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Raoul C. M. Hennekam

ResearcherPublications, citations & collaboration network

Raoul C. M. Hennekam is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Raoul C. M. Hennekam have?

ScholarIQindexed works

Raoul C. M. Hennekam has 841 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Raoul C. M. Hennekam have?

ScholarIQcitation count

Raoul C. M. Hennekam has 46,576 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Raoul C. M. Hennekam?

ScholarIQh-index

Raoul C. M. Hennekam has an h-index of 108 in OpenAlex.

What is the i10-index of Raoul C. M. Hennekam?

ScholarIQi10-index

Raoul C. M. Hennekam has an i10-index of 432 in OpenAlex.

What is the ORCID of Raoul C. M. Hennekam?

ScholarIQorcid

The ORCID for Raoul C. M. Hennekam is on the source record.

What is the OpenAlex record for Raoul C. M. Hennekam?

ScholarIQopenalex

The OpenAlex for Raoul C. M. Hennekam is on the source record.

What are the most-cited papers on Raoul C. M. Hennekam?

ScholarIQmost cited works
Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP
Fred Petrif, Rachel H. Giles, Hans G. Dauwerse, Jasper J. Saris, Raoul C. M. Hennekam, Mitsuo Masuno, Niels Tommerup, Gert‐Jan B. van Ommen, Richard H. Goodman, Dorien J.M. Peters, Martijn H. Breuning
Nature. 19951,224 Citations
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
The American Journal of Human Genetics. 2005484 CitationsOPEN ACCESS
Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome
Gillian Rice, Teresa Patrick, Rekha Parmar, Claire Taylor, Alec Aeby, Jean Aicardi, Rafael Artuch, Simon Attard Montalto, Carlos A. Bacino, Bruno Barroso, Peter Baxter, Willam S. Benko, Carsten Bergmann, Enrico Bertini, Roberta Biancheri, Edward Blair, Nenad Blau, David T. Bonthron, Tracy A. Briggs, Louise Brueton, Han G. Brunner, Christopher J. Burke, Ian Carr, Daniel R. Carvalho, Kate Chandler, H.‐J. Christen, Peter Corry, Frances M. Cowan, Helen Cox, Stefano D’Arrigo, John Dean, Corinne De Laet, Claudine De Praeter, Catherine Déry, Colin D. Ferrie, Kim Flintoff, Suzanna G.M. Frints, Àngels García‐Cazorla, Blanca Gener, Cyril Goizet, Françoise Goutières, Andrew Green, Agnès Guët, Ben C.J. Hamel, Bruce E. Hayward, Arvid Heiberg, Raoul C. M. Hennekam, Marie Husson, Andrew P. Jackson, Rasieka Jayatunga, Yong‐hui Jiang, Sarina G. Kant, Amy Kao, Mary D. King, Helen Kingston, Joerg Klepper, Marjo S. van der Knaap, Andrew J. Kornberg, Dieter Kotzot, W Kratzer, Didier Lacombe, Lieven Lagae, P. Landrieu, Giovanni Lanzi, Andrea Leitch, Ming Lim, John H. Livingston, Charles Marques Lourenço, E G Hermione Lyall, Sally Ann Lynch, Michael J. Lyons, Daphna Marom, John P. McClure, Robert McWilliam, Serge B. Melançon, Leena Mewasingh, Marie‐Laure Moutard, Ken K. Nischal, John R. Østergaard, Julie Prendiville, Magnhild Rasmussen, R. Curtis Rogers, Dominique Roland, Elisabeth Rosser, Kevin Rostásy, Agathe Roubertie, Amparo Sanchís, Raphael Schiffmann, Sabine Scholl‐Bürgi, Sunita Seal, Stavit A. Shalev, Concepción Sierra Córcoles, Gyan P. Sinha, Doriette Soler, Ronen Spiegel, John B.P. Stephenson, Uta Tacke, Tiong Yang Tan, Marianne Till, John Tolmie
The American Journal of Human Genetics. 2007453 CitationsOPEN ACCESS
HNF1B Mutations Associate with Hypomagnesemia and Renal Magnesium Wasting
Shazia Adalat, Adrian S. Woolf, Karen A. Johnstone, Andrea Wirsing, Lorna W. Harries, David A. Long, Raoul C. M. Hennekam, Sarah Ledermann, Lesley Rees, William van’t Hoff, Stephen D. Marks, Richard S. Trompeter, Kjell Tullus, Paul J.D. Winyard, Janette Cansick, Imran Mushtaq, H.K. Dhillon, Coralie Bingham, Emma L. Edghill, Rukshana Shroff, Horia Stanescu, Gerhart U. Ryffel, Sian Ellard, Detlef Böckenhauer
Journal of the American Society of Nephrology. 2009278 CitationsOPEN ACCESS
Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III
H.‐J. Lüdecke, Jörg Schaper, Peter Meinecke, Parastoo Momeni, Simon Groß, D. von Holtum, H. Hirche, Marc Abramowicz, Beate Albrecht, Can Apacik, H.‐J. Christen, U. Claussen, Koenraad Devriendt, Elisabeth Fastnacht, A. Forderer, U Friedrich, Thj Goodship, M. Greiwe, Henning Hamm, Raoul C. M. Hennekam, Georg Klaus Hinkel, Maria Hoeltzenbein, Hülya Kayserili, F. Majewski, M Mathieu, Ross McLeod, Alina T. Midro, Ute Moog, Toshiro Nagai, Norio Niikawa, Karen Helene Ørstavik, E Plöchl, C. S. Seitz, Jörg Schmidtke, Lisbeth Tranebjærg, Masato Tsukahara, B Wittwer, Bernhard Zabel, Gabriele Gillessen‐Kaesbach, Bernhard Horsthemke
The American Journal of Human Genetics. 2001235 CitationsOPEN ACCESS

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