Solaf M. Elsayed

1.9k citations

63 papers · 1.1k indexed · h-index 15

Impact in

Genetics top 5%
- Connective tissue disorders research
- Genetic and Kidney Cyst Diseases
- Genetics and Neurodevelopmental Disorders
Sensory Systems top 10%

Papers in ⓘ

Molecular Biology 23
- Mitochondrial Function and Pathology 4
- DNA Repair Mechanisms 3
Genetics 14
- Connective tissue disorders research 4
- Genetic and Kidney Cyst Diseases 3

Co-authors: Rabah M. Shawky (14 shared papers)Ezzat Elsobky (15 shared papers)Moushira Zaki (1 shared paper)David M. Yousem (1 shared paper)Bart Loeys (1 shared paper)Ghada M. El‐Sayed (2 shared papers)Hal Dietz (1 shared paper)Joshua D. Smith (1 shared paper)
Journals: Orphanet Journal of Rare Diseases (3 papers)QJM (2 papers)Pediatric Neurology (2 papers)European Journal of Human Genetics (1 paper)Genetics in Medicine (1 paper)
Partner nations: Egypt Germany Türkiye

In The Last Decade

Solaf M. Elsayed

57 papers receiving 1.1k citations

Peers

Countries citing papers authored by Solaf M. Elsayed

Since Specialization

Citations

This map shows the geographic impact of Solaf M. Elsayed'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 Solaf M. Elsayed with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Solaf M. Elsayed more than expected).

Fields of papers citing papers by Solaf M. Elsayed

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Solaf M. Elsayed. 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 Solaf M. Elsayed. The network helps show where Solaf M. Elsayed may publish in the future.

