Margaret Barrow

1.8k total citations
18 papers, 738 citations indexed

About

Margaret Barrow is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Genetics. According to data from OpenAlex, Margaret Barrow has authored 18 papers receiving a total of 738 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 7 papers in Genetics and 3 papers in Genetics. Recurrent topics in Margaret Barrow's work include Prenatal Substance Exposure Effects (5 papers), Birth, Development, and Health (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Margaret Barrow is often cited by papers focused on Prenatal Substance Exposure Effects (5 papers), Birth, Development, and Health (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Margaret Barrow collaborates with scholars based in United Kingdom, Australia and United States. Margaret Barrow's co-authors include Dian Donnai, Andrew O.M. Wilkie, George Davey Smith, Kapil Sayal, Elizabeth S. Draper, Ron Gray, Sarah J. Lewis, Rosa Alati, Jean Golding and Veronica J. Buckle and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Margaret Barrow

17 papers receiving 714 citations

Peers

Margaret Barrow

GENET

PPCH

GENET

Philippe Loget France

Roelof J. Odink Netherlands

Christine M. Armour Canada

Rabah M. Shawky Egypt

Adam Brook United Kingdom

K. H. Gustavson Sweden

Susan Holloway United Kingdom

Lise Duranteau France

Christina Zaleski United States

Eric A. Wulfsberg United States

Philippe Loget France

Margaret Barrow

291 ×0.9

GENET

385 ×1.5

281 ×1.2

PPCH

23 ×0.3

GENET

53 ×0.7

Citations per year, relative to Margaret Barrow Margaret Barrow (= 1×) peers Philippe Loget

Countries citing papers authored by Margaret Barrow

Since Specialization

Citations

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

Fields of papers citing papers by Margaret Barrow

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Margaret Barrow

This figure shows the co-authorship network connecting the top 25 collaborators of Margaret Barrow. A scholar is included among the top collaborators of Margaret Barrow 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 Margaret Barrow. Margaret Barrow is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

Sayal, Kapil, Jon Heron, Elizabeth S. Draper, et al.. (2014). Prenatal exposure to binge pattern of alcohol consumption: mental health and learning outcomes at age 11. European Child & Adolescent Psychiatry. 23(10). 891–899. 36 indexed citations

Sayal, Kapil, Elizabeth S. Draper, Ryan Fraser, et al.. (2013). Light drinking in pregnancy and mid-childhood mental health and learning outcomes. Archives of Disease in Childhood. 98(2). 107–11. 22 indexed citations

Zuccolo, Luisa, Sarah J. Lewis, George Davey Smith, et al.. (2013). Prenatal alcohol exposure and offspring cognition and school performance. A ‘Mendelian randomization’ natural experiment. International Journal of Epidemiology. 42(5). 1358–1370. 57 indexed citations

Lewis, Sarah J., Luisa Zuccolo, George Davey Smith, et al.. (2012). Fetal Alcohol Exposure and IQ at Age 8: Evidence from a Population-Based Birth-Cohort Study. PLoS ONE. 7(11). e49407–e49407. 74 indexed citations

Ogi, Tomoo, Sarah Walker, Tom Stiff, et al.. (2012). Identification of the First ATRIP–Deficient Patient and Novel Mutations in ATR Define a Clinical Spectrum for ATR–ATRIP Seckel Syndrome. PLoS Genetics. 8(11). e1002945–e1002945. 79 indexed citations

Barrow, Margaret, et al.. (2011). Diagnosis of fetal alcohol syndrome: emphasis on early detection.. 85–107. 3 indexed citations

Özgen, Mihriban Heval, Emma van Daalen, PF Bolton, et al.. (2009). Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders. Clinical Genetics. 76(4). 348–356. 31 indexed citations

Navti, Osric, Esther Kinning, Pradeep Vasudevan, et al.. (2009). Review of perinatal management of arthrogryposis at a large UK teaching hospital serving a multiethnic population. Prenatal Diagnosis. 30(1). 49–56. 14 indexed citations

Kinning, Esther & Margaret Barrow. (2008). Arthrogryposis in association with Peters' anomaly. Clinical Dysmorphology. 17(3). 177–179.

10.

Asai-Coakwell, Mika, Andrew J. Mungall, Margaret Barrow, et al.. (2008). A novel mechanistic spectrum underlies glaucoma-associated chromosome 6p25 copy number variation. Human Molecular Genetics. 17(22). 3446–3458. 36 indexed citations

11.

Watson, Peter H., Sarah Ramsden, Margaret Barrow, et al.. (2001). Angelman syndrome phenotype associated with mutations in MECP2.. Journal of Medical Genetics. 1 indexed citations

12.

Johnson, David, Sharon W. Horsley, Dominique M. Moloney, et al.. (1998). A Comprehensive Screen for TWIST Mutations in Patients with Craniosynostosis Identifies a New Microdeletion Syndrome of Chromosome Band 7p21.1. The American Journal of Human Genetics. 63(5). 1282–1293. 143 indexed citations

13.

Barrow, Margaret, et al.. (1994). The attitudes of midwives to maternal serum screeningfor Down's syndrome. Public Health. 108(2). 131–136. 32 indexed citations

14.

Kääriäinen, Helena, Margaret Barrow, & Raoul C. M. Hennekam. (1993). Bone dysplasia, midface hypoplasia, and deafness: Three new patients and review of the literature. American Journal of Medical Genetics. 46(2). 223–227. 11 indexed citations

15.

Donnai, Dian & Margaret Barrow. (1993). Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: A newly recognized autosomal recessive disorder?. American Journal of Medical Genetics. 47(5). 679–682. 61 indexed citations

16.

Narayan, Harini, et al.. (1993). Familial congenital diaphragmatic hernia: Prenatal diagnosis, management, and outcome. Prenatal Diagnosis. 13(10). 893–901. 8 indexed citations

17.

Wilkie, Andrew O.M., Veronica J. Buckle, Peter C. Harris, et al.. (1990). Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.. PubMed. 46(6). 1112–26. 110 indexed citations

18.

Fitzsimmons, J S, et al.. (1982). Fronto‐metaphyseaI dysplasia. Further delineation of the clinical syndrome. Clinical Genetics. 22(4). 195–205. 20 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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