Lisa Edelmann

7.5k total citations
79 papers, 3.3k citations indexed

About

Lisa Edelmann is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Lisa Edelmann has authored 79 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Genetics, 44 papers in Molecular Biology and 11 papers in Plant Science. Recurrent topics in Lisa Edelmann's work include Genomic variations and chromosomal abnormalities (29 papers), Congenital heart defects research (17 papers) and Genomics and Rare Diseases (14 papers). Lisa Edelmann is often cited by papers focused on Genomic variations and chromosomal abnormalities (29 papers), Congenital heart defects research (17 papers) and Genomics and Rare Diseases (14 papers). Lisa Edelmann collaborates with scholars based in United States, France and Netherlands. Lisa Edelmann's co-authors include Ruth Kornreich, Robert J. Desnick, Bernice E. Morrow, Stuart A. Scott, Raj K. Pandita, Winfried Edelmann, Kurt Hirschhorn, Tracy Brandt, Ninette Cohen and Alan Shanske and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and PEDIATRICS.

In The Last Decade

Lisa Edelmann

77 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lisa Edelmann United States 31 1.8k 1.5k 374 370 370 79 3.3k
Marwan Shinawi United States 32 2.4k 1.3× 1.5k 1.0× 146 0.4× 226 0.6× 402 1.1× 137 4.3k
Cornelius F. Boerkoel United States 34 2.4k 1.3× 1.3k 0.9× 127 0.3× 172 0.5× 181 0.5× 129 4.2k
T. Mohandas United States 34 2.6k 1.4× 1.5k 1.0× 257 0.7× 81 0.2× 148 0.4× 65 3.9k
Marcia L. Budarf United States 34 2.9k 1.5× 1.5k 1.0× 392 1.0× 726 2.0× 798 2.2× 72 4.0k
Weizhen Ji United States 14 1.9k 1.0× 1.1k 0.7× 93 0.2× 198 0.5× 162 0.4× 47 3.3k
Bassem A. Bejjani United States 36 1.8k 1.0× 2.6k 1.8× 577 1.5× 143 0.4× 72 0.2× 83 4.1k
Sami A. Sanjad Lebanon 16 2.6k 1.4× 704 0.5× 105 0.3× 703 1.9× 105 0.3× 46 3.8k
Helle F. Jørgensen United Kingdom 27 3.8k 2.1× 687 0.5× 169 0.5× 275 0.7× 220 0.6× 41 4.9k
Heather E. Wheeler United States 24 1.5k 0.8× 1.2k 0.8× 103 0.3× 181 0.5× 74 0.2× 59 2.8k
Jeremy M. Simon United States 29 2.1k 1.1× 700 0.5× 148 0.4× 222 0.6× 132 0.4× 80 2.9k

Countries citing papers authored by Lisa Edelmann

Since Specialization
Citations

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

Fields of papers citing papers by Lisa Edelmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lisa Edelmann

