Gemma Buck

11.6k citations

36 papers · 9.4k · 5 hit papers · h-index 26

Impact in

Cancer Research top 0.5%
- Cancer Genomics and Diagnostics
Genetics top 1%
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Glioma Diagnosis and Treatment
- Genomic variations and chromosomal abnormalities

Papers in

Genetics 16
- Genetics and Neurodevelopmental Disorders 7
- Genetic Associations and Epidemiology 6
- Genomic variations and chromosomal abnormalities 3
- Myeloproliferative Neoplasms: Diagnosis and Treatment 2
Cancer Research 6
- Cancer Genomics and Diagnostics 6

Co-authors: Supat Thongjuea (2 shared papers)Alba Rodríguez-Meira (3 shared papers)Bethan Psaila (3 shared papers)Adam J. Mead (3 shared papers)Benjamin J. Povinelli (1 shared paper)Nikolaos Sousos (2 shared papers)Nikolaos Barkas (1 shared paper)Angela D. Hamblin (2 shared papers)
Journals: Nature Genetics (6 papers)Nature (4 papers)The American Journal of Human Genetics (4 papers)Cancer Research (3 papers)Blood (2 papers)
Partner nations: United Kingdom United States Australia

In The Last Decade

Gemma Buck

35 papers receiving 9.2k citations

Gemma Buck's Hit Papers

5 papers align trajectories log scale

The genetic architecture of type 2 diabetes 2016 · 845 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2016 Nature
2010 Nature
2009 Nature Genetics
2009 Nature Genetics
2007 Nature

Peers

Countries citing papers authored by Gemma Buck

Since Specialization

Citations

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

Fields of papers citing papers by Gemma Buck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Gemma Buck, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Gemma Buck Line = papers co-authored together Gemma Buck links everyone, so they are left out of the graph.

