Upload Records Snowball Search Search OpenAlex
About the database ScholarIQanswers from OpenAlex & ORCID
How has Mennat Mehrez's publication output changed over time?
ScholarIQpublication output · 2013–2023
Output grew0% over the shown period — from 1 works in 2013 to 1 in 2023.
1
3
2
1
1
1
1
1
20132015201720182019202020212023
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
S166515463. 201555 CitationsOPEN ACCESS
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
S134425043. 202054 CitationsOPEN ACCESS
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
Genes. 202122 CitationsOPEN ACCESS
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
S82432819. 201519 CitationsOPEN ACCESS
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
S170889201. 201818 Citations
Related on ScholarIQ
National Human Genome Research Institute
Institution
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
Paper
Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome
Paper
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
Paper
Expanding the mutation and clinical spectrum of Roberts syndrome
Paper
Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect
Paper