Leah W. Burke

1.2k total citations
22 papers, 552 citations indexed

About

Leah W. Burke is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Leah W. Burke has authored 22 papers receiving a total of 552 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 7 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Leah W. Burke's work include Genomics and Rare Diseases (4 papers), Prenatal Screening and Diagnostics (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Leah W. Burke is often cited by papers focused on Genomics and Rare Diseases (4 papers), Prenatal Screening and Diagnostics (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Leah W. Burke collaborates with scholars based in United States, Australia and Germany. Leah W. Burke's co-authors include Marilyn C. Jones, Gregory B. Russell, Matthew J. McGinniss, David Brown, Jeffrey L. Deaton, James T. Mascarello, April T. Davenport, Jürgen Kohlhase, Angela E. Scheuerle and Joan M. Stoler and has published in prestigious journals such as Nucleic Acids Research, PEDIATRICS and Kidney International.

In The Last Decade

Leah W. Burke

21 papers receiving 537 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Leah W. Burke United States 13 247 182 105 74 53 22 552
Joy B. Redman United States 17 203 0.8× 301 1.7× 51 0.5× 71 1.0× 31 0.6× 27 781
Helen Fryssira Greece 16 278 1.1× 312 1.7× 46 0.4× 45 0.6× 55 1.0× 39 600
Seher Başaran Türkiye 17 305 1.2× 278 1.5× 149 1.4× 215 2.9× 90 1.7× 73 814
Thomas A. Maher United States 13 147 0.6× 270 1.5× 33 0.3× 58 0.8× 112 2.1× 23 586
Chin‐To Fong United States 11 197 0.8× 282 1.5× 138 1.3× 65 0.9× 35 0.7× 22 738
Olaf Rittinger Austria 17 384 1.6× 433 2.4× 21 0.2× 81 1.1× 66 1.2× 40 785
María A. Ramos‐Arroyo Spain 12 163 0.7× 281 1.5× 195 1.9× 61 0.8× 41 0.8× 27 556
Kyriaki S. Alatzoglou United Kingdom 15 327 1.3× 334 1.8× 37 0.4× 105 1.4× 114 2.2× 23 821
Alicia S. Martínez Argentina 10 256 1.0× 238 1.3× 43 0.4× 75 1.0× 40 0.8× 16 582
J. Amos United States 12 189 0.8× 273 1.5× 25 0.2× 105 1.4× 93 1.8× 21 814

Countries citing papers authored by Leah W. Burke

Since Specialization
Citations

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

Fields of papers citing papers by Leah W. Burke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leah W. Burke. 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 Leah W. Burke. The network helps show where Leah W. Burke may publish in the future.