Co-authors

The 25 scholars most cited alongside Solaf M. Elsayed, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Solaf M. Elsayed Line = papers co-authored together Solaf M. Elsayed links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 63 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta The American Journal of Human Genetics ·Shawna M. Pyott, Thao Tran, Dru F. Leistritz, Melanie Pepin, Nancy J. Mendelsohn, Renee Temme, Bridget A. Fernandez, Solaf M. Elsayed, Ezzat Elsobky, I. C. Verma, Sreelata Nair, Emily H. Turner, Joshua D. Smith, Gail P. Jarvik, Peter H. Byers	2013	170
2	Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics Journal of Clinical Investigation ·Claudia Dafinger, Max C. Liebau, Solaf M. Elsayed, Yorck Hellenbroich, Eugen Boltshauser, Georg Christoph Korenke, Francesca Fabretti, Andreas Janecke, Inga Ebermann, Gudrun Nürnberg, Peter Nürnberg, Hanswalter Zentgraf, Friederike Koerber, Klaus Addicks, Ezzat Elsobky, Thomas Benzing, Bernhard Schermer, Hanno J. Bolz	2011	141
3	The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care Genetics in Medicine ·Brian T. Wilson, Zornitza Stark, Ruth E. Sutton, Sumita Danda, Alka V. Ekbote, Solaf M. Elsayed, Louise Gibson, Judith A. Goodship, Andrew P. Jackson, Wee ik Te Keng, Mary D. King, Emma McCann, Toshino Motojima, J. Elliot Murray, Taku Omata, Daniela T. Pilz, Kate Pope, Katsuo Sugita, Susan M. White, Ian Wilson	2015	108
4	Consanguinity and its relevance to clinical genetics Egyptian Journal of Medical Human Genetics ·Rabah M. Shawky, Solaf M. Elsayed, Moushira Zaki, Sahar M. Nour El-Din, Ferihan M. Kamal	2013	91
5	Consanguineous matings among Egyptian population Egyptian Journal of Medical Human Genetics ·Rabah M. Shawky, Mohammed Y. El-Awady, Solaf M. Elsayed, Ghada E. Hamadan	2011	89
6	Neuroradiologic Manifestations of Loeys-Dietz Syndrome Type 1 American Journal of Neuroradiology ·V J Rodrigues, Solaf M. Elsayed, Bart Loeys, Hal Dietz, David M. Yousem	2009	75
7	Evidence for single origins of 35delG and delE120 mutations in the GJB2 gene in Anatolia Clinical Genetics ·Mustafa Tekin, G Boğoçlu, S. T. Arican, MN Orman, Hakkı Taştan, Solaf M. Elsayed, Nejat Akar	2004	49
8	Phenotypic and Genetic Characterization of a Cohort of Pediatric Wilson Disease Patients BMC Pediatrics ·Tawhida Y. Abdel Ghaffar, Solaf M. Elsayed, Suzan El‐Naghy, Ahmed Shadeed, Ezzat Elsobky, H Schmidt	2011	43
9	Clinical and genetic characterization of chanarin-dorfman syndrome patients: first report of large deletions in the ABHD5 gene Orphanet Journal of Rare Diseases ·Chiara Redaelli, Rosalind Coleman, Laura Moro, Catherine Dacou‐Voutetakis, Solaf M. Elsayed, Daniele Prati, Agostino Colli, Donatella Mela, Roberto Colombo, Daniela Tavian	2010	40
10	Mutational analysis of ATP7B gene in Egyptian children with Wilson disease: 12 novel mutations Journal of Human Genetics ·Tawhida Yassin Abdel-Ghaffar, Solaf M. Elsayed, Ezzat Elsobky, Bettina Bochow, Janine Büttner, Hartmut Schmidt	2008	33
11	Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations European Journal of Human Genetics ·Solaf M. Elsayed, Raoul Heller, Michaela Thoenes, Maha S. Zaki, Daniel Swan, Ezzat Elsobky, Christine Zühlke, Inga Ebermann, Gudrun Nürnberg, Peter Nürnberg, Hanno J. Bolz	2013	28
12	Phenotype of apoptotic lymphocytes in children with Down syndrome Immunity & Ageing ·Solaf M. Elsayed, Ghada M. El‐Sayed	2009	23
13	Outcome of enzyme replacement therapy in children with Gaucher disease: The Egyptian experience Egyptian Journal of Medical Human Genetics ·Ahmed S. Khalifa, Azza Abdel Gawad Tantawy, Rabah M. Shawky, Eman Monir, Solaf M. Elsayed, Ekram Fateen, Alan Cooper	2011	21
14	Structural chromosomal abnormalities in couples with recurrent abortion in Egypt TURKISH JOURNAL OF MEDICAL SCIENCES ·Nagwa E. A. Gaboon, Ahmed Ramy MOHAMED, Solaf M. Elsayed, Osama K. Zaki, Mohamed A. Zayed	2015	19
15	Frequency of five thrombophilic polymorphisms in the Egyptian population. PubMed ·Arzu Ulu, Ezzat Elsobky, Solaf M. Elsayed, Züleyha Yıldız, Mustafa Tekin, Nejat Akar	2006	18
16	Maladaptative Autophagy Impairs Adipose Function in Congenital Generalized Lipodystrophy due to Cavin-1 Deficiency The Journal of Clinical Endocrinology & Metabolism ·Laurence Salle-Teyssières, Martine Auclair, Faraj Terro, Mona Nemani, Solaf M. Elsayed, Ezzat Elsobky, Mark Lathrop, Marc Délepine, Olivier Lascols, Jacqueline Capeau, Jocelyne Magré, Corinne Vigouroux	2016	13
17	Treatment options for patients with Gaucher disease Egyptian Journal of Medical Human Genetics ·Rabah M. Shawky, Solaf M. Elsayed	2016	13
18	Orthopaedic manifestations of Proteus syndrome in a child with literature update Bone Reports ·Tamer A. El-Sobky, Solaf M. Elsayed, Dalia M. E. El Mikkawy	2015	11
19	A case of infantile osteopetrosis: The radioclinical features with literature update Bone Reports ·Tamer A. El-Sobky, Ezzat Elsobky, Ismaiel Sadek, Solaf M. Elsayed, Mohamed Fawzy Khattab	2015	11
20	Role of Plasma Amino Acids and Urinary Organic Acids in Diagnosis of Mitochondrial Diseases in Children Pediatric Neurology ·Hamed M. Shatla, Hoda Tomoum, Solaf M. Elsayed, Iman A. Elagouza, Rania Shatla, Mostafa M. Mohsen, Ashraf Hamed	2014	11

About Solaf M. Elsayed

Solaf M. Elsayed is a scholar working on Molecular Biology, Genetics, Hematology, Rheumatology and Physiology, having authored 63 papers that have together received 1.1k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (7 papers), Lysosomal Storage Disorders Research (5 papers), Blood Coagulation and Thrombosis Mechanisms (4 papers), Mitochondrial Function and Pathology (4 papers), Connective tissue disorders research (4 papers), Autoimmune and Inflammatory Disorders Research (4 papers), Genetic and Kidney Cyst Diseases (3 papers) and DNA Repair Mechanisms (3 papers). The work is most often cited by research in Genetics (471 citations), Sensory Systems (49 citations), Rheumatology (146 citations), Hematology (100 citations) and Genetics (85 citations). Solaf M. Elsayed has collaborated with scholars based in Egypt, Germany and Türkiye. Frequent co-authors include Rabah M. Shawky, Ezzat Elsobky, Moushira Zaki, David M. Yousem, Bart Loeys, Ghada M. El‐Sayed, Hal Dietz, Joshua D. Smith, Emily H. Turner and Thao Tran. Their work appears in journals such as Orphanet Journal of Rare Diseases, QJM, Pediatric Neurology, European Journal of Human Genetics and Genetics in Medicine.

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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