M. Sarfarazi

3.9k total citations
67 papers, 3.0k citations indexed

About

M. Sarfarazi is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, M. Sarfarazi has authored 67 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 19 papers in Genetics and 14 papers in Cellular and Molecular Neuroscience. Recurrent topics in M. Sarfarazi's work include Muscle Physiology and Disorders (13 papers), Genetic Neurodegenerative Diseases (12 papers) and Connective tissue disorders research (8 papers). M. Sarfarazi is often cited by papers focused on Muscle Physiology and Disorders (13 papers), Genetic Neurodegenerative Diseases (12 papers) and Connective tissue disorders research (8 papers). M. Sarfarazi collaborates with scholars based in United Kingdom, United States and Netherlands. M. Sarfarazi's co-authors include Peter S. Harper, I. Stoilov, John B. Schenkman, Marianne Jansson, P. Pearson, Kay E. Davies, Jeffrey Murray, R. Williamson, T O'Brien and Nick Thomas and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

M. Sarfarazi

67 papers receiving 2.9k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
M. Sarfarazi United Kingdom 28 1.7k 819 435 415 330 67 3.0k
Mary Dowd France 4 2.9k 1.7× 366 0.4× 370 0.9× 125 0.3× 300 0.9× 4 4.1k
L Kieckens Belgium 9 2.9k 1.7× 235 0.3× 402 0.9× 160 0.4× 271 0.8× 15 4.6k
Ivan B. Lobov United States 13 2.3k 1.4× 314 0.4× 254 0.6× 186 0.4× 134 0.4× 25 3.0k
Lyn Powell-Braxton United States 17 3.6k 2.1× 560 0.7× 480 1.1× 133 0.3× 194 0.6× 22 5.4k
Gwenaëlle Collod‐Béroud France 21 1.7k 1.0× 1.6k 2.0× 220 0.5× 114 0.3× 195 0.6× 38 3.6k
S. van Soest Netherlands 16 1.4k 0.8× 662 0.8× 188 0.4× 369 0.9× 55 0.2× 17 2.1k
Gianfranco Fenzi Italy 38 1.7k 1.0× 677 0.8× 136 0.3× 123 0.3× 86 0.3× 91 4.1k
An Zwijsen Belgium 35 3.4k 2.0× 454 0.6× 312 0.7× 56 0.1× 457 1.4× 87 4.7k
Andreas Winterpacht Germany 33 2.5k 1.4× 1.4k 1.7× 166 0.4× 62 0.1× 140 0.4× 85 3.7k
Sean F. Hackett United States 28 2.1k 1.2× 221 0.3× 256 0.6× 1.5k 3.6× 107 0.3× 54 3.2k

Countries citing papers authored by M. Sarfarazi

Since Specialization
Citations

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

Fields of papers citing papers by M. Sarfarazi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Sarfarazi

