Gayle H. Tyerman

677 total citations
14 papers, 498 citations indexed

About

Gayle H. Tyerman is a scholar working on Rheumatology, Surgery and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Gayle H. Tyerman has authored 14 papers receiving a total of 498 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Rheumatology, 6 papers in Surgery and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Gayle H. Tyerman's work include Folate and B Vitamins Research (6 papers), Congenital Anomalies and Fetal Surgery (4 papers) and Prenatal Screening and Diagnostics (4 papers). Gayle H. Tyerman is often cited by papers focused on Folate and B Vitamins Research (6 papers), Congenital Anomalies and Fetal Surgery (4 papers) and Prenatal Screening and Diagnostics (4 papers). Gayle H. Tyerman collaborates with scholars based in United States and Canada. Gayle H. Tyerman's co-authors include Hope Northrup, Jack Μ. Fletcher, Kit Sing Au, Susan H. Blanton, Kelly A. Volcik, Alanna C. Morrison, Irene Townsend, Christina M. Davidson, Nadia Verbruggen and Dennis P. Grogan and has published in prestigious journals such as Blood, The Journal of Clinical Endocrinology & Metabolism and American Journal of Obstetrics and Gynecology.

In The Last Decade

Gayle H. Tyerman

14 papers receiving 473 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gayle H. Tyerman United States 12 219 172 145 143 97 14 498
Patrick G. Brosnan United States 13 50 0.2× 106 0.6× 97 0.7× 100 0.7× 174 1.8× 24 575
Susan J. McAllion United Kingdom 12 146 0.7× 394 2.3× 104 0.7× 51 0.4× 54 0.6× 15 504
Amnon Cohen Italy 11 29 0.1× 147 0.9× 178 1.2× 129 0.9× 178 1.8× 16 745
Ulpu Seppänen Finland 11 115 0.5× 131 0.8× 357 2.5× 112 0.8× 104 1.1× 20 700
Hakan Çoksüer Türkiye 16 108 0.5× 25 0.1× 80 0.6× 90 0.6× 89 0.9× 45 754
Nadine Lucidarme France 10 28 0.1× 88 0.5× 61 0.4× 73 0.5× 78 0.8× 14 372
Emma Bertucci Italy 14 66 0.3× 45 0.3× 287 2.0× 80 0.6× 193 2.0× 55 884
Pierangela De Biasio Italy 17 38 0.2× 55 0.3× 418 2.9× 216 1.5× 134 1.4× 44 738
Harry Pachajoa Colombia 11 42 0.2× 176 1.0× 60 0.4× 106 0.7× 128 1.3× 149 495
Monica Grover United States 11 67 0.3× 167 1.0× 30 0.2× 45 0.3× 118 1.2× 20 388

Countries citing papers authored by Gayle H. Tyerman

Since Specialization
Citations

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

Fields of papers citing papers by Gayle H. Tyerman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gayle H. Tyerman. 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 Gayle H. Tyerman. The network helps show where Gayle H. Tyerman may publish in the future.

Co-authorship network of co-authors of Gayle H. Tyerman

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

All Works

14 of 14 papers shown
1.
Northrup, Hope, Alanna C. Morrison, Christina M. Davidson, et al.. (2012). Association of copper‐zinc superoxide dismutase (SOD1) and manganese superoxide dismutase (SOD2) genes with nonsyndromic myelomeningocele. Birth Defects Research Part A Clinical and Molecular Teratology. 94(10). 762–769. 21 indexed citations
2.
Dobbs, Kerry, Amma Bosompem, Elaine Coustan‐Smith, et al.. (2011). Agammaglobulinemia associated with BCR− B cells and enhanced expression of CD19. Blood. 118(7). 1828–1837. 10 indexed citations
3.
Au, Kit Sing, et al.. (2010). Association of retinoic acid receptor genes with meningomyelocele. Birth Defects Research Part A Clinical and Molecular Teratology. 91(1). 39–43. 13 indexed citations
4.
Ward, Leanne M., Frank Rauch, Michael P. Whyte, et al.. (2010). Alendronate for the Treatment of Pediatric Osteogenesis Imperfecta: A Randomized Placebo-Controlled Study. The Journal of Clinical Endocrinology & Metabolism. 96(2). 355–364. 151 indexed citations
5.
Au, Kit Sing, Alanna C. Morrison, Jack Μ. Fletcher, et al.. (2010). Association of folate receptor (folr1, folr2, folr3) and reduced folate carrier (slc19a1) genes with meningomyelocele. Birth Defects Research Part A Clinical and Molecular Teratology. 88(8). 689–694. 35 indexed citations
6.
Northrup, Hope, et al.. (2009). Genetic association study of putative functional single nucleotide polymorphisms of genes in folate metabolism and spina bifida. American Journal of Obstetrics and Gynecology. 201(4). 394.e1–394.e11. 41 indexed citations
7.
Davidson, Christina M., Hope Northrup, Terri M. King, et al.. (2008). Genes in Glucose Metabolism and Association With Spina Bifida. Reproductive Sciences. 15(1). 51–58. 37 indexed citations
8.
Au, Kit Sing, Alanna C. Morrison, Paul T. Cirino, et al.. (2008). Characteristics of a spina bifida population including North American Caucasian and Hispanic individuals. Birth Defects Research Part A Clinical and Molecular Teratology. 82(10). 692–700. 28 indexed citations
9.
King, Terri M., Kit Sing Au, Christina M. Davidson, et al.. (2007). The Impact of BRCA1 on Spina Bifida Meningomyelocele Lesions. Annals of Human Genetics. 71(6). 719–728. 10 indexed citations
10.
Tyerman, Gayle H., et al.. (2007). Apoptotic Gene Analysis in Idiopathic Talipes Equinovarus (Clubfoot). Clinical Orthopaedics and Related Research. 462. 32–37. 30 indexed citations
11.
Au, Kit Sing, Hope Northrup, Kelly A. Volcik, et al.. (2005). Promotor genotype of the platelet‐derived growth factor receptor‐α gene shows population stratification but not association with spina bifida meningomyelocele. American Journal of Medical Genetics Part A. 139A(3). 194–198. 17 indexed citations
12.
Volcik, Kelly A., Susan H. Blanton, Mark Kruzel, et al.. (2002). Testing for genetic associations with the PAX gene family in a spina bifida population. American Journal of Medical Genetics. 110(3). 195–202. 18 indexed citations
13.
Volcik, Kelly A., Susan H. Blanton, Mark Kruzel, et al.. (2002). Testing for genetic associations in a spina bifida population: Analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defects. American Journal of Medical Genetics. 110(3). 203–207. 24 indexed citations
14.
Volcik, Kelly A., et al.. (2000). Methylenetetrahydrofolate reductase and spina bifida: Evaluation of level of defect and maternal genotypic risk in Hispanics. American Journal of Medical Genetics. 95(1). 21–27. 63 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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