Nazneen Rahman

74.9k citations

120 papers · 12.8k indexed · 6 hit papers · h-index 53

Molecular Biology top 0.5%
Genetics top 0.05%
Cancer Research top 0.2%
Oncology top 1%
Pathology and Forensic Medicine top 0.5%

Co-authors: Michael R. Stratton P. Andrew Futreal Richard Wooster Lachlan Coin Tim Hubbard Thomas A. Down Mhairi Marshall Rita Barfoot
Topics: BRCA gene mutations in cancer (38 papers)Genetic factors in colorectal cancer (20 papers)DNA Repair Mechanisms (18 papers)
Cited by: Cancer Research Genetics Molecular Biology
Journals: Nature New England Journal of Medicine Proceedings of the National Academy of Sciences
Partner nations: United Kingdom United States Netherlands

In The Last Decade

Nazneen Rahman

115 papers receiving 12.5k citations

Hit Papers

5 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.

A census of human cancer genes

2004 2.2k citations P. Andrew Futreal, Nazneen Rahman et al. profile →
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

2006 689 citations Nazneen Rahman, Sheila Seal et al. Nature Genetics profile →
Prevalence of BRCA1 and BRCA2 Gene Mutations in Patients With Early-Onset Breast Cancer

1999 662 citations Rita Barfoot, S. Seal et al. profile →
Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk

2015 579 citations Douglas F. Easton, Paul D.P. Pharoah et al. New England Journal of Medicine profile →
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

2006 513 citations Sheila Seal, Patrick Kelly et al. Nature Genetics profile →
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles

2006 511 citations Sheila Seal, Patrick Kelly et al. Nature Genetics profile →

Peers

Countries citing papers authored by Nazneen Rahman

Since Specialization

Citations

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

Fields of papers citing papers by Nazneen Rahman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nazneen Rahman

This figure shows the co-authorship network connecting the top 25 collaborators of Nazneen Rahman. A scholar is included among the top collaborators of Nazneen Rahman 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 Nazneen Rahman. Nazneen Rahman 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:

