Shehla Mohammed

5.7k total citations
24 papers, 949 citations indexed

About

Shehla Mohammed is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Shehla Mohammed has authored 24 papers receiving a total of 949 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 15 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Shehla Mohammed's work include Genomic variations and chromosomal abnormalities (9 papers), BRCA gene mutations in cancer (7 papers) and Genetic Syndromes and Imprinting (4 papers). Shehla Mohammed is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), BRCA gene mutations in cancer (7 papers) and Genetic Syndromes and Imprinting (4 papers). Shehla Mohammed collaborates with scholars based in United Kingdom, United States and Belgium. Shehla Mohammed's co-authors include Nigel K. Spurr, Shirley Hodgson, C. MacGeoch, Caroline Mackie Ogilvie, D. Timothy Bishop, L. G. Bobrow, A M Hanby, D M Barnes, Bořivoj Vojtěšek and David P. Lane and has published in prestigious journals such as The Lancet, Journal of Clinical Investigation and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Shehla Mohammed

24 papers receiving 932 citations

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

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20 of 20 papers shown

#	Work	Indexed citations
1	The importance of psychological support for parents and caregivers of children with a rare disease at diagnosis 2022 ·Thomas Kenny, Kathleen R. Bogart, (unknown), (unknown), Susie M.D. Henley, (unknown), Shehla Mohammed, (unknown), (unknown), (unknown)	15
2	The Endocrine and Metabolic Characteristics of a Large Bardet-Biedl Syndrome Clinic Population 2018 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), Katharine F. Hunt, (unknown), Elizabeth Forsythe, Jonathan Hazlehurst, (unknown), Shehla Mohammed, Jeremy Tomlinson, Stephanie A. Amiel, Paul Carroll, (unknown), M. S. B. Huda, Barbara McGowan	67
3	Advances in Genetic Testing for Hereditary Cancer Syndromes 2016 ·Recent results in cancer research ·Ellen Thomas, Shehla Mohammed	4
4	Poly(A)-specific ribonuclease deficiency impacts telomere biology and causes dyskeratosis congenita 2015 ·Journal of Clinical Investigation ·Hemanth Tummala, Amanda J. Walne, Laura C. Collopy, Shirleny Cardoso, Josu de la Fuente, Sarah Lawson, James Powell, Nicola Cooper, Alison Foster, Shehla Mohammed, Vincent Plagnol, (unknown), Inderjeet Dokal	134
5	Cost Effectiveness of Using Array-CGH for Diagnosing Learning Disability 2015 ·Applied Health Economics and Health Policy ·Gurdeep S. Sagoo, Shehla Mohammed, (unknown), Gail Norbury, Joo Wook Ahn, Caroline Mackie Ogilvie, Mark Kroese	12
6	Genetic predictors of cardiovascular morbidity in Bardet–Biedl syndrome 2014 ·Clinical Genetics ·(unknown), (unknown), Bethan E. Hoskins, Emmanouil Bagkeris, Barbara McGowan, Paul Carroll, M. S. B. Huda, (unknown), Christopher J. Peters, Timothy Barrett, Shehla Mohammed, (unknown)	26
7	Clinical expression of Menkes disease in females with normal karyotype 2012 ·Orphanet Journal of Rare Diseases ·Lisbeth Birk Møller, Małgorzata Lenartowicz, M. T. Zabot, Josiane Arnaud, Lydie Bürglen, Chris Bennett, (unknown), Richard Fisher, Sandra Janssens, Shehla Mohammed, Margreet G.E.M. Ausems, Zeynep Tümer, Nina Horn, Thomas G. Jensen	36
8	17q24.2 microdeletions: a new syndromal entity with intellectual disability, truncal obesity, mood swings and hallucinations 2011 ·European Journal of Human Genetics ·Sarah Vergult, Andrew Dauber, Barbara Delle Chiaie, (unknown), Marleen Simon, Ali Rihani, Bart Loeys, Joel N. Hirschhorn, Jean P. Pfotenhauer, John A. Phillips, Shehla Mohammed, Caroline Mackie Ogilvie, John A. Crolla, Geert Mortier, Björn Menten	27
