Raheleh Rahbari

5.2k citations

27 papers · 1.1k indexed · h-index 12

Molecular Biology
Genetics top 5%
Cancer Research top 5%
Plant Science
Pediatrics, Perinatology and Child Health top 10%

Co-authors: Matthew E. Hurles Sarah Lindsay Michael R. Stratton Arthur Wüster Ludmil B. Alexandrov Saeed Al Turki David J. Porteous Andrew D. Morris
Topics: Cancer Genomics and Diagnostics (16 papers)Chromosomal and Genetic Variations (6 papers)CRISPR and Genetic Engineering (5 papers)
Cited by: Cancer Research Genetics Aging
Journals: Nature Nucleic Acids Research Nature Communications
Partner nations: United Kingdom United States France

In The Last Decade

Raheleh Rahbari

25 papers receiving 1.1k citations

Peers

Countries citing papers authored by Raheleh Rahbari

Since Specialization

Citations

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

Fields of papers citing papers by Raheleh Rahbari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raheleh Rahbari

This figure shows the co-authorship network connecting the top 25 collaborators of Raheleh Rahbari. A scholar is included among the top collaborators of Raheleh Rahbari 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 Raheleh Rahbari. Raheleh Rahbari 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 impact of ancestral, genetic, and environmental influences on germline de novo mutation rates and spectra 2025 ·Nature Communications ·(unknown),(unknown),Qin Qin Huang,Rashesh Sanghvi,Daniel Malawsky,Joanna Kaplanis,Matthew D. C. Neville,Felix R. Day,Raheleh Rahbari,Aylwyn Scally,Hilary C. Martin	0
2	Complex de novo structural variants are an underestimated cause of rare disorders 2025 ·Nature Communications ·Hyunchul Jung,Tsun-Po Yang,Susan Walker,Petr Danecek,(unknown),Matthew D. C. Neville,Joseph Christopher,Isidro Cortés‐Ciriano,Helen V. Firth,Aylwyn Scally,Matthew E. Hurles,Peter J. Campbell,Raheleh Rahbari	0
3	Investigating the origins of the mutational signatures in cancer 2025 ·Nucleic Acids Research ·Gunnar Boysen,Ludmil B. Alexandrov,Raheleh Rahbari,Intawat Nookaew,David W. Ussery,Mu‐Rong Chao,Chiung‐Wen Hu,Marcus S. Cooke	2
4	Hotspots of human mutation point to clonal expansions in spermatogonia 2025 ·Nature ·Vladimir B. Seplyarskiy,(unknown),Evan Koch,(unknown),Matthew D. C. Neville,Raheleh Rahbari,Shamil Sunyaev	2
5	De novo detection of somatic mutations in high-throughput single-cell profiling data sets 2023 ·Nature Biotechnology ·Francesc Muyas,Carolin M. Sauer,Jose Espejo Valle-Inclán,Ruoyan Li,Raheleh Rahbari,Thomas J. Mitchell,Sahand Hormoz,Isidro Cortés‐Ciriano	43
6	Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair 2023 ·Nature Communications ·Kitty Sherwood,(unknown),(unknown),Lynn Martin,Archie Campbell,Raheleh Rahbari,(unknown),Duncan Sproul,Andrew Green,Julian R. Sampson,Alan Donaldson,Kai‐Ren Ong,Karl Heinimann,Maartje Nielsen,Huw Thomas,Andrew Latchford,Claire Palles,Ian Tomlinson	7
7	A naturally occurring variant of MBD4 causes maternal germline hypermutation in primates 2023 ·Genome Research ·(unknown),Rashesh Sanghvi,Samuel M. Peterson,(unknown),(unknown),Raheleh Rahbari,Donald F. Conrad	7
8	Genetic and chemotherapeutic influences on germline hypermutation 2022 ·Nature ·Joanna Kaplanis,(unknown),Rashesh Sanghvi,Matthew D. C. Neville,Petr Danecek,Tim Coorens,Elena Prigmore,Patrick Short,Giuseppe Gallone,Jeremy F. McRae,Loukas Moutsianas,Chris A. Odhams,Jenny Carmichael,Angela Barnicoat,Helen V. Firth,Patrick O’Brien,Raheleh Rahbari,Matthew E. Hurles	49
9	Somatic Mutations Detected in Parkinson Disease Could Affect Genes With a Role in Synaptic and Neuronal Processes 2022 ·SHILAP Revista de lepidopterología ·Irene Lobón,Manuel Solís-Moruno,David Juan,Ashraf Muhaisen,Federico Abascal,Paula Esteller-Cucala,Raquel García-Pérez,M. J. Martí,Eduardo Tolosa,Jesús Ávila,Raheleh Rahbari,Tomàs Marquès‐Bonet,Ferrán Casals,Eduardo Soriano	9
10	Extensive phylogenies of human development inferred from somatic mutations 2021 ·Nature ·Tim Coorens,Luiza Moore,Philip S. Robinson,Rashesh Sanghvi,Joseph Christopher,James Hewinson,Moritz J. Przybilla,Andrew Lawson,Michael Spencer Chapman,Alex Cagan,Thomas R. W. Oliver,Matthew D. C. Neville,Yvette Hooks,Ayesha Noorani,Thomas J. Mitchell,Rebecca C. Fitzgerald,Peter J. Campbell,Iñigo Martincorena,Raheleh Rahbari,Michael R. Stratton	75