All Works

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

20 of 20 papers shown

Showing the 20 most-cited of 36 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Patterns of somatic mutation in human cancer genomes Nature ·Christopher D. Greenman, Philip Stephens, Raffaella Smith, Gillian L. Dalgliesh, Chris Hunter, Graham R. Bignell, Helen Ruth Davies, Jon W. Teague Hit paper breakdown →	2007	2481
2	Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes Nature ·Gillian L. Dalgliesh, Kyle Furge, Chris Greenman, Lina Chen, Graham R. Bignell, Adam P. Butler, Helen Ruth Davies, Sarah Edkins Hit paper breakdown →	2010	990
3	The genetic architecture of type 2 diabetes Nature ·Christian Fuchsberger, Jason A. Flannick, Tanya M. Teslovich, Anubha Mahajan, Vineeta Agarwala, Kyle J. Gaulton, Clement Ma, Pierre Fontanillas Hit paper breakdown →	2016	845
4	Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer Nature Genetics ·Gijs W van Haaften, Gillian L. Dalgliesh, Helen Ruth Davies, Lina Chen, Graham R. Bignell, Chris Greenman, Sarah Edkins, Claire W. Hardy Hit paper breakdown →	2009	646
5	Signatures of mutation and selection in the cancer genome Nature ·Graham R. Bignell, Chris Greenman, Helen Ruth Davies, Adam P. Butler, Sarah Edkins, Gemma Buck, Lina Chen, David M. Beare	2010	578
6	A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation Nature Genetics ·Patrick S. Tarpey, Raffaella Smith, Erin Pleasance, Annabel C. Whibley, Sarah Edkins, Claire W. Hardy, Sarah O’Meara, Calli Latimer Hit paper breakdown →	2009	505
7	Somatic Mutations of the Protein Kinase Gene Family in Human Lung Cancer Cancer Research ·Helen Ruth Davies, Chris Hunter, Raffaella Smith, Philip Stephens, Chris Greenman, Graham R. Bignell, Jon W. Teague, Adam P. Butler	2005	380
8	A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy Cancer Research ·Chris Hunter, Raffaella Smith, Daniel P. Cahill, Philip Stephens, Jon W. Teague, Chris Greenman, Sarah Edkins, Graham R. Bignell	2006	375
9	Mutation analysis of 24 known cancer genes in the NCI-60 cell line set Molecular Cancer Therapeutics ·Ogechi N. Ikediobi, Helen Ruth Davies, Graham R. Bignell, Sarah Edkins, Sarah O’Meara, Thomas Santarius, Tim Avis, Syd Barthorpe	2006	362
10	X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment Nature Genetics ·Leanne M. Dibbens, Patrick S. Tarpey, Kim Hynes, Marta A. Bayly, Ingrid Eileen Scheffer, Raffaella Smith, Jamee M. Bomar, Edwina Sutton	2008	354
11	A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer Nature Genetics ·Philip Stephens, Sarah Edkins, Helen Ruth Davies, Chris Greenman, Chris Hunter, Graham R. Bignell, Jon W. Teague, Raffaella Smith	2005	274
12	Unravelling Intratumoral Heterogeneity through High-Sensitivity Single-Cell Mutational Analysis and Parallel RNA Sequencing Molecular Cell ·Alba Rodríguez-Meira, Gemma Buck, Sally‐Ann Clark, Benjamin J. Povinelli, Verónica Alcolea, Eleni Louka, Simon J. McGowan, Angela D. Hamblin	2019	248
13	Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation Nature Genetics ·Patrick S. Tarpey, Frances Lucy Raymond, Lam Son Nguyen, Jayson D. Rodriguez, Anna Hackett, Lucianne Vandeleur, Raffaella Smith, Cheryl Shoubridge	2007	230
14	Mutations in CUL4B, Which Encodes a Ubiquitin E3 Ligase Subunit, Cause an X-linked Mental Retardation Syndrome Associated with Aggressive Outbursts, Seizures, Relative Macrocephaly, Central Obesity, Hypogonadism, Pes Cavus, and Tremor The American Journal of Human Genetics ·Patrick S. Tarpey, Frances Lucy Raymond, Sarah O’Meara, Sarah Edkins, Jon W. Teague, Adam P. Butler, Ed Dicks, Calli Tofts	2007	197
15	Mutations in ZDHHC9, Which Encodes a Palmitoyltransferase of NRAS and HRAS, Cause X-Linked Mental Retardation Associated with a Marfanoid Habitus The American Journal of Human Genetics ·Frances Lucy Raymond, Patrick S. Tarpey, Sarah Edkins, Calli Tofts, Sarah O’Meara, Jon W. Teague, Adam P. Butler, Syd Barthorpe	2007	143
16	Mutations in the Gene Encoding the Sigma 2 Subunit of the Adaptor Protein 1 Complex, AP1S2, Cause X-Linked Mental Retardation The American Journal of Human Genetics ·Patrick S. Tarpey, Jon W. Teague, Sarah Edkins, Sarah O’Meara, Tim Avis, Syd Barthorpe, Gemma Buck, Adam P. Butler	2006	98
17	Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus PLoS Genetics ·Anubha Mahajan, Xueling Sim, Hui Jin Ng, Alisa Knodle Manning, Manuel A. Rivas, Heather M. Highland, Adam E. Locke, Niels Grarup	2015	93
18	Sequence analysis of the protein kinase gene family in human testicular germ‐cell tumors of adolescents and adults Genes Chromosomes and Cancer ·Graham R. Bignell, Raffaella Smith, Chris Hunter, Philip Stephens, Helen Ruth Davies, Chris Greenman, Jon W. Teague, Adam P. Butler	2005	82
19	Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk Nature Genetics ·Nick Orr, Alina Lemnrau, Rosie Cooke, Olivia Fletcher, Katarzyna Tomczyk, Michael Emlyn Jones, Nichola Johnson, Christopher J. Lord	2012	82
20	Genome-Wide Copy Number Variation Analysis in Extended Families and Unrelated Individuals Characterized for Musical Aptitude and Creativity in Music PLoS ONE ·Liisa Ukkola‐Vuoti, Chakravarthi Kanduri, Jaana Oikkonen, Gemma Buck, Christine Blancher, Pirre Raijas, Kai Karma, Harri J Lähdesmäki	2013	79

About Gemma Buck

Gemma Buck is a scholar working on Genetics, Cancer Research, Hematology, Genetics and Public Health, Environmental and Occupational Health, having authored 36 papers that have together received 9.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), Genetic Associations and Epidemiology (6 papers), Cancer Genomics and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (3 papers), Acute Lymphoblastic Leukemia research (2 papers), Pancreatic function and diabetes (2 papers), Single-cell and spatial transcriptomics (2 papers) and Myeloproliferative Neoplasms: Diagnosis and Treatment (2 papers). The work is most often cited by research in Cancer Research (1.7k citations), Genetics (2k citations), Molecular Biology (3.3k citations), Genetics (438 citations) and Oncology (712 citations). Gemma Buck has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Supat Thongjuea, Alba Rodríguez-Meira, Bethan Psaila, Adam J. Mead, Benjamin J. Povinelli, Nikolaos Sousos, Nikolaos Barkas, Angela D. Hamblin, Verónica Alcolea and Eleni Louka. Their work appears in journals such as Nature Genetics, Nature, The American Journal of Human Genetics, Cancer Research and Blood.

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

Gemma Buck

Impact in

Papers in i

In The Last Decade

Gemma Buck

Gemma Buck's Hit Papers

Peers

Countries citing papers authored by Gemma Buck

Fields of papers citing papers by Gemma Buck

All Works

About Gemma Buck

Explore authors with similar magnitude of impact

Papers in