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Stefan Mundlos

ResearcherPublications, citations & collaboration network

Stefan Mundlos is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Stefan Mundlos have?

ScholarIQindexed works

Stefan Mundlos has 673 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Stefan Mundlos have?

ScholarIQcitation count

Stefan Mundlos has 49,654 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Stefan Mundlos?

ScholarIQh-index

Stefan Mundlos has an h-index of 110 in OpenAlex.

What is the i10-index of Stefan Mundlos?

ScholarIQi10-index

Stefan Mundlos has an i10-index of 351 in OpenAlex.

What is the ORCID of Stefan Mundlos?

ScholarIQorcid

The ORCID for Stefan Mundlos is on the source record.

What is the OpenAlex record for Stefan Mundlos?

ScholarIQopenalex

The OpenAlex for Stefan Mundlos is on the source record.

What are the most-cited papers on Stefan Mundlos?

ScholarIQmost cited works
Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development
Florian Otto, Anders Thornell, Tessa Crompton, Angela Denzel, Kimberly Gilmour, Ian Rosewell, Gordon Stamp, Rosa Beddington, Stefan Mundlos, Bjørn R. Olsen, Paul B. Selby, Michael J. Owen
Cell. 19972,820 CitationsOPEN ACCESS
Nosology and classification of genetic skeletal disorders: 2019 revision
Geert Mortier, Daniel H. Cohn, Valérie Cormier‐Daire, Christine M Hall, Deborah Krakow, Stefan Mundlos, Gen Nishimura, Stephen P. Robertson, Luca Sangiorgi, Ravi Savarirayan, David Sillence, Andrea Superti‐Furga, Sheila Unger, Matthew L. Warman
American Journal of Medical Genetics Part A. 2019617 Citations
Nosology and classification of genetic skeletal disorders: 2015 revision
Luisa Bonafé, Valérie Cormier‐Daire, Christine M Hall, Ralph Lachman, Geert Mortier, Stefan Mundlos, Gen Nishimura, Luca Sangiorgi, Ravi Savarirayan, David Sillence, Jürgen W. Spranger, Andrea Superti‐Furga, Matthew L. Warman, Sheila Unger
American Journal of Medical Genetics Part A. 2015567 Citations
GestaltMatcher facilitates rare disease matching using facial phenotype descriptors
Tzung‐Chien Hsieh, Aviram Bar-Haim, Shahida Moosa, Nadja Ehmke, Karen W. Gripp, Jean Tori Pantel, Magdalena Danyel, Martin A. Mensah, Denise Horn, Stanislav Rosnev, Nicole Fleischer, Guilherme Bonini, Alexander Hustinx, Alexander Schmid, Alexej Knaus, Behnam Javanmardi, Hannah Klinkhammer, Hellen Lesmann, Sugirthan Sivalingam, Tom Kamphans, Wolfgang Meiswinkel, Frédéric Ebstein, Elke Krüger, Sébastien Küry, Stéphane Bezieau, Axel Schmidt, Sophia Peters, Hartmut Engels, Elisabeth Mangold, Martina Kreiß, Kirsten Cremer, Claudia Perne, Regina C. Betz, Tim Bender, Kathrin Grundmann‐Hauser, Tobias B. Haack, Matias Wagner, Theresa Brunet, Heidi Beate Bentzen, Luisa Averdunk, Kimberly Christine Coetzer, Gholson J. Lyon, Malte Spielmann, Christian P. Schaaf, Stefan Mundlos, Markus M. Nöthen, Peter Krawitz
Nature Genetics. 2022220 CitationsOPEN ACCESS

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