11	Increased somatic mutation burdens in normal human cells due to defective DNA polymerases 2021 ·Nature Genetics ·Philip S. Robinson,Tim Coorens,Claire Palles,Emily Mitchell,Federico Abascal,Sigurgeir Ólafsson,Bernard C. H. Lee,Andrew Lawson,Henry Lee-Six,Luiza Moore,Mathijs A. Sanders,James Hewinson,Lynn Martin,Claudia M.A. Pinna,Sara Galavotti,Raheleh Rahbari,Peter J. Campbell,Iñigo Martincorena,Ian Tomlinson,Michael R. Stratton	94
12	Increased somatic mutation burdens in normal human cells due to defective DNA polymerases 2021 ·EUR Research Repository (Erasmus University Rotterdam) ·Philip S. Robinson,Tim Coorens,Claire Palles,Emily Mitchell,Federico Abascal,Sigurgeir Ólafsson,Bernard C. H. Lee,Andrew Lawson,Henry Lee-Six,Luiza Moore,Mathijs A. Sanders,James Hewinson,Lynn Martin,Claudia M.A. Pinna,Sara Galavotti,Raheleh Rahbari,Peter J. Campbell,Iñigo Martincorena,Ian Tomlinson,Michael R. Stratton	1
13	Inherent Mosaicism and Extensive Mutation of Human Placentas 2021 ·Obstetrical & Gynecological Survey ·Tim Coorens,Thomas R. W. Oliver,Rashesh Sanghvi,Ulla Sovio,Emma Cook,Roser Vento‐Tormo,Muzlifah Haniffa,Matthew D. Young,Raheleh Rahbari,Neil J. Sebire,Peter J. Campbell,D. Stephen Charnock‐Jones,Gordon C. S. Smith,Sam Behjati	1
14	Inherent mosaicism and extensive mutation of human placentas 2021 ·Nature ·Tim Coorens,Thomas R. W. Oliver,Rashesh Sanghvi,Ulla Sovio,Emma Cook,Roser Vento‐Tormo,Muzlifah Haniffa,Matthew D. Young,Raheleh Rahbari,Neil J. Sebire,Peter J. Campbell,D. Stephen Charnock‐Jones,Gordon C. S. Smith,Sam Behjati	120
15	Similarities and differences in patterns of germline mutation between mice and humans 2019 ·Nature Communications ·Sarah Lindsay,Raheleh Rahbari,Joanna Kaplanis,Thomas Keane,Matthew E. Hurles	78
16	Detection of structural mosaicism from targeted and whole-genome sequencing data 2017 ·Genome Research ·Daniel A. King,Alejandro Sifrim,Tomas Fitzgerald,Raheleh Rahbari,Emma Hobson,Tessa Homfray,Sahar Mansour,Sarju Mehta,(unknown),Susan Tomkins,Pradeep Vasudevan,Matthew E. Hurles,(unknown)	38
17	Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processes 2017 ·Nature Communications ·Vagheesh M. Narasimhan,Raheleh Rahbari,Aylwyn Scally,Arthur Wüster,Dan Mason,Yali Xue,John Wright,Richard C. Trembath,Eamonn R. Maher,David A. van Heel,Adam Auton,Matthew E. Hurles,Chris Tyler‐Smith,Richard Durbin	54
18	Timing, rates and spectra of human germline mutation 2015 ·Nature Genetics ·Raheleh Rahbari,Arthur Wüster,Sarah Lindsay,Robert J. Hardwick,Ludmil B. Alexandrov,Saeed Al Turki,Anna F. Dominiczak,Andrew D. Morris,David J. Porteous,Blair H. Smith,Michael R. Stratton,Matthew E. Hurles	381
19	Transduction-Specific ATLAS Reveals a Cohort of Highly Active L1 Retrotransposons in Human Populations 2013 ·Human Mutation ·Catriona Macfarlane,(unknown),Raheleh Rahbari,Christine R. Beck,(unknown),(unknown),John V. Moran,Richard M. Badge	31
20	IAP Display: A Simple Method to Identify Mouse Strain Specific IAP Insertions 2010 ·Molecular Biotechnology ·(unknown),Raheleh Rahbari,Richard M. Badge	4

About Raheleh Rahbari

Raheleh Rahbari is a scholar working on Cancer Research, Genetics and Molecular Biology, having authored 27 papers that have together received 1.1k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (16 papers), Chromosomal and Genetic Variations (6 papers) and CRISPR and Genetic Engineering (5 papers). The work is most often cited by research in Cancer Research (342 citations), Genetics (504 citations) and Aging (21 citations). Raheleh Rahbari has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Matthew E. Hurles, Sarah Lindsay, Michael R. Stratton, Arthur Wüster, Ludmil B. Alexandrov, Saeed Al Turki, David J. Porteous, Andrew D. Morris, Anna F. Dominiczak and Robert J. Hardwick. Their work appears in journals such as Nature, Nucleic Acids Research and Nature Communications.

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