ScholarIQanswers from OpenAlex & ORCID
Mennat Mehrez
ResearcherPublications, citations & collaboration network
Mennat Mehrez is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Mennat Mehrez have?
ScholarIQindexed works
Mennat Mehrez has 27 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Mennat Mehrez have?
ScholarIQcitation count
Mennat Mehrez has 264 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Mennat Mehrez?
ScholarIQh-index
Mennat Mehrez has an h-index of 9 in OpenAlex.
What is the i10-index of Mennat Mehrez?
ScholarIQi10-index
Mennat Mehrez has an i10-index of 9 in OpenAlex.
What is the ORCID of Mennat Mehrez?
ScholarIQorcid
The ORCID for Mennat Mehrez is on the source record.
What is the OpenAlex record for Mennat Mehrez?
ScholarIQopenalex
The OpenAlex for Mennat Mehrez is on the source record.
What are the most-cited papers on Mennat Mehrez?
ScholarIQmost cited works
Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the cilium
José A. Caparrós‐Martín, Alessandro De Luca, François Cartault, Mona Aglan, Samia A. Temtamy, Ghada A. Otaify, Mennat Mehrez, María Valencia, Laura Vázquez, Jean‐Luc Alessandri, Julián Nevado, Inmaculada Rueda‐Arenas, Karen E. Heath, M. Cristina Digilio, Bruno Dallapiccola, Judith A. Goodship, Pleasantine Mill, Pablo Lapunzina, Víctor L. Ruiz‐Pérez
Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome
Adrián Palencia‐Campos, Phillip C. Aoto, Erik M.F. Machal, Ana Rivera‐Barahona, Patricia Soto‐Bielicka, Daniela Bertinetti, Blaine Baker, Lily Vu, Francesca Piceci‐Sparascio, Isabella Torrente, Eveline Boudin, Silke Peeters, Wim Van Hul, Céline Huber, Dominique Bonneau, Michael S. Hildebrand, Matthew Coleman, Melanie Bahlo, Mark F. Bennett, Amy Schneider, Ingrid E. Scheffer, Maria Kibæk, Britta Schlott Kristiansen, Mahmoud Y. Issa, Mennat Mehrez, Samira Ismail, Jair Tenorio, Gaoyang Li, Bjørn Steen Skålhegg, Ghada A. Otaify, Samia A. Temtamy, Mona Aglan, Aia Elise Jønch, Alessandro De Luca, Geert Mortier, Valérie Cormier‐Daire, Alban Ziegler, Mathew Wallis, Pablo Lapunzina, Friedrich W. Herberg, Susan S. Taylor, Víctor L. Ruiz‐Pérez
Gene Mutations of the Three Ectodysplasin Pathway Key Players (EDA, EDAR, and EDARADD) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations
Hoda A. Ahmed, Ghada El‐Kamah, Eman Rabie, Mostafa I. Mostafa, Maha R. Abouzaid, Nehal F. Hassib, Mennat Mehrez, Mohamed Abdel Kader, Yasmine H. Mohsen, Suher Zada, Khalda Amr, Inas S. M. Sayed
Expanding the mutation and clinical spectrum of Roberts syndrome
Hanan H. Afifi, Ghada M. H. Abdel‐Salam, Maha M. Eid, Angie M.S. Tosson, Wafaa Gh. Shousha, Amira A. Abdel Azeem, Mona K. Farag, Mennat Mehrez, Khaled R. Gaber
Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect
Ghada A. Otaify, Mohamed S. Abdel‐Hamid, Mennat Mehrez, Eman H. A. Aboul-Ezz, Maha S. Zaki, Mona Aglan, Samia A. Temtamy