Co-authorship network of co-authors of Leah W. Burke

This figure shows the co-authorship network connecting the top 25 collaborators of Leah W. Burke. A scholar is included among the top collaborators of Leah W. Burke 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 Leah W. Burke. Leah W. Burke 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.
Tinkle, Brad T., Ronald V. Lacro, & Leah W. Burke. (2023). Health Supervision for Children and Adolescents With Marfan Syndrome. PEDIATRICS. 151(4). 1 indexed citations
2.
Chambers, Christina, Diana L. Johnson, Ronghui Xu, et al.. (2021). Birth Outcomes in Women Who Have Taken Hydroxycholoroquine During Pregnancy: A Prospective Cohort Study. Arthritis & Rheumatology. 74(4). 711–724. 24 indexed citations
3.
Burke, Leah W., et al.. (2021). Two Cases of Preaxial Polydactyly of the Foot: Important Implications for Plastic Surgeons. Plastic & Reconstructive Surgery Global Open. 9(2). e3358–e3358. 1 indexed citations
4.
Cohen, Jennifer L., Samantha A. Schrier Vergano, Alanna Strong, et al.. (2020). EP300‐related Rubinstein–Taybi syndrome: Highlighted rare phenotypic findings and a genotype–phenotype meta‐analysis of 74 patients. American Journal of Medical Genetics Part A. 182(12). 2926–2938. 18 indexed citations
5.
McGregor, Tracy L., Susan A. Berry, Katrina M. Dipple, et al.. (2020). Management Principles for Acute Illness in Patients With Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency. PEDIATRICS. 147(1). 2 indexed citations
6.
Miller, David T., Debra Freedenberg, Elizabeth K. Schorry, et al.. (2019). Health Supervision for Children With Neurofibromatosis Type 1. PEDIATRICS. 143(5). 117 indexed citations
7.
Szelinger, Szabolcs, Newell Belnap, Keri Ramsey, et al.. (2019). Utilizing RNA and outlier analysis to identify an intronic splice‐altering variant inAP4S1in a sibling pair with progressive spastic paraplegia. Human Mutation. 41(2). 412–419. 5 indexed citations
8.
Covington, Jeffrey D., et al.. (2018). Tissue Specificity in Trisomy 22 Mosaicism: A Tale of Caution for Interpretation of Chromosomal Microarray Results.. PubMed. 44(4). 137–140. 1 indexed citations
9.
Burke, Leah W., et al.. (2014). Pai syndrome: median cleft lip, corpus callosum lipoma, and fibroepithelial skin tag.. PubMed. 14. ic7–ic7. 4 indexed citations
10.
Moeschler, John B., Roberto Amato, Leah W. Burke, et al.. (2009). Improving genetic health care: A Northern New England pilot project addressing the genetic evaluation of the child with developmental delays or intellectual disability. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 151C(3). 241–254. 13 indexed citations
11.
Borozdin, Wiktor, John M. Graham, Detlef Böhm, et al.. (2007). Multigene deletions on chromosome 20q13.13-q13.2 includingSALL4 result in an expanded phenotype of Okihiro syndrome plus developmental delay. Human Mutation. 28(8). 830–830. 42 indexed citations
12.
Simon, John W., et al.. (2007). Familial unilateral ectopia lentis. Journal of American Association for Pediatric Ophthalmology and Strabismus. 11(6). 620–621.
13.
Botzenhart, Elke, Andrew Green, Helena G. Ilyina, et al.. (2005). SALL1 mutation analysis in Townes-Brocks syndrome: twelve novel mutations and expansion of the phenotype. Human Mutation. 26(3). 282–282. 48 indexed citations
14.
Adam, Margaret P, Raoul C. M. Hennekam, Laura Davis Keppen, et al.. (2005). Marshall–Smith syndrome: Natural history and evidence of an osteochondrodysplasia with connective tissue abnormalities. American Journal of Medical Genetics Part A. 137A(2). 117–124. 29 indexed citations
15.
Vats, Abhay, Michael L. Moritz, Demetrius Ellis, et al.. (2003). Steroid-resistant nephrotic syndrome and congenital anomalies of kidneys: Evidence of locus on chromosome 13q. Kidney International. 64(1). 17–24. 14 indexed citations
16.
Burke, Leah W., April T. Davenport, Gregory B. Russell, & Jeffrey L. Deaton. (2000). Predictors of success after embryo transfer: Experience from a single provider. American Journal of Obstetrics and Gynecology. 182(5). 1001–1004. 38 indexed citations
17.
McGinniss, Matthew J., David Brown, Leah W. Burke, James T. Mascarello, & Marilyn C. Jones. (1997). Ring chromosome X in a child with manifestations of Kabuki syndrome. American Journal of Medical Genetics. 70(1). 37–42. 4 indexed citations
18.
19.
Burke, Leah W. & Marilyn C. Jones. (1995). Kabuki Syndrome: Underdiagnosed Recognizable Pattern in Cleft Palate Patients. The Cleft Palate-Craniofacial Journal. 32(1). 77–84. 57 indexed citations
20.
Klapholz, Henry & Leah W. Burke. (1975). Intrauterine fetal demise with a negative oxytocin challenge test.. PubMed. 15(4). 169–70. 2 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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