Jill Clayton‐Smith

28.0k citations
201 papers · 9.8k · 3 hit papers · h-index 51

Impact in

    • Pharmacological Effects and Toxicity Studies
    • Prenatal Screening and Diagnostics
  • Genetics top 0.1%
    • Genetic Syndromes and Imprinting
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities

Papers in

    • Genetic Syndromes and Imprinting 39
    • Genomic variations and chromosomal abnormalities 33
    • Genetics and Neurodevelopmental Disorders 20
    • Genomics and Rare Diseases 18
    • Epigenetics and DNA Methylation 22

Jill Clayton‐Smith

198 papers receiving 9.4k citations

Jill Clayton‐Smith's Hit Papers

Monotherapy treatment of epilepsy in pregnancy: congenital malformation outcomes in the child 2016 · 235 citations
2350+5+11Years since publication100200300400500

Peers

Jill Clayton‐Smith
Comparison fields: 5 of 142
  • Pediatrics, Perinatology and Child Health 3.6k
  • Genetics 5.0k
  • Psychiatry and Mental health 1.2k
  • Molecular Biology 3.2k
  • Public Health, Environmental and Occupational Health 1.2k
Replace Rosanna Weksberg with:
Rosanna Weksberg Canada
Merlin G. Butler United States
Eugen Boltshauser Switzerland
Eric Haan Australia
Judith L. Ross United States
Elaine H. Zackai United States
Ignatia B. Van den Veyver United States
Jean‐Pierre Fryns Belgium
Thomas Eggermann Germany
Claus Højbjerg Gravholt Denmark
Jill Clayton‐Smith relative to Rosanna Weksberg Canada Rosanna Weksberg's profile →
Citations per field
00.5×3.7×
Rosanna Weksberg · 1×
Citations per year

Countries citing papers authored by Jill Clayton‐Smith

Since Specialization
Citations

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

Fields of papers citing papers by Jill Clayton‐Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jill Clayton‐Smith. 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 Jill Clayton‐Smith. The network helps show where Jill Clayton‐Smith may publish in the future.

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 201 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Fetal antiepileptic drug exposure and cognitive outcomes at age 6 years (NEAD study): a prospective observational study
Hit paper breakdown →
2013520
2
Cognitive Function at 3 Years of Age after Fetal Exposure to Antiepileptic Drugs
Hit paper breakdown →
2009517
3 2006424
4 2003416
5 2009386
6 1995270
7 2013265
8 2003251
9 1991251
10
Monotherapy treatment of epilepsy in pregnancy: congenital malformation outcomes in the child
Hit paper breakdown →
2016235
11 2007216
12 2005187
13 2008180
14 1993173
15 2014166
16 1992136
17 2014131
18 2013126
19 2014125
20 2007119

About Jill Clayton‐Smith

Jill Clayton‐Smith is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Public Health, Environmental and Occupational Health, having authored 201 papers that have together received 9.8k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (39 papers), Genomic variations and chromosomal abnormalities (33 papers), Pharmacological Effects and Toxicity Studies (31 papers), Epigenetics and DNA Methylation (22 papers), Prenatal Screening and Diagnostics (20 papers), Genetics and Neurodevelopmental Disorders (20 papers), Genomics and Rare Diseases (18 papers) and Pregnancy and Medication Impact (14 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (3.6k citations), Genetics (5.0k citations), Psychiatry and Mental health (1.2k citations), Molecular Biology (3.2k citations) and Public Health, Environmental and Occupational Health (1.2k citations). Jill Clayton‐Smith has collaborated with scholars based in United Kingdom, United States and South Africa. Frequent co-authors include Gus A. Baker, Rebecca Bromley, Dian Donnai, Kimford J. Meador, David W. Loring, Morris J. Cohen, Laura A. Kalayjian, Page B. Pennell, Michael Privitera and Joyce Liporace. Their work appears in journals such as Journal of Medical Genetics, European Journal of Medical Genetics, European Journal of Human Genetics, Clinical Genetics and The American Journal of Human Genetics.

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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