Marcus Pembrey

18.4k total citations · 1 hit paper
161 papers, 10.2k citations indexed

About

Marcus Pembrey is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Marcus Pembrey has authored 161 papers receiving a total of 10.2k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Molecular Biology, 60 papers in Genetics and 46 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Marcus Pembrey's work include Birth, Development, and Health (29 papers), Epigenetics and DNA Methylation (28 papers) and Genetics and Neurodevelopmental Disorders (25 papers). Marcus Pembrey is often cited by papers focused on Birth, Development, and Health (29 papers), Epigenetics and DNA Methylation (28 papers) and Genetics and Neurodevelopmental Disorders (25 papers). Marcus Pembrey collaborates with scholars based in United Kingdom, India and United States. Marcus Pembrey's co-authors include Lars Olov Bygren, Jean Golding, Gunnar Kaati, Michael Sjöstróm, Kate Northstone, D. J. Weatherall, William Reardon, Anthony P. Monaco, Sören Edvinsson and Jill Clayton‐Smith and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Marcus Pembrey

158 papers receiving 9.7k citations

Hit 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.

Sex-specific, male-line transgenerational responses in humans

2005 768 citations Marcus Pembrey, Lars Olov Bygren et al. profile →

Peers

Countries citing papers authored by Marcus Pembrey

Since Specialization

Citations

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

Fields of papers citing papers by Marcus Pembrey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marcus Pembrey

This figure shows the co-authorship network connecting the top 25 collaborators of Marcus Pembrey. A scholar is included among the top collaborators of Marcus Pembrey 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 Marcus Pembrey. Marcus Pembrey 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	Grandmothers’ smoking in pregnancy is associated with a reduced prevalence of early-onset myopia 2019 ·Scientific Reports ·Cathy Williams, Matthew Suderman, Jeremy A. Guggenheim, Genette Ellis, Steven Gregory, Yasmin Iles‐Caven, Kate Northstone, Jean Golding, Marcus Pembrey	19
2	Grand-maternal smoking in pregnancy and grandchild’s autistic traits and diagnosed autism 2017 ·Scientific Reports ·Jean Golding, Genette Ellis, Steven Gregory, Karen Birmingham, Yasmin Iles‐Caven, Dheeraj Rai, Marcus Pembrey	55
3	Human transgenerational responses to early-life experience: potential impact on development, health and biomedical research 2014 ·Journal of Medical Genetics ·Marcus Pembrey, Richard Saffery, Lars Olov Bygren, (unknown)	196
4	Prevalence and audiological features in carriers of GJB2 mutations, c.35delG and c.101T>C (p.M34T), in a UK population study 2012 ·BMJ Open ·Amanda Hall, Marcus Pembrey, Mark E. Lutman, Colin Steer, Maria Bitner‐Glindzicz	18
5	Inheritance of a copy number variant in the imprinted PHLDA2 gene promoter significantly increases fetal birth weight 2011 ·UCL Discovery (University College London) ·Miho Ishida, David Monk, (unknown), Sayeda Abu‐Amero, Jer Pin Chong, (unknown), Marcus Pembrey, (unknown), J. R. Whittaker, Philip Stanier, (unknown)	1
6	Association of the KIAA0319 Dyslexia Susceptibility Gene With Reading Skills in the General Population 2008 ·American Journal of Psychiatry ·Silvia Paracchini, Colin Steer, (unknown), Andrew P. Morris, Susan M. Ring, Thomas Scerri, John Stein, Marcus Pembrey, Jiannis Ragoussis, Jean Golding, Anthony P. Monaco	102
7	Human inheritance, differences and diseases: putting genes in their place. Part II 2008 ·Paediatric and Perinatal Epidemiology ·Marcus Pembrey	0
8	The search for genenotype/phenotype associations and the phenome scan 2005 ·Paediatric and Perinatal Epidemiology ·Richard W. Jones, Marcus Pembrey, Jean Golding, David Herrick	33
9	Investigation of UBE3A and MECP2 in Angelman syndrome (AS) and patients with features of AS 2003 ·American Journal of Medical Genetics Part A ·Megan P. Hitchins, Sarah Rickard, Fatima Dhalla, Bert B.A. de Vries, Robin Winter, Marcus Pembrey, Sue Malcolm	39
10	Social sex selection by preimplantation genetic diagnosis 2002 ·Reproductive BioMedicine Online ·Marcus Pembrey	12
11	Radiological malformations of the ear in pendred syndrome 1998 ·Clinical Radiology ·Peter Phelps, Rebecca A. Coffey, Richard C. Trembath, Linda Luxon, Ashley Grossman, K. E. Britton, P. Kendall‐Taylor, John M. Graham, (unknown), (unknown), Marcus Pembrey, William Reardon	184
12	Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome 1996 ·Clinical Endocrinology ·(unknown), John A.L. Armour, Beth Coyle, Rebecca Coffey, Ze’ev Hochberg, Marcus Pembrey, K. E. Britton, Ashley Grossman, William Reardon, Richard C. Trembath	13
13	Angelman syndrome associated with a maternal 15q11–13 deletion of less than 200 kb 1994 ·Human Molecular Genetics ·Jessica L. Buxton, (unknown), (unknown), Jill Clayton‐Smith, John Burn, Marcus Pembrey, S Malcolm	17
14	Neuro-otological Function in X-linked Hearing Loss: A Multipedigree Assessment and Correlation with Other Clinical Parameters 1993 ·Acta Oto-Laryngologica ·William Reardon, Susan Bellman, Peter Phelps, Marcus Pembrey, Linda Luxon	5
15	Angelman syndrome can result from uniparental paternal isodisomy 1990 ·Leicester Research Archive (University of Leicester) ·M.A. Ferguson‐Smith, (unknown), Jill Clayton‐Smith, (unknown), John A.L. Armour, (unknown), Marcus Pembrey	6
16	Close linkage of random DNA fragments from Xq 21.3–22 to X-linked agammaglobulinaemia (XLA) 1987 ·Human Genetics ·S Malcolm, Geneviève de Saint Basile, Benoı̂t Arveiler, YL Lau, Piroska E. Szabó, Alain Fischer, C Griscelli, Marianne Debré, Jean‐Louis Mandel, Robin E. Callard, M. E. Robertson, Judith A. Goodship, Marcus Pembrey, R J Levinsky	50
17	First trimester prenatal diagnosis and detection of carriers of haemophilia A using the linked DNA probe DX13. 1985 ·BMJ ·R M Winter, Katherine L. Harper, E. Goldman, R.S. Mibashan, (unknown), Charles H. Rodeck, R. Penketh, R. H. T. Ward, R. M. Hardisty, Marcus Pembrey	24
18	In Memoriam: Professor C. O. Carter, MA, DM Oxon, FRCP 1984 ·American Journal of Medical Genetics ·Marcus Pembrey	3
19	Abstracts of the meeting of the Clinical Genetics Society held on 7 and 8 April 1983 at the University of Cambridge 1983 ·Journal of Medical Genetics ·Peter S. Harper, Marcus Pembrey, E. Rhys Davies, Genette Ellis, R. Williamson, (unknown), C.‐D. Walker, Robin Winter	2
20	Thalassaemia in the British 1973 ·BMJ ·Huxley Knox-Macaulay, D. J. Weatherall, J. B. Clegg, Marcus Pembrey	54

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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