, Vincent Chouraki, Sudheer Giddaluru, Edith Hofer, Carla A. Ibrahim‐Verbaas, Mirna Kirin, Jari Lahti, S J van der Lee, Stéphanie Le Hellard, Tsan Liu, Riccardo E. Marioni, Christopher Oldmeadow, Iris Postmus, Albert V. Smith, Jennifer A. Smith, Anbupalam Thalamuthu, Russell Thomson, Véronique Vitart, Jiao Wang, Lei Yu, Lina Zgaga, Wei Zhao, Ruth Boxall, Sarah E. Harris, W. David Hill, David C. Liewald, Michelle Luciano, Hieab H.H. Adams, David Ames, Najaf Amin, Philippe Amouyel, Amelia A. Assareh, Rhoda Au, James T. Becker, Alexa Beiser, Claudine Berr, Lars Bertram, Eric Boerwinkle, B. M. Buckley, Harry Campbell, Janie Corley, Philip L. De Jager, Carole Dufouil, Johan G. Eriksson, Thomas Espeseth, Jessica D. Faul, Ian Ford, Generation Scotland, Rebecca F. Gottesman, M E Griswold, Vilmundur Guðnason, Tamara B. Harris, G. Heiss, A Hofman, E.G. Holliday, Jennifer E. Huffman, Sharon L. R. Kardia, Nicole A. Kochan, D S Knopman, John B. Kwok, J-C Lambert, Teresa Lee, G. Li, Shu Li, M Loitfelder, O L Lopez, Astri J. Lundervold, Annamari Lundqvist, Karen A. Mather, S S Mirza, Lars Nyberg, Ben A. Oostra, Aarno Palotie, Goran Papenberg, Alison Pattie, Katja Petrovic, Ozren Polašek, Bruce M. Psaty, Paul Redmond, Simone Reppermund, Jerome I. Rotter, Helena Schmidt, Maaike Schuur, P W Schofield, Rodney J. Scott, V M Steen, David J. Stott, John C. van Swieten, Kent D. Taylor, Julian N. Trollor, Stella Trompet, André G. Uitterlinden, Galit Weinstein, Elisabeth Widén, B. Gwen Windham, J. Wouter Jukema, A F Wright
Molecular Psychiatry. 2015413 CitationsOPEN ACCESS
<i>ATP13A2</i> missense mutations in juvenile parkinsonism and young onset Parkinson disease
Alessio Di Fonzo, Hsin Fen Chien, Mariana P. Socal, Sabrina Giraudo, C. Tassorelli, Gianni Iliceto, Giovanni Fabbrini, R. Marconi, E. Fincati, Giovanni Abbruzzese, P. Marini, Ferdinando Squitieri, M.W.I.M. Horstink, P. Montagna, A. Dalla Libera, Fabrizio Stocchi, Stefano Goldwurm, Joaquim J. Ferreira, G. Meco, E. Martignoni, Leonardo Lopiano, Laura Bannach Jardim, Ben A. Oostra, Egberto Reis Barbosa, The Italian Parkinson Genetics Network, V. Bonifati
Neurology. 2007339 Citations

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