Shehla Mohammed

2.5k total citations
25 papers, 680 citations indexed

About

Shehla Mohammed is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Shehla Mohammed has authored 25 papers receiving a total of 680 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Shehla Mohammed's work include DNA Repair Mechanisms (3 papers), Mitochondrial Function and Pathology (3 papers) and RNA regulation and disease (3 papers). Shehla Mohammed is often cited by papers focused on DNA Repair Mechanisms (3 papers), Mitochondrial Function and Pathology (3 papers) and RNA regulation and disease (3 papers). Shehla Mohammed collaborates with scholars based in United Kingdom, Netherlands and France. Shehla Mohammed's co-authors include Kornelia Neveling, Daniela Endt, Marcel Freund, Ian Kesterton, Beatrice Schuster, Nazneen Rahman, Karen Barker, David Grimwade, Linda Hartmann and Roland G. Roberts and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and Brain.

In The Last Decade

Shehla Mohammed

25 papers receiving 655 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shehla Mohammed United Kingdom 12 497 248 92 76 61 25 680
Soo‐Mi Park United Kingdom 15 464 0.9× 258 1.0× 79 0.9× 39 0.5× 52 0.9× 39 794
Bryn D. Webb United States 13 588 1.2× 212 0.9× 60 0.7× 50 0.7× 34 0.6× 35 896
Pamela Magini Italy 16 347 0.7× 349 1.4× 119 1.3× 39 0.5× 45 0.7× 38 717
Nisha Patel Saudi Arabia 17 428 0.9× 267 1.1× 60 0.7× 28 0.4× 52 0.9× 39 727
Patricio Barros‐Núñez Mexico 15 359 0.7× 302 1.2× 54 0.6× 83 1.1× 26 0.4× 71 688
Gülen Eda Ütine Türkiye 14 367 0.7× 373 1.5× 28 0.3× 64 0.8× 52 0.9× 114 715
Makiko Meguro‐Horike Japan 14 477 1.0× 268 1.1× 88 1.0× 72 0.9× 36 0.6× 35 829
Maria Lisa Dentici Italy 19 704 1.4× 459 1.9× 44 0.5× 71 0.9× 63 1.0× 74 1.1k
J. Kunze Germany 14 328 0.7× 226 0.9× 72 0.8× 58 0.8× 61 1.0× 40 577

