Samia A. Temtamy

6.7k citations

127 papers · 2.9k indexed · h-index 29

Genetics top 1%
Molecular Biology top 5%
Rheumatology top 2%
Surgery top 10%
Pediatrics, Perinatology and Child Health top 5%

Co-authors: Mona Aglan Jordan Miller Víctor L. Ruiz‐Pérez Pablo Lapunzina Eulalia Valencia José A. Caparrós‐Martín Víctor Martínez‐Glez Nagwa A. Meguid
Topics: Connective tissue disorders research (25 papers)Congenital limb and hand anomalies (17 papers)Genomic variations and chromosomal abnormalities (13 papers)
Cited by: Developmental Biology Genetics Rheumatology
Journals: Nature Genetics The American Journal of Human Genetics Human Molecular Genetics
Partner nations: Egypt United States Spain

In The Last Decade

Samia A. Temtamy

119 papers receiving 2.7k citations

Peers

Countries citing papers authored by Samia A. Temtamy

Since Specialization

Citations

This map shows the geographic impact of Samia A. Temtamy's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Samia A. Temtamy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Samia A. Temtamy more than expected).

Fields of papers citing papers by Samia A. Temtamy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Samia A. Temtamy. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Samia A. Temtamy. The network helps show where Samia A. Temtamy may publish in the future.

