Helen Byers

1.6k citations

30 papers · 651 indexed · h-index 14

Genetics top 5%
- BRCA gene mutations in cancer 17
- Genomic variations and chromosomal abnormalities 7
- Genetic Associations and Epidemiology 4
Cancer Research
- Cancer Genomics and Diagnostics 7
Oncology
- Global Cancer Incidence and Screening 5
- Cancer Risks and Factors 4
Reproductive Medicine top 10%
- Ovarian function and disorders 4
Pathology and Forensic Medicine
Public Health, Environmental and Occupational Health
- Reproductive Biology and Fertility 3

Co-authors: William G. Newman D. Gareth Evans Anthony Howell Elaine F. Harkness Adam R. Brentnall Jack Cuzick Elke M. van Veen Susan Astley
Cited by: Genetics Cancer Research Oncology
Partner nations: United Kingdom United States Egypt

In The Last Decade

Helen Byers

30 papers receiving 643 citations

Peers

Countries citing papers authored by Helen Byers

Since Specialization

Citations

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

Fields of papers citing papers by Helen Byers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Helen Byers, 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 Helen Byers Line = papers co-authored together Helen Byers links everyone, so they are left out of the graph.

All Works

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

20 of 20 papers shown

#	Work
1	Validation of lung cancer polygenic risk scores in a high-risk case-control cohort Mikey B Lebrett,Miriam J. Smith,Emma J. Crosbie,John Bowes,Helen Byers,D. Gareth Evans,Philip Crosbie	2023	4
2	Breast cancer risk stratification in women of screening age: Incremental effects of adding mammographic density, polygenic risk, and a gene panel D. Gareth Evans,Elke M. van Veen,Elaine F. Harkness,Adam R. Brentnall,Susan Astley,Helen Byers,Emma R. Woodward,Sarah Sampson,Jake Southworth,Sacha J. Howell,Anthony Maxwell,William G. Newman,Jack Cuzick,Anthony Howell	2022	30
3	Differential involvement of germline pathogenic variants in breast cancer genes between DCIS and low-grade invasive cancers D. Gareth Evans,Siva Sithambaram,Elke M. van Veen,George J. Burghel,Hélene Schlecht,Elaine F. Harkness,Helen Byers,Jamie M. Ellingford,Ashu Gandhi,Sacha J. Howell,Anthony Howell,Claire Forde,Fiona Lalloo,William G. Newman,Miriam J. Smith,Emma R. Woodward	2022	2
4	Clinical utility of testing for PALB2 and CHEK2 c.1100delC in breast and ovarian cancer Emma R. Woodward,Elke M. van Veen,Claire Forde,Elaine F. Harkness,Helen Byers,Jamie M. Ellingford,George J. Burghel,Helene Schlech,Naomi L. Bowers,Andrew J. Wallace,Sacha J. Howell,Anthony Howell,Fiona Lalloo,William G. Newman,Miriam J. Smith,D. Gareth Evans	2021	9
5	Extended gene panel testing in lobular breast cancer Elke M. van Veen,D. Gareth Evans,Elaine F. Harkness,Helen Byers,Jamie M. Ellingford,Emma R. Woodward,Naomi L. Bowers,Andrew J. Wallace,Sacha J. Howell,Anthony Howell,Fiona Lalloo,William G. Newman,Miriam J. Smith	2021	3
6	Breast cancer pathology and stage are better predicted by risk stratification models that include mammographic density and common genetic variants D. Gareth Evans,Elaine F. Harkness,Adam R. Brentnall,Elke M. van Veen,Susan Astley,Helen Byers,Sarah Sampson,Jake Southworth,Paula Stavrinos,Sacha J. Howell,Anthony Maxwell,Anthony Howell,William G. Newman,Jack Cuzick	2019	49
7	A Dominantly Inherited 5′ UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian Cancer D. Gareth Evans,Elke M. van Veen,Helen Byers,Andrew J. Wallace,Jamie M. Ellingford,Glenda M. Beaman,Javier Santoyo‐López,Timothy J. Aitman,Diana Eccles,Fiona Lalloo,Miriam J. Smith,William G. Newman	2018	57
8	AMH type II receptor and AMH gene polymorphisms are not associated with ovarian reserve, response, or outcomes in ovarian stimulation Christian Cerra,William G. Newman,Dalia Tohlob,Helen Byers,Gregory Horne,Stephen A. Roberts,Lamiya Mohiyiddeen	2016	10