Countries citing papers authored by Shehla Mohammed

Since Specialization
Citations

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

Fields of papers citing papers by Shehla Mohammed

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shehla Mohammed

This figure shows the co-authorship network connecting the top 25 collaborators of Shehla Mohammed. A scholar is included among the top collaborators of Shehla Mohammed 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 Shehla Mohammed. Shehla Mohammed 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.
Nakazawa, Yuka, Yasuyoshi Oka, Hironobu Morinaga, et al.. (2025). TFIIH-p52ΔC defines a ninth xeroderma pigmentosum complementation–group XP-J and restores TFIIH stability to p8-defective trichothiodystrophy. Journal of Clinical Investigation. 135(22). 1 indexed citations
2.
Fassihi, Hiva, Shehla Mohammed, Yuka Nakazawa, et al.. (2025). XP-J, a ninth xeroderma pigmentosum complementation group, results from mutations in GTF2H4, encoding TFIIH-p52 subunit. Journal of Clinical Investigation. 135(22). 1 indexed citations
3.
Mantyh, William G., Christina A. Pacak, Paul D. Robbins, et al.. (2024). Cognitive Decline and Other Late-Stage Neurologic Complications in Cockayne Syndrome. Neurology Clinical Practice. 14(4). e200309–e200309. 2 indexed citations
4.
García‐Moreno, Héctor, Douglas R. Langbehn, Marta Manes, et al.. (2023). Neurological disease in xeroderma pigmentosum: prospective cohort study of its features and progression. Brain. 146(12). 5044–5059. 10 indexed citations
5.
Devito, Liani, Lyn Healy, Shehla Mohammed, François Guillemot, & Cristina Dias. (2021). Generation of an iPSC line (CRICKi001-A) from an individual with a germline SMARCA4 missense mutation and autism spectrum disorder. Stem Cell Research. 53. 102304–102304. 3 indexed citations
6.
Baer, Sarah, Peter B. Kang, Shehla Mohammed, et al.. (2020). Growth charts in Cockayne syndrome type 1 and type 2. European Journal of Medical Genetics. 64(1). 104105–104105. 8 indexed citations
7.
Beecroft, Sarah J., Josine M. de Winter, Coen A. C. Ottenheijm, et al.. (2019). Recessive MYH7-related myopathy in two families. Neuromuscular Disorders. 29(6). 456–467. 8 indexed citations
8.
Myers, Kenneth A., Susan M. White, Shehla Mohammed, et al.. (2018). Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome. Epilepsy Research. 140. 166–170. 13 indexed citations
9.
Marks, Seth D., Penny Fallon, Paul Johns, et al.. (2018). Parental mosaicism in RYR1-related Central Core Disease. Neuromuscular Disorders. 28(5). 422–426. 5 indexed citations
10.
Paolacci, Stefano, Débora Romeo Bertola, José Francisco da Silva Franco, et al.. (2017). Wiedemann–Rautenstrauch syndrome: A phenotype analysis. American Journal of Medical Genetics Part A. 173(7). 1763–1772. 27 indexed citations
11.
Parker, Michael, Alan Fryer, Deborah Shears, et al.. (2015). De novo, heterozygous, loss‐of‐function mutations in SYNGAP1 cause a syndromic form of intellectual disability. American Journal of Medical Genetics Part A. 167(10). 2231–2237. 79 indexed citations
12.
Cullup, Thomas, Carlo Dionisi‐Vici, Ay Lin Kho, et al.. (2013). Clinical utility gene card for: Vici Syndrome. European Journal of Human Genetics. 22(3). 435–435. 14 indexed citations
13.
Malhotra, Raman, et al.. (2013). Use of Dermal Filler to Improve Exposure Keratopathy in a Patient with Restrictive Dermopathy. Orbit. 32(1). 70–72. 3 indexed citations
14.
McClelland, Verity M., Thomas Cullup, István Bódi, et al.. (2010). Vici syndrome associated with sensorineural hearing loss and evidence of neuromuscular involvement on muscle biopsy. American Journal of Medical Genetics Part A. 152A(3). 741–747. 35 indexed citations
15.
Hanenberg, Helmut, Beatrice Schuster, Karen Barker, et al.. (2010). Mutation of the RAD51C gene in a Fanconi anemia–like disorder. Nature Genetics. 42(5). 406–409. 310 indexed citations
16.
Joseph, Sumy, S. Robb, Shehla Mohammed, et al.. (2009). Interfamilial phenotypic heterogeneity in SMARD1. Neuromuscular Disorders. 19(3). 193–195. 36 indexed citations
17.
Day, Richard O., Dian Donnai, Alan Fryer, et al.. (2008). A clinical and genetic study of the Say/Barber/Biesecker/Young‐Simpson type of Ohdo syndrome. Clinical Genetics. 74(5). 434–444. 17 indexed citations
18.
Seller, Mary J., Claudine Fear, Ajith Kumar, & Shehla Mohammed. (2004). Trisomy 16 in a mid-trimester IVF foetus with multiple abnormalities. Clinical Dysmorphology. 13(3). 187–189. 4 indexed citations
19.
Seller, Mary J., et al.. (2003). A trisomy 2 fetus with severe neural tube defects and other abnormalities. Clinical Dysmorphology. 13(1). 25–27. 25 indexed citations
20.
Seller, Mary J., et al.. (2002). Microdeletion 22q11.2, Kousseff syndrome and spina bifida. Clinical Dysmorphology. 11(2). 113–115. 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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