This figure shows the co-authorship network connecting the top 25 collaborators of M. Sarfarazi. A scholar is included among the top collaborators of M. Sarfarazi 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 M. Sarfarazi. M. Sarfarazi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Monemi, Sharareh, Anne H. Child, Ordan J. Lehmann, et al.. (2003). Genome Scan of Two Large Families with Adult-Onset Primary Open Angle Glaucoma (POAG) Suggests a Probable Locus on 5q33-q35. Investigative Ophthalmology & Visual Science. 44(13). 1128–1128. 3 indexed citations
2.
Jansson, Marianne, et al.. (2003). Comparative expression profiling of 40 mouse cytochrome P450 genes in embryonic and adult tissues. Archives of Biochemistry and Biophysics. 414(1). 91–100. 198 indexed citations
3.
Sarfarazi, M., I. Stoilov, & John B. Schenkman. (2003). Genetics and biochemistry of primary congenital glaucoma. Ophthalmology Clinics of North America. 16(4). 543–554. 84 indexed citations
4.
Stoilov, I. & M. Sarfarazi. (2002). The Third Genetic Locus (GLC3C) for Primary Congenital Glaucoma (PCG) Maps to Chromosome 14q24.3. Investigative Ophthalmology & Visual Science. 43(13). 3015–3015. 48 indexed citations
5.
Child, Anne H., et al.. (2002). Identification of an OPA1 truncating mutation in a family with Optic Atrophy. Investigative Ophthalmology & Visual Science. 43(13). 2393–2393. 1 indexed citations
6.
Brice, Glen, Sahar Mansour, R. Bryan Bell, et al.. (2002). Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24. Journal of Medical Genetics. 39(7). 478–483. 194 indexed citations
7.
Stoilov, I., Marianne Jansson, M. Sarfarazi, & John B. Schenkman. (2001). Roles of Cytochrome P450 in Development. Drug metabolism and drug interactions. 18(1). 33–56. 70 indexed citations
8.
Perçin, E. Ferda, Mustafa Kemal Arıcı, A.J. Rutherford, et al.. (2000). Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. Nature Genetics. 25(4). 397–401. 222 indexed citations
9.
Mangion, Jonathan, Nazneen Rahman, Sahar Mansour, et al.. (1999). A Gene for Lymphedema-Distichiasis Maps to 16q24.3. The American Journal of Human Genetics. 65(2). 427–432. 64 indexed citations
10.
Sarfarazi, M.. (1997). Recent advances in molecular genetics of glaucomas. Human Molecular Genetics. 6(10). 1667–1677. 138 indexed citations
11.
Bowcock, A., Robert I. Barnes, R. White, et al.. (1992). The CEPH consortium linkage map of human chromosome 15q. Genomics. 14(4). 833–840. 1 indexed citations
12.
Zonana, J., Angus Clarke, N S Thomas, et al.. (1988). Abstracts of the meeting of the Clinical Genetics Society. 20 and 21 November 1987, London. (Joint meeting with the Skeletal Dysplasia Group). Journal of Medical Genetics. 25(4). 274–283. 3 indexed citations
13.
Williams, Hywel, M. Sarfarazi, Christina Brown, Nick Thomas, & Peter S. Harper. (1986). The use of flanking markers in prediction for Duchenne muscular dystrophy.. Archives of Disease in Childhood. 61(3). 218–222. 17 indexed citations
14.
Sarfarazi, M. & Hywel Williams. (1986). A computer programme for estimation of genetic risk in X linked disorders, combining pedigree and DNA probe data with other conditional information.. Journal of Medical Genetics. 23(1). 40–45. 13 indexed citations
15.
Youngman, S, M. Sarfarazi, Oliver Quarrell, et al.. (1986). Studies of a DNA marker (G8) genetically linked to Huntington disease in British families. Human Genetics. 73(4). 333–339. 23 indexed citations
16.
Thomas, N S, Hywel Williams, Louis J. Elsas, et al.. (1986). Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome.. Journal of Medical Genetics. 23(6). 596–598. 36 indexed citations
17.
Harper, P.S. & M. Sarfarazi. (1985). Genetic prediction and family structure in Huntington's chorea.. BMJ. 290(6486). 1929–1931. 34 indexed citations
18.
Kingston, Helen, Nick Thomas, P. Pearson, M. Sarfarazi, & Peter S. Harper. (1983). Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.. Journal of Medical Genetics. 20(4). 255–258. 65 indexed citations
19.
Davies, Kay E., R. Williamson, Peter S. Harper, et al.. (1983). Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.. Journal of Medical Genetics. 20(4). 259–263. 60 indexed citations
20.
O'Brien, T, Peter S. Harper, Kay E. Davies, et al.. (1983). Absence of genetic heterogeneity in Duchenne muscular dystrophy shown by a linkage study using two cloned DNA sequences.. Journal of Medical Genetics. 20(4). 249–251. 10 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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