ScholarIQanswers from OpenAlex & ORCID
Arnold Münnich
ResearcherPublications, citations & collaboration network
Arnold Münnich is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Arnold Münnich have?
ScholarIQindexed works
Arnold Münnich has 952 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Arnold Münnich have?
ScholarIQcitation count
Arnold Münnich has 68,170 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Arnold Münnich?
ScholarIQh-index
Arnold Münnich has an h-index of 130 in OpenAlex.
What is the i10-index of Arnold Münnich?
ScholarIQi10-index
Arnold Münnich has an i10-index of 640 in OpenAlex.
What is the ORCID of Arnold Münnich?
ScholarIQorcid
The ORCID for Arnold Münnich is on the source record.
What is the OpenAlex record for Arnold Münnich?
ScholarIQopenalex
The OpenAlex for Arnold Münnich is on the source record.
What are the most-cited papers on Arnold Münnich?
ScholarIQmost cited works
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling
Rainer Döffinger, Asma Smahi, Christine Bessia, Frédéric Geissmann, Jacqueline Feinberg, Anne Durandy, Christine Bodemer, Sue Kenwrick, Sophie Dupuis‐Girod, Stéphane Blanche, Philip Wood, Smail Hadj Rabia, Denis J. Headon, Paul A. Overbeek, Françoise Le Deist, Steven M. Holland, Kiran Belani, Dinakantha Kumararatne, Alain Fischer, Ralph Shapiro, Mary Ellen Conley, Eric Reimund, Hermann Kalhoff, Mario Abinun, Arnold Münnich, Alain Israël, Gilles Courtois, Jean‐Laurent Casanova
De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy
Giulia Barcia, Matthew R. Fleming, Aline Deligniere, Valeswara‐Rao Gazula, Maile R. Brown, Maéva Langouët, Haijun Chen, Jack Kronengold, Avinash Abhyankar, Roberta Cilio, Patrick Nitschké, Anna Kamińska, Nathalie Boddaert, Jean‐Laurent Casanova, Isabelle Desguerre, Arnold Münnich, Olivier Dulac, Leonard K. Kaczmarek, Laurence Colleaux, Rima Nabbout
SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)
Valérie Belin, Véronica Cusin, Géraldine Viot, Delphine Girlich, Annick Toutain, Anne Moncla, Michel Vekemans, Martine Le Merrer, Arnold Münnich, Valérie Cormier‐Daire
Phenotype and genotype in 101 males with X-linked creatine transporter deficiency
Jiddeke M. van de Kamp, Ofir T. Betsalel, Saadet Mercimek‐Mahmutoglu, Lara Abulhoul, Stephanie Grünewald, Irina Anselm, Hatem Azzouz, Drago Bratkovic, Arjan de Brouwer, Ben C.J. Hamel, Tjitske Kleefstra, Helger G. Yntema, Jaume Campistol, Marta Vilaseca, David Cheillan, Marc D’Hooghe, Luísa Diogo, Paula Garcia, Carla Valongo, Maria José Fonseca, Suzanna G.M. Frints, Bridget Wilcken, Sigrun von der Haar, Hanne Meijers‐Heijboer, Floris C. Hofstede, Diana Johnson, Sarina G. Kant, Laurence Lion‐François, G. Pitelet, Nicola Longo, J A Maat-Kievit, João Monteiro, Arnold Münnich, Ania C. Muntau, Marie‐Cécile Nassogne, Hitoshi Osaka, Katrin Õunap, Jean-Marc Pinard, Susana Quijano‐Roy, Imke Poggenburg, Nicola Poplawski, Omar Abdul‐Rahman, Antònia Ribes, Ángela Arias, Joy Yaplito‐Lee, Andreas Schulze, Charles E. Schwartz, Susanne Schwenger, G. Soares, Yves Sznajer, Vassili Valayannopoulos, Hilde Van Esch, Stephan Waltz, Mirjam M. C. Wamelink, Petra J. W. Pouwels, Abdellatif Errami, Marjo S. van der Knaap, C. Jakobs, Grazia M.S. Mancini, Gajja S. Salomons
Mutational, functional, and expression studies of the<i>TCF4</i>gene in Pitt-Hopkins syndrome
Loïc de Pontual, Yves Mathieu, Christelle Golzio, Marlène Rio, Valérie Malan, Nathalie Boddaert, Christine Soufflet, Capucine Pïcard, Anne Durandy, Angus Dobbie, Delphine Héron, Bertrand Isidor, Jacques Motté, Ruth Newburry-Ecob, Laurent Pasquier, Marc Tardieu, G��raldine Viot, Francis Jaubert, Arnold Münnich, Laurence Colleaux, Michel Vekemans, Heather Etchevers, Stanislas Lyonnet, Jeanne Amiel