Co-authorship network of co-authors of Samia A. Temtamy

This figure shows the co-authorship network connecting the top 25 collaborators of Samia A. Temtamy. A scholar is included among the top collaborators of Samia A. Temtamy based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Samia A. Temtamy. Samia A. Temtamy is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	3D assessment of intervertebral disc degeneration in zebrafish identifies changes in bone density that prime disc disease 2021 ·Bone Research ·Érika Kague,Francesco Turci,(unknown),(unknown),Kate Robson Brown,Mona Aglan,Ghada A. Otaify,Samia A. Temtamy,Víctor L. Ruiz‐Pérez,Stephen Cross,C. Patrick Royall,P. Eckhard Witten,Chrissy L. Hammond	39
2	Biallelic truncating variants in MAPKAPK5 cause a new developmental disorder involving neurological, cardiac, and facial anomalies combined with synpolydactyly 2021 ·Genetics in Medicine ·Denise Horn,(unknown),(unknown),(unknown),Julián Nevado,(unknown),Nadja Ehmke,Pablo Lapunzina,Ghada A. Otaify,Samia A. Temtamy,Mona Aglan,Felix Boschann,Víctor L. Ruiz‐Pérez	5
3	Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate 2019 ·Disease Models & Mechanisms ·Roberta Besio,(unknown),Laura Leoni,Lina Cipolla,Simone Sabbioneda,Marco Biggiogera,Monica Mottes,Mona Aglan,Ghada A. Otaify,Samia A. Temtamy,Antonio Rossi,Antonella Forlino	52
4	Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification 2019 ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Mona Aglan,Samira Ismail,(unknown),Ghada A. Otaify,(unknown),(unknown),(unknown),Samia A. Temtamy	1
5	ROBERTS SYNDROME: CLINICAL AND CYTOGENETIC STUDIES IN 8 EGYPTIAN PATIENTS AND MOLECULAR STUDIES IN 4 PATIENTS WITH GENOTYPE/PHENOTYPE CORRELATION. 2018 ·PubMed ·Somaia Ismail,Mona L. Essawi,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Ghada A. Otaify,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Mona Aglan,Samia A. Temtamy	4
6	Genetics and Genomic Medicine in Egypt: steady pace 2017 ·Molecular Genetics & Genomic Medicine ·Samia A. Temtamy,(unknown)	7
7	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 2015 ·Human Molecular Genetics ·José A. Caparrós‐Martín,Alessandro De Luca,François Cartault,Mona Aglan,Samia A. Temtamy,Ghada A. Otaify,(unknown),Eulalia Valencia,(unknown),(unknown),Julián Nevado,(unknown),Karen E. Heath,M. Cristina Digilio,Bruno Dallapiccola,Judith A. Goodship,Pleasantine Mill,Pablo Lapunzina,Víctor L. Ruiz‐Pérez	42
8	Report of a newly indentified patient with mutations in BMP1 and underlying pathogenetic aspects 2014 ·American Journal of Medical Genetics Part A ·Eulalia Valencia,José A. Caparrós‐Martín,Ma Salomé Sirerol-Piquer,José Manuel García‐Verdugo,Víctor Martínez‐Glez,Pablo Lapunzina,Samia A. Temtamy,Mona Aglan,Allan M. Lund,Peter G. J. Nikkels,Víctor L. Ruiz‐Pérez,Elsebet Østergaard	24
9	Clinical and molecular analysis in families with autosomal recessive osteogenesis imperfecta identifies mutations in five genes and suggests genotype–phenotype correlations 2013 ·American Journal of Medical Genetics Part A ·José A. Caparrós‐Martín,Eulalia Valencia,Verónica Pulido,Víctor Martínez‐Glez,(unknown),Khalda Amr,Chantal Farra,Pablo Lapunzina,Víctor L. Ruiz‐Pérez,Samia A. Temtamy,Mona Aglan	46
10	Mutations in EOGT Confirm the Genetic Heterogeneity of Autosomal-Recessive Adams-Oliver Syndrome 2013 ·The American Journal of Human Genetics ·Ranad Shaheen,Mona Aglan,Kim M. Keppler‐Noreuil,Eissa Faqeih,Shinu Ansari,(unknown),Adel M. Ashour,Maha S. Zaki,Fatema Alzahrani,Anna M. Cueto‐González,Ghada M. H. Abdel‐Salam,Samia A. Temtamy,Fowzan S. Alkuraya	86
11	Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta 2010 ·The American Journal of Human Genetics ·Pablo Lapunzina,Mona Aglan,Samia A. Temtamy,José A. Caparrós‐Martín,Eulalia Valencia,Rocío Letón,Víctor Martínez‐Glez,(unknown),Khalda Amr,Nuria Vilaboa,Víctor L. Ruiz‐Pérez	205
12	Clinical, anthropometric, radiological and molecular characteristics of Egyptian achondroplasia patients 2009 ·Egyptian Journal of Medical Human Genetics ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Samia A. Temtamy	2
13	Genetic heterogeneity in spondylo-epimetaphyseal dysplasias: a clinical and radiological study 2007 ·Egyptian Journal of Medical Human Genetics ·Samia A. Temtamy,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	2
14	Transposition of external genitalia and associated malformations 2003 ·Clinical Dysmorphology ·Nagwa A. Meguid,Samia A. Temtamy,Inas Mazen	8
15	Familial Leydig Cell Hypoplasia as a Cause of Male Pseudohermaphroditism 1987 ·Human Heredity ·Mostafa K. El Awady,Samia A. Temtamy,(unknown),Yehia Z. Gad	22
16	A postaxial polydactyly-dental-vertebral syndrome 1977 ·The Journal of Pediatrics ·John Rogers,L. Stefan Levin,John P. Dorst,Samia A. Temtamy	7
17	The syndrome of aplasia cutis congenita with terminal, transverse defects of limbs 1975 ·The Journal of Pediatrics ·(unknown),Samia A. Temtamy	48
18	The Coffin-Lowry syndrome: An inherited faciodigital mental retardation syndrome 1975 ·The Journal of Pediatrics ·Samia A. Temtamy,Jordan Miller,(unknown)	66
19	Familial Turner phenotype 1969 ·The Journal of Pediatrics ·(unknown),Samia A. Temtamy	13
20	Carpenter's syndrome: Acrocephalopolysyndactyly. An autosomal recessive syndrome 1966 ·The Journal of Pediatrics ·Samia A. Temtamy	73

About Samia A. Temtamy

Samia A. Temtamy is a scholar working on Developmental Biology, Genetics and Rheumatology, having authored 127 papers that have together received 2.9k indexed citations. Recurring topics across this work include Connective tissue disorders research (25 papers), Congenital limb and hand anomalies (17 papers) and Genomic variations and chromosomal abnormalities (13 papers). The work is most often cited by research in Developmental Biology (209 citations), Genetics (1.6k citations) and Rheumatology (445 citations). Samia A. Temtamy has collaborated with scholars based in Egypt, United States and Spain. Frequent co-authors include Mona Aglan, Jordan Miller, Víctor L. Ruiz‐Pérez, Pablo Lapunzina, Eulalia Valencia, José A. Caparrós‐Martín, Víctor Martínez‐Glez, Nagwa A. Meguid, Khalda Amr and Ghada A. Otaify. Their work appears in journals such as Nature Genetics, The American Journal of Human Genetics and Human Molecular Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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