20 of 20 papers shown

#	Work	Indexed citations
1	MCF classifier: Estimating, standardizing, and stratifying medicine carbon footprints, at scale 2024 ·British Journal of Clinical Pharmacology ·H. A. Taylor,Shazia Mahamdallie,M. H. Sawyer,Nazneen Rahman	1
2	Chromosomal instability by mutations in the novel minor spliceosome component CENATAC 2021 ·The EMBO Journal ·(unknown),Ali Oghabian,Maureen V. Akinyi,Sandra Hanks,Eelco C. Tromer,Jolien J. E. van Hooff,Lisa van Voorthuijsen,(unknown),(unknown),Esther C. H. Uijttewaal,Marijke Baltissen,Shawn Yost,(unknown),Michiel Vermeulen,‎Berend Snel,(unknown),Nazneen Rahman,Mikko J. Frilander,Geert J.P.L. Kops	27
3	Oncologist-led BRCA ‘mainstreaming’ in the ovarian cancer clinic: A study of 255 patients and its impact on their management 2020 ·Scientific Reports ·(unknown),Mark P. Lythgoe,Iain A. McNeish,Hani Gabra,Laura A. Tookman,Nazneen Rahman,Angela George,Jonathan Krell	40
4	Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma 2017 ·PLoS Genetics ·Lee McDaniel,Karina L. Conkrite,Xiao Chang,Mario Capasso,Zalman Vaksman,Derek A. Oldridge,Anna Zachariou,(unknown),Maura Diamond,Cuiping Hou,Achille Iolascon,Håkon Håkonarson,Nazneen Rahman,Marcella Devoto,Sharon J. Diskin	63
5	A cost analysis of a cancer genetic service model in the UK 2016 ·Journal of Community Genetics ·(unknown),Ingrid Slade,Helen Hanson,Angela George,Kelly Kohut,Ann Strydom,Sarah Wordsworth,Nazneen Rahman	29
6	Gene-Panel Sequencing and the Prediction of Breast-Cancer Riskbreakdown → 2015 ·New England Journal of Medicine ·Douglas F. Easton,Paul D.P. Pharoah,Antonis C. Antoniou,Marc Tischkowitz,Sean V. Tavtigian,Katherine L. Nathanson,Peter Devilee,Alfons Meindl,Fergus J. Couch,Melissa C. Southey,David E. Goldgar,D. Gareth Evans,Georgia Chenevix‐Trench,Nazneen Rahman,Mark E. Robson,Susan M. Domchek,William D. Foulkes	579
7	Recognition of and Response to neonatal intrapartum-related complications in home-birth settings in Bangladesh. 2014 ·PubMed ·Kristin VanderEnde,Allisyn C. Moran,(unknown),Louise T. Day,Kaosar Afsana,Nahid Kalim,(unknown),Nazneen Rahman,(unknown),(unknown),Lynn Sibley	0
8	BRCA1 testing should be offered to individuals with triple-negative breast cancer diagnosed below 50 years 2012 ·British Journal of Cancer ·(unknown),Lindsay B. Robertson,Helen Hanson,S. Seal,Margaret Warren-Perry,Deborah Hughes,Imran Howell,Clare Turnbull,Richard S. Houlston,Susan Shanley,Stephen A. Butler,D. Gareth Evans,Gill Ross,Diana Eccles,Andrew Tutt,Nazneen Rahman	79
9	Molecular Causes for BUBR1 Dysfunction in the Human Cancer Predisposition Syndrome Mosaic Variegated Aneuploidy 2010 ·Cancer Research ·Saskia J.E. Suijkerbuijk,Maria H.J. van Osch,Frank L. Bos,Sandra Hanks,Nazneen Rahman,Geert J.P.L. Kops	96
10	Estrogen Receptor Status Could Modulate the Genomic Pattern in Familial and Sporadic Breast Cancer 2007 ·Clinical Cancer Research ·Lorenzo Melchor,Emiliano Honrado,Jia Huang,Sara Álvarez,Tara L. Naylor,María J. García,Ana Osório,David Blesa,Michael R. Stratton,Barbara Weber,Juan C. Cigudosa,Nazneen Rahman,Katherine L. Nathanson,Javier Benı́tez	28
11	Cancer genes associated with phenotypes in monoallelic and biallelic mutation carriers: new lessons from old players 2007 ·Human Molecular Genetics ·Nazneen Rahman,(unknown)	56
12	The emerging landscape of breast cancer susceptibility 2007 ·Nature Genetics ·Michael R. Stratton,Nazneen Rahman	341
13	Biallelic mutations in PALB2 cause Fanconi anemia and predispose to childhood cancer 2007 ·Cancer Research ·Sarah Reid,Detlev Schindler,Helmut Hanenberg,Marc Tischkowitz,Sandra Hanks,Karen Barker,Patrick Kelly,Sheila Seal,Sat Dev Batish,Francis P. Lach,Reinhard Kalb,Kornelia Neveling,Christopher G. Mathew,Arleen D. Auerbach,Nazneen Rahman	1
14	Sotos syndrome 2006 ·European Journal of Human Genetics ·Katrina Tatton‐Brown,Nazneen Rahman	101
15	Familial gigantism caused by an NSD1 mutation 2005 ·American Journal of Medical Genetics Part A ·Mieke M. van Haelst,(unknown),Geneviève Baujat,Hennie T. Brüggenwirth,Ingrid M.B.H. van de Laar,Kim Coleman,Nazneen Rahman,Martinus F. Niermeijer,S L S Drop,Peter Scambler	17
16	Confirmation of a hereditary motor and sensory neuropathy IIC locus at chromosome 12q23‐q24 2005 ·Annals of Neurology ·Meriel McEntagart,(unknown),(unknown),Jenny Douglas,(unknown),(unknown),Neil E. Anderson,Nazneen Rahman	21
17	Ehlers-Danlos Syndrome with Severe Early-Onset Periodontal Disease (EDS-VIII) Is a Distinct, Heterogeneous Disorder with One Predisposition Gene at Chromosome 12p13 2003 ·The American Journal of Human Genetics ·Nazneen Rahman,Melanie Dunstan,M. Dawn Teare,Sandra Hanks,Jenny Douglas,Kim Coleman,(unknown),Mary Ellen Campbell,Britta Berglund,Magnus Nordenskjöld,(unknown),Nigel Burrows,Peter Lunt,Ian Young,Nigel Williams,Graham R. Bignell,P. Andrew Futreal,F M Pope	38
18	The Gene for Juvenile Hyaline Fibromatosis Maps to Chromosome 4q21 2002 ·The American Journal of Human Genetics ·Nazneen Rahman,Melanie Dunstan,M. Dawn Teare,Sandra Hanks,Sarah Edkins,Jaime Hughes,Graham R. Bignell,Grazia M.S. Mancini,Wim J. Kleijer,Mary Ellen Campbell,(unknown),Carol M. Black,Nigel Williams,Laura Arbour,Matthew L. Warman,Andrea Superti‐Furga,P. Andrew Futreal,F. Michael Pope	58
19	Confirmation of a gene locus for medullary cystic kidney disease (MCKD2) on chromosome 16p12 2001 ·Kidney International ·Nick Hateboer,Curtis Gumbs,M. Dawn Teare,(unknown),David Griffiths,David Ravine,PA Futreal,Nazneen Rahman	17
20	The Gene for Cherubism Maps to Chromosome 4p16.3 1999 ·The American Journal of Human Genetics ·(unknown),Nazneen Rahman,Sarah Edkins,Rita Barfoot,Trang Thi Thu Nguyen,Ásgeir Sigurðsson,John Townend,David Fitzpatrick,Adrienne M. Flanagan,Michael R. Stratton	115

About Nazneen Rahman

Nazneen Rahman is a scholar working on Genetics, Cancer Research and Pathology and Forensic Medicine, having authored 120 papers that have together received 12.8k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (38 papers), Genetic factors in colorectal cancer (20 papers) and DNA Repair Mechanisms (18 papers). The work is most often cited by research in Cancer Research (3.5k citations), Genetics (6.4k citations) and Molecular Biology (8.0k citations). Nazneen Rahman has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Michael R. Stratton, P. Andrew Futreal, Richard Wooster, Lachlan Coin, Tim Hubbard, Thomas A. Down, Mhairi Marshall, Rita Barfoot, Sheila Seal and Sandra Hanks. Their work appears in journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

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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