9	Sensitivity of BRCA1/2 testing in high-risk breast/ovarian/male breast cancer families: little contribution of comprehensive RNA/NGS panel testing Helen Byers,Yvonne Wallis,Elke M. van Veen,Fiona Lalloo,Kim Reay,Philip Smith,Andrew J. Wallace,Naomi L. Bowers,William G. Newman,D. Gareth Evans	2016	24
10	Relationship of ZNF423 and CTSO with breast cancer risk in two randomised tamoxifen prevention trials Adam R. Brentnall,Jack Cuzick,Helen Byers,Corrinne V. Segal,Caroline Reuter,Simone Detre,Ivana Šestak,Anthony Howell,Trevor J. Powles,William G. Newman,Mitch Dowsett	2016	6
11	Association of a promoter polymorphism in FSHR with ovarian reserve and response to ovarian stimulation in women undergoing assisted reproductive treatment Dalia Tohlob,Ekbal Abo Hashem,Nawal A. Ghareeb,Mohammed Ghanem,Reham M. El-Farahaty,Helen Byers,Philip A. Pemberton,Stephen A. Roberts,William G. Newman,Lamiya Mohiyiddeen	2016	13
12	A synonymous variant in TREX1 is associated with systemic sclerosis and severe digital ischaemia Michael Hughes,J. Little,Ariane L. Herrick,Sudeep Pushpakom,Helen Byers,Jane Worthington,William G. Newman	2016	4
13	Detection of a mosaic PIK3CA mutation in dental DNA from a child with megalencephaly capillary malformation syndrome John McDermott,Helen Byers,Jill Clayton‐Smith	2015	8
14	Intronic splicing mutations in PTCH1 cause Gorlin syndrome Zaynab Bholah,Miriam J. Smith,Helen Byers,Emma Miles,D. Gareth Evans,William G. Newman	2014	24
15	Identification of a novel familial FGF16 mutation in metacarpal 4–5 fusion Benedict Jones,Helen Byers,J S Watson,William G. Newman	2014	7
16	FSH receptor genotype does not predict metaphase-II oocyte output or fertilization rates in ICSI patients Lamiya Mohiyiddeen,William G. Newman,Christian Cerra,Gregory Horne,Betselot Mulugeta,Helen Byers,Stephen A. Roberts,Luciano G. Nardo	2013	5
17	Spontaneous ovarian hyperstimulation syndrome: case report, pathophysiological classification and diagnostic algorithm Nikoletta Panagiotopoulou,Helen Byers,William G. Newman,Kalsang Bhatia	2013	12
18	Increased Rate of Phenocopies in All Age Groups in BRCA1/BRCA2 Mutation Kindred, but Increased Prospective Breast Cancer Risk Is Confined to BRCA2 Mutation Carriers D. Gareth Evans,Sarah Ingham,Iain Buchan,Emma R. Woodward,Helen Byers,Anthony Howell,Eamonn R. Maher,William G. Newman,Fiona Lalloo	2013	11
19	G6PC3 mutations cause non-syndromic severe congenital neutropenia Siddharth Banka,Robert Wynn,Helen Byers,Peter D. Arkwright,William G. Newman	2012	12
20	Is multipleSNPtesting inBRCA2andBRCA1female carriers ready for use in clinical practice? Results from a large Genetic Centre in theUK S. Ingham,Jane Warwick,Helen Byers,Fiona Lalloo,William G. Newman,D. Gareth Evans	2012	10

About Helen Byers

Helen Byers is a scholar working on Genetics, Cancer Research and Reproductive Medicine, having authored 30 papers that have together received 651 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (17 papers), Genomic variations and chromosomal abnormalities (7 papers), Cancer Genomics and Diagnostics (7 papers), Global Cancer Incidence and Screening (5 papers), Genetic Associations and Epidemiology (4 papers), Cancer Risks and Factors (4 papers), Ovarian function and disorders (4 papers) and Reproductive Biology and Fertility (3 papers). The work is most often cited by research in Genetics (429 citations), Cancer Research (144 citations) and Oncology (217 citations). Helen Byers has collaborated with scholars based in United Kingdom, United States and Egypt. Frequent co-authors include William G. Newman, D. Gareth Evans, Anthony Howell, Elaine F. Harkness, Adam R. Brentnall, Jack Cuzick, Elke M. van Veen, Susan Astley, Sarah Sampson and Miriam J. Smith.

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