Lily Islam

2.2k total citations
14 papers, 304 citations indexed

About

Lily Islam is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Lily Islam has authored 14 papers receiving a total of 304 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Lily Islam's work include Ocular Disorders and Treatments (4 papers), Genetic Syndromes and Imprinting (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). Lily Islam is often cited by papers focused on Ocular Disorders and Treatments (4 papers), Genetic Syndromes and Imprinting (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). Lily Islam collaborates with scholars based in United Kingdom, France and Netherlands. Lily Islam's co-authors include Jane C. Sowden, Daniel Kelberman, Ken K. Nischal, Paul O’Donnell, Adrienne M. Flanagan, Thomas S. Jacques, Els V. Meulemans, Guido M.J.M. Roemen, Maria Fernanda Amary and Patrick Pauwels and has published in prestigious journals such as Ophthalmology, Human Molecular Genetics and Gene.

In The Last Decade

Lily Islam

13 papers receiving 302 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lily Islam United Kingdom	9	113	110	83	61	47	14	304
Marc Putterman France	12	62 0.5×	52 0.5×	49 0.6×	97 1.6×	68 1.4×	26	325
José Luis Tovilla-Canales Mexico	9	36 0.3×	41 0.4×	56 0.7×	67 1.1×	41 0.9×	22	303
Yassir Abou-Rayyah United Kingdom	9	25 0.2×	64 0.6×	91 1.1×	130 2.1×	67 1.4×	13	390
Daniela Moncini Italy	10	29 0.3×	50 0.5×	56 0.7×	48 0.8×	9 0.2×	30	353
Emily Ceisler United States	11	55 0.5×	60 0.5×	25 0.3×	223 3.7×	51 1.1×	17	409
N Ducrey Switzerland	9	42 0.4×	151 1.4×	77 0.9×	52 0.9×	68 1.4×	43	441
Anthony Vandersteen United Kingdom	11	79 0.7×	152 1.4×	355 4.3×	60 1.0×	18 0.4×	21	448
Charles Zarnitsky France	8	190 1.7×	72 0.7×	46 0.6×	151 2.5×	25 0.5×	19	463
Ignazio Maria Vallone Italy	12	20 0.2×	44 0.4×	23 0.3×	100 1.6×	51 1.1×	23	368
Illuminato Carosi Italy	9	35 0.3×	30 0.3×	20 0.2×	58 1.0×	32 0.7×	22	309

Countries citing papers authored by Lily Islam

Since Specialization

Citations

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

Fields of papers citing papers by Lily Islam

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lily Islam

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

All Works

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14 of 14 papers shown

Peter, Michelle, et al.. (2025). ‘I Have my Beliefs, but Then I Have my Reality’: Reflections of Black and South Asian Parents Living in England on Screening and Genetic Diagnosis in Pregnancy. Prenatal Diagnosis. 45(7). 857–866. 1 indexed citations

Black, Georgia, Judith Yargawa, Cecilia Vindrola‐Padros, et al.. (2025). South Asian patient experiences of professional interpreting service provision in general practice in England: a qualitative interview study. International Journal for Equity in Health. 24(1). 104–104.

Williams, Emily D., Paramjit Gill, Georgia Black, et al.. (2024). Uptake and experience of professional interpreting services in primary care in a South Asian population: a national cross-sectional study. BMC Primary Care. 25(1). 405–405. 1 indexed citations

McDermott, Helen, et al.. (2023). Paediatric survivors beyond infancy with Stüve-Wiedemann syndrome – A case series from the West Midlands, UK. European Journal of Medical Genetics. 66(8). 104788–104788. 1 indexed citations

Choong, Andrew M.T.L., Natalie Canham, Sophie Renton, et al.. (2015). A combined vascular surgical and clinical genetics approach to diffuse aneurysmal disease. Annals of The Royal College of Surgeons of England. 97(5). e73–e76. 3 indexed citations

Kelberman, Daniel, Lily Islam, Jörn Lakowski, et al.. (2014). Mutation of SALL2 causes recessive ocular coloboma in humans and mice. Human Molecular Genetics. 23(10). 2511–2526. 37 indexed citations

Islam, Lily, Daniel Kelberman, Laura Williamson, et al.. (2014). Functional Analysis ofFOXE3Mutations Causing Dominant and Recessive Ocular Anterior Segment Disease. Human Mutation. 36(3). 296–300. 17 indexed citations

Kelberman, Daniel, Renata S. Auriemma, Suzanne Drury, et al.. (2013). A novel heterozygous SOX2 mutation causing congenital bilateral anophthalmia, hypogonadotropic hypogonadism and growth hormone deficiency. Gene. 534(2). 282–285. 20 indexed citations

Kelberman, Daniel, Lily Islam, Thomas S. Jacques, et al.. (2011). CYP1B1-Related Anterior Segment Developmental Anomalies. Ophthalmology. 118(9). 1865–1873. 16 indexed citations

10.

Kelberman, Daniel, Lily Islam, Susan Holder, et al.. (2011). Digenic inheritance of mutations in FOXC1 and PITX2 : Correlating transcription factor function and axenfeld-rieger disease severity. Human Mutation. 32(10). 1144–1152. 28 indexed citations

11.

Vogt, Julie, Neil V. Morgan, Laurence Bonhomme‐Faivre, et al.. (2011). CHRNG genotype–phenotype correlations in the multiple pterygium syndromes. Journal of Medical Genetics. 49(1). 21–26. 30 indexed citations

12.

Mataftsi, Asimina, Lily Islam, Daniel Kelberman, Jane C. Sowden, & Ken K. Nischal. (2011). Chromosome abnormalities and the genetics of congenital corneal opacification.. PubMed. 17. 1624–40. 25 indexed citations

13.

Gikas, Panagiotis D., Lily Islam, William Aston, et al.. (2009). Nonbacterial osteitis: a clinical, histopathological, and imaging study with a proposal for protocol-based management of patients with this diagnosis. Journal of Orthopaedic Science. 14(5). 505–516. 52 indexed citations

14.

Amary, Maria Fernanda, Patrick Pauwels, Els V. Meulemans, et al.. (2007). Detection of β-Catenin Mutations in Paraffin-embedded Sporadic Desmoid-type Fibromatosis by Mutation-specific Restriction Enzyme Digestion (MSRED): an Ancillary Diagnostic Tool. The American Journal of Surgical Pathology. 31(9). 1299–1309. 73 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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