Leah Fleming

492 total citations
5 papers, 128 citations indexed

About

Leah Fleming is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Leah Fleming has authored 5 papers receiving a total of 128 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 1 paper in Genetics. Recurrent topics in Leah Fleming's work include Genomics and Rare Diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Renal and related cancers (2 papers). Leah Fleming is often cited by papers focused on Genomics and Rare Diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Renal and related cancers (2 papers). Leah Fleming collaborates with scholars based in United States, Germany and Lebanon. Leah Fleming's co-authors include Thierry Vilboux, Julie Hoover‐Fong, Ronald D. Cohn, Roxanne Fischer, Kailash Daryanani, Joann Bodurtha, May Christine V. Malicdan, Weiyi Mu, William A. Gahl and David R. Murdock and has published in prestigious journals such as Clinical Journal of the American Society of Nephrology, Human Mutation and American Journal of Medical Genetics Part A.

In The Last Decade

Leah Fleming

5 papers receiving 127 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Leah Fleming United States	5	78	74	27	19	17	5	128
Zandrè Bruwer Oman	7	52 0.7×	52 0.7×	24 0.9×	25 1.3×	14 0.8×	19	149
Natalya Karp Canada	8	53 0.7×	46 0.6×	15 0.6×	21 1.1×	10 0.6×	14	134
Samantha Penney United States	5	68 0.9×	76 1.0×	14 0.5×	10 0.5×	11 0.6×	5	157
Dominik S. Westphal Germany	7	82 1.1×	51 0.7×	19 0.7×	9 0.5×	22 1.3×	29	159
Haruka Hamanoue Japan	10	118 1.5×	84 1.1×	33 1.2×	13 0.7×	32 1.9×	23	220
Elaine M. Pereira United States	8	68 0.9×	100 1.4×	35 1.3×	7 0.4×	15 0.9×	24	191
Bianca Russell United States	7	77 1.0×	71 1.0×	20 0.7×	13 0.7×	11 0.6×	18	142
Berardo Rinaldi Italy	7	99 1.3×	90 1.2×	15 0.6×	9 0.5×	12 0.7×	26	170
Jillene Kogan United States	9	105 1.3×	94 1.3×	34 1.3×	18 0.9×	10 0.6×	13	217
Bekir Ergüner Türkiye	7	78 1.0×	68 0.9×	10 0.4×	10 0.5×	8 0.5×	14	162

Countries citing papers authored by Leah Fleming

Since Specialization

Citations

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

Fields of papers citing papers by Leah Fleming

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Leah Fleming

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

All Works

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5 of 5 papers shown

1.

Vocke, Cathy D., Leah Fleming, Ali Amin, et al.. (2022). A diagnosis of Birt–Hogg–Dubé syndrome in individuals with Smith–Magenis syndrome: Recommendation for cancer screening. American Journal of Medical Genetics Part A. 191(2). 490–497. 8 indexed citations

2.

Ballout, Rami A., Myra Wick, Siddharth Srivastava, et al.. (2020). Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features. Human Mutation. 41(7). 1238–1249. 10 indexed citations

3.

Fleming, Leah, Daniel Doherty, Melissa A. Parisi, et al.. (2017). Prospective Evaluation of Kidney Disease in Joubert Syndrome. Clinical Journal of the American Society of Nephrology. 12(12). 1962–1973. 49 indexed citations

4.

Telegrafi, Aida, Bryn D. Webb, Carlos E. Speck‐Martins, et al.. (2017). Identification of STAC3 variants in non‐Native American families with overlapping features of Carey–Fineman–Ziter syndrome and Moebius syndrome. American Journal of Medical Genetics Part A. 173(10). 2763–2771. 27 indexed citations

5.

Fleming, Leah, Monica E. Lemmon, Weiyi Mu, et al.. (2015). Genotype–phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/PIGN‐related epilepsy. American Journal of Medical Genetics Part A. 170(1). 77–86. 34 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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