9	Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance 2010 ·Molecular Cytogenetics ·Joo Wook Ahn, Kathy Mann, (unknown), (unknown), (unknown), Zoe Docherty, Shehla Mohammed, Caroline Mackie Ogilvie	38
10	Segmental paternal uniparental disomy (patUPD) of 14q32 with abnormal methylation elicits the characteristic features of complete patUPD14 2010 ·American Journal of Medical Genetics Part A ·Melita Irving, Karin Buiting, Deniz Kanber, Celia Donaghue, Reiner Schulz, Amaka C Offiah, Shehla Mohammed, Rebecca J. Oakey	27
11	Detection of mosaicism for genome imbalance in a cohort of 3,042 clinical cases using an oligonucleotide array CGH platform 2010 ·European Journal of Medical Genetics ·(unknown), (unknown), Kathy Mann, (unknown), Sahar Mansour, Tessa Homfray, Shehla Mohammed, Caroline Mackie Ogilvie	32
12	Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment 2009 ·American Journal of Medical Genetics Part A ·Dianne F. Newbury, (unknown), (unknown), Elena Bacchelli, Simona Carone, Janine A. Lamb, Elena Maestrini, Emanuela V. Volpi, Shehla Mohammed, Gillian Baird, Anthony P. Monaco	19
13	Monozygotic twins discordant for frontonasal malformation 2004 ·American Journal of Medical Genetics Part A ·Shehla Mohammed, Marc C. Swan, Steven A. Wall, Andrew O.M. Wilkie	13
14	Detection of submicroscopic subtelomeric chromosome translocations: A new case study 2000 ·American Journal of Medical Genetics ·(unknown), Shehla Mohammed, Caroline Mackie Ogilvie	14
15	Identification of missense and truncating mutations in the BRCA1 gene in sporadic and familial breast and ovarian cancer 1998 ·Genes Chromosomes and Cancer ·(unknown), Shehla Mohammed, David Ellis, Sally Watts, (unknown), Louise Izatt, Diana M. Barnes, Ellen Solomon, Shirley Hodgson, Christopher G. Mathew	25
16	Mutations and alternative splicing of the BRCA1 gene in UK breast/ovarian cancer families 1997 ·Genes Chromosomes and Cancer ·Chun‐Fang Xu, Julie A. Chambers, H Nicolai, Melissa A. Brown, (unknown), Shehla Mohammed, Shirley Hodgson, David P. Kelsell, Nigel K. Spurr, D. Timothy Bishop, Ellen Solomon	9
17	Mutations and alternative splicing of the BRCA1 gene in UK breast/ovarian cancer families. 1997 ·PubMed ·Chun‐Fang Xu, Julie A. Chambers, H Nicolai, Myles Brown, (unknown), Shehla Mohammed, Shirley Hodgson, David P. Kelsell, Nigel K. Spurr, D. Timothy Bishop, E. Solomon	64
18	A possible screening test for inherited p53-related defects based on the apoptotic response of peripheral blood lymphocytes to DNA damage 1995 ·British Journal of Cancer ·RS Camplejohn, J. Jefferson P. Perry, SV Hodgson, G. S. Turner, Ann C. Williams, Carol Upton, C. MacGeoch, Shehla Mohammed, DM Barnes	32
19	p53 Protein Detected By Immunohistochemical Staining is Not Always Mutant 1993 ·Disease Markers ·C. MacGeoch, Diana M. Barnes, Julia A. Newton, Shehla Mohammed, Shirley V. Hodgson, Mun Hon Ng, D. Timothy Bishop, Nigel K. Spurr	45
20	Abnormal expression of wild type p53 protein in normal cells of a cancer family patient 1992 ·The Lancet ·D M Barnes, C E Gillett, L. G. Bobrow, A M Hanby, Shehla Mohammed, Shirley Hodgson, Irene M. Leigh, (unknown), C. MacGeoch, Nigel K. Spurr, Jiří Bártek, Bořivoj Vojtěšek, Steven M. Picksley, David P. Lane	170

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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