Shehla Mohammed

3.4k total citations · 1 hit paper
7 papers, 2.4k citations indexed

About

Shehla Mohammed is a scholar working on Molecular Biology, Immunology and Endocrine and Autonomic Systems. According to data from OpenAlex, Shehla Mohammed has authored 7 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 2 papers in Immunology and 1 paper in Endocrine and Autonomic Systems. Recurrent topics in Shehla Mohammed's work include RNA modifications and cancer (2 papers), Mitochondrial Function and Pathology (2 papers) and RNA Research and Splicing (2 papers). Shehla Mohammed is often cited by papers focused on RNA modifications and cancer (2 papers), Mitochondrial Function and Pathology (2 papers) and RNA Research and Splicing (2 papers). Shehla Mohammed collaborates with scholars based in United Kingdom, France and Spain. Shehla Mohammed's co-authors include Maria A. Soos, Johannes B. Prins, Jane A. Hurst, Ciaran Sewter, Elizabeth Montague, Anthony Barnett, I. Sadaf Farooqi, Nicholas J. Wareham, Janet E. Digby and Harald Rau and has published in prestigious journals such as Nature, British Journal of Dermatology and Metabolism.

In The Last Decade

Shehla Mohammed

7 papers receiving 2.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Congenital leptin deficiency is associated with severe early-onset obesity in humans

1997 2.2k citations Elizabeth Montague, I. Sadaf Farooqi et al. Nature profile →

Peers

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

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

#	Work	Indexed citations
1	Exome sequencing reveals a de novo POLD1 mutation causing phenotypic variability in mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome (MDPL) 2017 ·Metabolism ·Sahar Elouej, Ana Beleza‐Meireles, Richard Caswell, Kevin Colclough, Sian Ellard, Jean‐Pierre Desvignes, Christophe Béroud, Nicolas Lévy, Shehla Mohammed, Annachiara De Sandre‐Giovannoli	37
2	An isolated case of lissencephaly caused by the insertion of a mitochondrial genome-derived DNA sequence into the 5' untranslated region of the PAFAH1B1 (LIS1) gene 2010 ·Human Genomics ·David Millar, Carolyn Tysoe, L. Lazarou, Daniela T. Pilz, Shehla Mohammed, (unknown), Nadia Chuzhanova, D.N. Cooper, Rachel Butler	9
3	Hutchinson–Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature 2007 ·British Journal of Dermatology ·J. Mazereeuw‐Hautier, Louise C. Wilson, Shehla Mohammed, Dawn T. Smallwood, Sue Shackleton, David J. Atherton, John Harper	29
4	Fourteen novel OPA1 mutations in autosomal dominant optic atrophy including two de novo mutations in sporadic optic atrophy 2003 ·Human Mutation ·Olivier R. Baris, Cécile Delettre, Patrizia Amati‐Bonneau, (unknown), (unknown), (unknown), (unknown), (unknown), Hélène Dollfus, Philippe Jonveaux, Carmen Ayuso, Irene H. Maumenee, Birgit Lorenz, Shehla Mohammed, Yves Tourmen, Dominique Bonneau, Yves Malthièry, Christian Hamel, Pascal Reynier	50
5	Peroxisomal disorders: Clinical and biochemical studies in 15 children and prenatal diagnosis in 7 families 1999 ·American Journal of Medical Genetics ·Steven J. Steinberg, (unknown), (unknown), (unknown), Nicholas R. Dennis, Shehla Mohammed, Anthony H. Fensom	11
6	Congenital leptin deficiency is associated with severe early-onset obesity in humans breakdown → 1997 ·Nature ·Elizabeth Montague, I. Sadaf Farooqi, Jonathan P. Whitehead, Maria A. Soos, Harald Rau, Nicholas J. Wareham, Ciaran Sewter, Janet E. Digby, Shehla Mohammed, Jane A. Hurst, (unknown), (unknown), Anthony Barnett, Johannes B. Prins, Stephen O’Rahilly	2182
7	Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy? 1994 ·Journal of Medical Genetics ·Charis Eng, Victoria Murday, S. Seal, Shehla Mohammed, S V Hodgson, M.A. Chaudary, I S Fentiman, B. A. J. Ponder, Rosalind A. Eeles	74

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.

Explore authors with similar magnitude of impact