Samia A. Temtamy

6.7k total citations
127 papers, 2.9k citations indexed

About

Samia A. Temtamy is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Samia A. Temtamy has authored 127 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Genetics, 60 papers in Molecular Biology and 20 papers in Rheumatology. Recurrent topics in Samia A. Temtamy's work include Connective tissue disorders research (25 papers), Congenital limb and hand anomalies (17 papers) and Genomic variations and chromosomal abnormalities (13 papers). Samia A. Temtamy is often cited by papers focused on Connective tissue disorders research (25 papers), Congenital limb and hand anomalies (17 papers) and Genomic variations and chromosomal abnormalities (13 papers). Samia A. Temtamy collaborates with scholars based in Egypt, United States and Spain. Samia A. Temtamy's 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 and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Samia A. Temtamy

119 papers receiving 2.7k citations

Peers

Samia A. Temtamy

GENET

RHEUM

SURGE

PPCH

Peter Meinecke Germany

Charles I. Scott United States

Sigrid Tinschert Germany

I D Young United Kingdom

Andreas Winterpacht Germany

Ralph Lachman United States

Hirofumi Ohashi Japan

Leonard O. Langer United States

Sheila Unger Switzerland

R M Winter United Kingdom

Peter Meinecke Germany

Samia A. Temtamy

1.9k ×1.2

GENET

2.5k ×1.8

238 ×0.5

RHEUM

437 ×1.1

SURGE

274 ×1.0

PPCH

Citations per year, relative to Samia A. Temtamy Samia A. Temtamy (= 1×) peers Peter Meinecke

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

Kague, Érika, Francesco Turci, Kate Robson Brown, et al.. (2021). 3D assessment of intervertebral disc degeneration in zebrafish identifies changes in bone density that prime disc disease. Bone Research. 9(1). 39–39. 39 indexed citations

Horn, Denise, Julián Nevado, Nadja Ehmke, et al.. (2021). Biallelic truncating variants in MAPKAPK5 cause a new developmental disorder involving neurological, cardiac, and facial anomalies combined with synpolydactyly. Genetics in Medicine. 23(4). 679–688. 5 indexed citations

Besio, Roberta, Laura Leoni, Lina Cipolla, et al.. (2019). Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate. Disease Models & Mechanisms. 12(6). 52 indexed citations

Aglan, Mona, et al.. (2019). Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification. 8(2). 100. 1 indexed citations

Ismail, Somaia, et al.. (2018). ROBERTS SYNDROME: CLINICAL AND CYTOGENETIC STUDIES IN 8 EGYPTIAN PATIENTS AND MOLECULAR STUDIES IN 4 PATIENTS WITH GENOTYPE/PHENOTYPE CORRELATION.. PubMed. 27(3). 305–323. 4 indexed citations

Temtamy, Samia A., et al.. (2017). Genetics and Genomic Medicine in Egypt: steady pace. Molecular Genetics & Genomic Medicine. 5(1). 8–14. 7 indexed citations

Caparrós‐Martín, José A., Alessandro De Luca, François Cartault, et al.. (2015). 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. Human Molecular Genetics. 24(14). 4126–4137. 42 indexed citations

Valencia, Eulalia, José A. Caparrós‐Martín, Ma Salomé Sirerol-Piquer, et al.. (2014). Report of a newly indentified patient with mutations in BMP1 and underlying pathogenetic aspects. American Journal of Medical Genetics Part A. 164(5). 1143–1150. 24 indexed citations

Caparrós‐Martín, José A., Eulalia Valencia, Verónica Pulido, et al.. (2013). Clinical and molecular analysis in families with autosomal recessive osteogenesis imperfecta identifies mutations in five genes and suggests genotype–phenotype correlations. American Journal of Medical Genetics Part A. 161(6). 1354–1369. 46 indexed citations

10.

Shaheen, Ranad, Mona Aglan, Kim M. Keppler‐Noreuil, et al.. (2013). Mutations in EOGT Confirm the Genetic Heterogeneity of Autosomal-Recessive Adams-Oliver Syndrome. The American Journal of Human Genetics. 92(4). 598–604. 86 indexed citations

11.

Lapunzina, Pablo, Mona Aglan, Samia A. Temtamy, et al.. (2010). Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta. The American Journal of Human Genetics. 87(1). 110–114. 205 indexed citations

12.

Temtamy, Samia A., et al.. (2009). Clinical, anthropometric, radiological and molecular characteristics of Egyptian achondroplasia patients. Egyptian Journal of Medical Human Genetics. 10(1). 13–25. 2 indexed citations

13.

Temtamy, Samia A., et al.. (2007). Genetic heterogeneity in spondylo-epimetaphyseal dysplasias: a clinical and radiological study. Egyptian Journal of Medical Human Genetics. 8(2). 147–172. 2 indexed citations

14.

Meguid, Nagwa A., Samia A. Temtamy, & Inas Mazen. (2003). Transposition of external genitalia and associated malformations. Clinical Dysmorphology. 12(1). 59–62. 8 indexed citations

15.

Awady, Mostafa K. El, et al.. (1987). Familial Leydig Cell Hypoplasia as a Cause of Male Pseudohermaphroditism. Human Heredity. 37(1). 36–40. 22 indexed citations

16.

Rogers, John, L. Stefan Levin, John P. Dorst, & Samia A. Temtamy. (1977). A postaxial polydactyly-dental-vertebral syndrome. The Journal of Pediatrics. 90(2). 230–235. 7 indexed citations

17.

Temtamy, Samia A., et al.. (1975). The syndrome of aplasia cutis congenita with terminal, transverse defects of limbs. The Journal of Pediatrics. 87(1). 79–82. 48 indexed citations

18.

Temtamy, Samia A., et al.. (1975). The Coffin-Lowry syndrome: An inherited faciodigital mental retardation syndrome. The Journal of Pediatrics. 86(5). 724–731. 66 indexed citations

19.

Temtamy, Samia A., et al.. (1969). Familial Turner phenotype. The Journal of Pediatrics. 74(1). 67–72. 13 indexed citations

20.

Temtamy, Samia A.. (1966). Carpenter's syndrome: Acrocephalopolysyndactyly. An autosomal recessive syndrome. The Journal of Pediatrics. 69(1). 111–120. 73 indexed citations

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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