L. Leigh Field

4.7k total citations
43 papers, 2.2k citations indexed

About

L. Leigh Field is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, L. Leigh Field has authored 43 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 19 papers in Molecular Biology and 8 papers in Surgery. Recurrent topics in L. Leigh Field's work include Cleft Lip and Palate Research (12 papers), Craniofacial Disorders and Treatments (10 papers) and Diabetes and associated disorders (4 papers). L. Leigh Field is often cited by papers focused on Cleft Lip and Palate Research (12 papers), Craniofacial Disorders and Treatments (10 papers) and Diabetes and associated disorders (4 papers). L. Leigh Field collaborates with scholars based in Canada, United States and Denmark. L. Leigh Field's co-authors include Rose Tobias, Mary L. Marazita, Bonnie J. Kaplan, Robert S. Sparkes, Steve J. Funderburk, Maryellen C. Sparkes, Margaret E. Cooper, William F. Benedict, A. Linn Murphree and Robert W. Lingua and has published in prestigious journals such as Science, Nature Genetics and Diabetes.

In The Last Decade

L. Leigh Field

43 papers receiving 2.1k citations

Peers

L. Leigh Field
Bruce Bennetts Australia
S Gilgenkrantz France
Helen Stewart United Kingdom
Shivanand R. Patil United States
Vazken M. Der Kaloustian Canada
Mohnish Suri United Kingdom
Jennifer A. Donald Australia
Dvorah Abeliovich Israel
Ruth Newbury‐Ecob United Kingdom
Stefan J. White Netherlands
Bruce Bennetts Australia
L. Leigh Field
Citations per year, relative to L. Leigh Field L. Leigh Field (= 1×) peers Bruce Bennetts

Countries citing papers authored by L. Leigh Field

Since Specialization
Citations

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

Fields of papers citing papers by L. Leigh Field

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by L. Leigh Field. 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 L. Leigh Field. The network helps show where L. Leigh Field may publish in the future.

Co-authorship network of co-authors of L. Leigh Field

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

All Works

20 of 20 papers shown
1.
Leslie, Elizabeth J., Jenna C. Carlson, John R. Shaffer, et al.. (2017). Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate. Human Genetics. 136(3). 275–286. 101 indexed citations
2.
Tran, Christopher, France Gagnon, K. Wigg, et al.. (2013). A family‐based association analysis and meta‐analysis of the reading disabilities candidate gene DYX1C1. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(2). 146–156. 16 indexed citations
3.
Dan, Meixia, et al.. (2012). Induction and activation of antiviral enzyme 2′,5′-oligoadenylate synthetase by in vitro transcribed insulin mRNA and other cellular RNAs. Molecular Biology Reports. 39(7). 7813–7822. 16 indexed citations
4.
5.
Shi, Min, Sandra Daack‐Hirsch, Kaare Christensen, et al.. (2007). X‐chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate. American Journal of Medical Genetics Part A. 143A(24). 3267–3272. 20 indexed citations
6.
Bonnevie‐Nielsen, V., L. Leigh Field, Min Li, et al.. (2005). Variation in Antiviral 2′,5′-Oligoadenylate Synthetase (2′5′AS) Enzyme Activity Is Controlled by a Single-Nucleotide Polymorphism at a Splice-Acceptor Site in the OAS1 Gene. The American Journal of Human Genetics. 76(4). 623–633. 117 indexed citations
7.
Field, L. Leigh, et al.. (2004). Genome scan for loci involved in nonsyndromic cleft lip with or without cleft palate in families from West Bengal, India. American Journal of Medical Genetics Part A. 130A(3). 265–271. 31 indexed citations
8.
Stephenson, Mary D., Maria S. Peñaherrera, Ruiwei Jiang, et al.. (2003). Skewed X-Chromosome Inactivation Is Associated with Trisomy in Women Ascertained on the Basis of Recurrent Spontaneous Abortion or Chromosomally Abnormal Pregnancies. The American Journal of Human Genetics. 72(2). 399–407. 64 indexed citations
9.
Marazita, Mary L., et al.. (2002). Genome Scan for Loci Involved in Cleft Lip With or Without Cleft Palate, in Chinese Multiplex Families. The American Journal of Human Genetics. 71(2). 349–364. 86 indexed citations
10.
Shi, Qinghua, Elizabeth Spriggs, L. Leigh Field, et al.. (2002). Absence of Age Effect on Meiotic Recombination between Human X and Y Chromosomes. The American Journal of Human Genetics. 71(2). 254–261. 34 indexed citations
11.
Shi, Qinghua, Elizabeth Spriggs, L. Leigh Field, et al.. (2001). Single sperm typing demonstrates that reduced recombination is associated with the production of aneuploid 24,XY human sperm. American Journal of Medical Genetics. 99(1). 34–38. 80 indexed citations
12.
Bech‐Hansen, N. Torben, et al.. (1998). Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23. Human Genetics. 103(2). 124–130. 30 indexed citations
13.
Woodside, D. Blake, L. Leigh Field, Paul E. Garfinkel, & Margus Heinmaa. (1998). Specificity of eating disorders diagnoses in families of probands with anorexia nervosa and bulimia nervosa. Comprehensive Psychiatry. 39(5). 261–264. 12 indexed citations
14.
Field, L. Leigh & Bonnie J. Kaplan. (1998). Absence of Linkage of Phonological Coding Dyslexia to Chromosome 6p23-p21.3 in a Large Family Data Set. The American Journal of Human Genetics. 63(5). 1448–1456. 76 indexed citations
15.
Barcellos, Lisa F., William Klitz, L. Leigh Field, et al.. (1997). Association Mapping of Disease Loci, by Use of a Pooled DNA Genomic Screen. The American Journal of Human Genetics. 61(3). 734–747. 190 indexed citations
16.
Field, L. Leigh, et al.. (1988). Immunoglobulin (GM and KM) allotypes in the Sikh population of India. American Journal of Physical Anthropology. 75(1). 31–35. 3 indexed citations
17.
Haile, Robert W., Alisa M. Goldstein, L. Leigh Field, Mary L. Marazita, & D. C. Rao. (1985). A linkage analysis of the Gm locus and multiple sclerosis. Genetic Epidemiology. 2(1). 29–34. 10 indexed citations
18.
Petersen, Gloria M., Jerome I. Rotter, L. Leigh Field, et al.. (1983). The Tay-Sachs disease gene in North American Jewish populations: geographic variations and origin.. PubMed. 35(6). 1258–69. 67 indexed citations
19.
Field, L. Leigh, J. R. Heckenlively, R.S. Sparkes, et al.. (1982). Linkage analysis of five pedigrees affected with typical autosomal dominant retinitis pigmentosa.. Journal of Medical Genetics. 19(4). 266–270. 25 indexed citations
20.
Field, L. Leigh, J. R. Heckenlively, R.S. Sparkes, et al.. (1980). Linkage analysis of several families with dominant form retinitis pigmentosa. The American Journal of Human Genetics. 32(6). 105. 1 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Bruce Bennetts Breakdown of academic impact, for papers by S Gilgenkrantz Breakdown of academic impact, for papers by Helen Stewart Breakdown of academic impact, for papers by Shivanand R. Patil Breakdown of academic impact, for papers by Vazken M. Der Kaloustian Breakdown of academic impact, for papers by Mohnish Suri Breakdown of academic impact, for papers by Jennifer A. Donald Breakdown of academic impact, for papers by Dvorah Abeliovich Breakdown of academic impact, for papers by Ruth Newbury‐Ecob Breakdown of academic impact, for papers by Stefan J. White
Rankless by CCL
2026