M Pembrey

776 total citations
21 papers, 518 citations indexed

About

M Pembrey is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, M Pembrey has authored 21 papers receiving a total of 518 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 4 papers in Pediatrics, Perinatology and Child Health and 2 papers in Molecular Biology. Recurrent topics in M Pembrey's work include Craniofacial Disorders and Treatments (3 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers) and Congenital limb and hand anomalies (2 papers). M Pembrey is often cited by papers focused on Craniofacial Disorders and Treatments (3 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers) and Congenital limb and hand anomalies (2 papers). M Pembrey collaborates with scholars based in United Kingdom, India and Australia. M Pembrey's co-authors include Rebecca Coffey, Jane Somerville, Ori Scott, Paul Brennan, Julian Little, L. D. Allan, B Keeton, E D Silove, S Holloway and John Deanfield and has published in prestigious journals such as The Lancet, Journal of Thrombosis and Haemostasis and Journal of Medical Genetics.

In The Last Decade

M Pembrey

20 papers receiving 479 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
M Pembrey United Kingdom	9	208	205	145	130	116	21	518
P. Martul Spain	15	138 0.7×	96 0.5×	136 0.9×	88 0.7×	12 0.1×	31	575
Bülent Hacıhamdioğlu Türkiye	15	181 0.9×	91 0.4×	148 1.0×	80 0.6×	57 0.5×	54	564
C. P. Schwarze Germany	15	234 1.1×	35 0.2×	249 1.7×	89 0.7×	111 1.0×	26	671
Juliane Léger France	15	320 1.5×	61 0.3×	357 2.5×	108 0.8×	35 0.3×	26	1.1k
Nurgün Kandemir Türkiye	15	182 0.9×	32 0.2×	137 0.9×	139 1.1×	39 0.3×	46	710
J. M. Wit Netherlands	7	179 0.9×	69 0.3×	272 1.9×	101 0.8×	32 0.3×	13	533
Shunsuke Minami Japan	11	80 0.4×	111 0.5×	58 0.4×	189 1.5×	30 0.3×	15	679
Şükran Poyrazoğlu Türkiye	18	287 1.4×	46 0.2×	244 1.7×	133 1.0×	28 0.2×	84	794
Ergün Çetinkaya Türkiye	13	125 0.6×	41 0.2×	108 0.7×	57 0.4×	21 0.2×	30	476
Giuseppa Patti Italy	16	206 1.0×	47 0.2×	149 1.0×	97 0.7×	34 0.3×	51	609

Countries citing papers authored by M Pembrey

Since Specialization

Citations

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

Fields of papers citing papers by M Pembrey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M Pembrey

This figure shows the co-authorship network connecting the top 25 collaborators of M Pembrey. A scholar is included among the top collaborators of M 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 M Pembrey. M 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

Dudding, Tracy, Jon Heron, Eha Nurk, et al.. (2008). Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysis. Journal of Thrombosis and Haemostasis. 6(11). 1868–1875. 42 indexed citations

Pembrey, M. (2004). The Avon Longitudinal Study of Parents and Children (ALSPAC): a resource for genetic epidemiology. European Journal of Endocrinology. 151(Suppl_3). U125–U129. 29 indexed citations

Pembrey, M, et al.. (2000). The Gly972Arg variant in insulin receptor substrate-1 is not associated with birthweight in contemporary English children. UCL Discovery (University College London). 2 indexed citations

Burn, John, Paul Brennan, Julian Little, et al.. (1998). Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study. The Lancet. 351(9099). 311–316. 251 indexed citations

Cohen, Mazal, Mary C. Francis, Rebecca Coffey, M Pembrey, & L. M. Luxon. (1997). Abnormal Audiograms and Elevated Acoustic Reflex Thresholds in Obligate Carriers of Autosomal Recessive Non-Syndromic Hearing Loss. Acta Oto-Laryngologica. 117(3). 337–342. 1 indexed citations

Cohen, Mazal, Mary C. Francis, L. M. Luxon, et al.. (1996). Dips on Békésy or Audioscan Fail to Identify Carriers of Autosomal Recessive Non-Syndromic Hearing Loss. Acta Oto-Laryngologica. 116(4). 521–527. 6 indexed citations

Baraitser, M, et al.. (1993). Okihiro syndrome: thenar hypoplasia and Duane anomaly in three generations.. PubMed. 2(3). 237–40. 8 indexed citations

Clayton‐Smith, Jill, T. Webb, S. Robb, et al.. (1992). Further evidence for dominant inheritance at the chromosome 15q11‐13 locus in familial angelman syndrome. American Journal of Medical Genetics. 44(2). 256–260. 29 indexed citations

Cohen, Brian, I. Karen Temple, C. Michael Hall, et al.. (1991). Microtia and short stature: a new syndrome.. Journal of Medical Genetics. 28(11). 786–790. 13 indexed citations

10.

Temple, I. Karen, et al.. (1989). Dominantly inherited cleft lip and palate in two families.. Journal of Medical Genetics. 26(6). 386–389. 27 indexed citations

11.

Ponder, Bruce A.J., Nick Finer, Rebecca Coffey, et al.. (1988). Family Screening in Medullary Thyroid Carcinoma Presenting Without a Family History. QJM. 67(252). 299–308. 27 indexed citations

12.

Thompson, Elizabeth M., Sarah Hill, James V. Leonard, & M Pembrey. (1987). A girl with the Weaver syndrome.. Journal of Medical Genetics. 24(4). 232–234. 8 indexed citations

13.

Pembrey, M. (1983). Clinical application of recombinant DNA techniques in families with genetic disease.. PubMed. 29(6). 546, 548–51. 1 indexed citations

14.

Pembrey, M. (1979). Blood Groups and Diseases. A Study of Associations of Diseases with Blood Groups and Other Polymorphisms. Oxford Monographs on Medical Genetics. Journal of Medical Genetics. 16(3). 241–242. 1 indexed citations

15.

Pembrey, M. (1972). Discordant identical twins. VI. Psoriasis and migraine.. PubMed. 209(254). 846–50. 4 indexed citations

16.

Pembrey, M. (1972). Discordant identical twins. V. Neural tube defects.. PubMed. 209(253). 709–12. 3 indexed citations

17.

Pembrey, M. (1972). Discordant identical twins. I. Bronchial asthma.. PubMed. 209(249). 110–3. 1 indexed citations

18.

Pembrey, M. (1972). Discordant identical twins. II. Parkinsonism.. PubMed. 209(250). 240–3. 4 indexed citations

19.

Pembrey, M. (1971). Problems of Man's Biology. BMJ. 3(5766). 123.2–123. 7 indexed citations

20.

Weatherall, D. J., et al.. (1970). FAMILIAL SIDEROBLASTIC ANÆMIA: PROBLEM OF Xg AND X CHROMOSOME INACTIVATION. The Lancet. 296(7676). 744–748. 41 indexed citations

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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