This figure shows the co-authorship network connecting the top 25 collaborators of Lisa Edelmann. A scholar is included among the top collaborators of Lisa Edelmann 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 Lisa Edelmann. Lisa Edelmann 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.
Webb, Bryn D., D Corrigan, Lisong Shi, et al.. (2024). An algorithm to identify patients aged 0–3 with rare genetic disorders. Orphanet Journal of Rare Diseases. 19(1). 183–183.
2.
Webb, Bryn D., et al.. (2024). Familial RPL26 Variant Causing Congenital Anomalies Without Hematological Features of Diamond Blackfan Anemia. American Journal of Medical Genetics Part A. 197(5). e63954–e63954.
3.
Pratt, Victoria M., Erin C. Boone, Ulrich Broeckel, et al.. (2022). Characterization of Reference Materials for TPMT and NUDT15. Journal of Molecular Diagnostics. 24(10). 1079–1088. 11 indexed citations
4.
Singh, Ram J., Ana S.A. Cohen, Geetu Mendiratta, et al.. (2021). Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay. Molecular Case Studies. 7(3). a005991–a005991. 3 indexed citations
5.
Cai, Xiaoqiang, et al.. (2019). Clinical Genetic Testing for Fragile X Syndrome by Polymerase Chain Reaction Amplification and Southern Blot Analyses. Methods in molecular biology. 1942. 11–27. 2 indexed citations
6.
Zhang, Jinglan, Anastasia Fedick, Geping Zhao, et al.. (2016). Analytical Validation of a Personalized Medicine APOL1 Genotyping Assay for Nondiabetic Chronic Kidney Disease Risk Assessment. Journal of Molecular Diagnostics. 18(2). 260–266. 12 indexed citations
7.
Weisfeld‐Adams, James D., Lisa Edelmann, Inder Gadi, & Lakshmi Mehta. (2012). Phenotypic heterogeneity in a family with a small atypical microduplication of chromosome 22q11.2 involving TBX1. European Journal of Medical Genetics. 55(12). 732–736. 21 indexed citations
8.
Karakikes, Ioannis, Lisa Edelmann, Robert J. Desnick, et al.. (2010). Amniotic Fluid Cells Are More Efficiently Reprogrammed to Pluripotency Than Adult Cells. Cellular Reprogramming. 12(2). 117–125. 68 indexed citations
9.
Scott, Stuart A., Ninette Cohen, Tracy Brandt, et al.. (2010). Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization. Genetics in Medicine. 12(2). 85–92. 62 indexed citations
10.
Scott, Stuart A., Lisa Edelmann, Liu Liu, et al.. (2010). Experience with carrier screening and prenatal diagnosis for 16 Ashkenazi Jewish genetic diseases. Human Mutation. 31(11). 1240–1250. 115 indexed citations
11.
Balwani, Manisha, et al.. (2010). Type 1 Gaucher Disease. Archives of Internal Medicine. 170(16). 1463–9. 54 indexed citations
12.
Karakikes, Ioannis, Lisa Edelmann, Robert J. Desnick, et al.. (2009). Amniotic Fluid Cells Are More Efficiently Reprogrammed to Pluripotency Than Adult Cells. Cellular Reprogramming. 2863386655–2863386655. 10 indexed citations
13.
14.
Scherer, Stefan, M. Seifert, R. Hanselmann, et al.. (2006). 1[alpha],25‐dihydroxyvitamin D3enhances annexin II dependent proliferation of osteoblasts. Journal of Cellular Biochemistry. 100(3). 679–692. 6 indexed citations
15.
Edelmann, Lisa, Ghazala Hashmi, Yuhua Song, et al.. (2004). Cystic fibrosis carrier screening: Validation of a novel method using BeadChip technology. Genetics in Medicine. 6(5). 431–438. 14 indexed citations
16.
Kornreich, Ruth, Josef Ekstein, Lisa Edelmann, & Robert J. Desnick. (2004). Premarital and prenatal screening for cystic fibrosis: Experience in the Ashkenazi Jewish population. Genetics in Medicine. 6(5). 415–420. 21 indexed citations
17.
Edelmann, Lisa, Jianli Dong, Robert J. Desnick, & Ruth Kornreich. (2002). Carrier Screening for Mucolipidosis Type IV in the American Ashkenazi Jewish Population. The American Journal of Human Genetics. 70(4). 1023–1027. 30 indexed citations
18.
Edelmann, Lisa, Elizabeth Spiteri, Rosalie Goldberg, et al.. (1999). A Common Breakpoint on 11q23 in Carriers of the Constitutional t(11;22) Translocation. The American Journal of Human Genetics. 65(6). 1608–1616. 46 indexed citations
19.
Edelmann, Lisa, Raj K. Pandita, & Bernice E. Morrow. (1999). Low-Copy Repeats Mediate the Common 3-Mb Deletion in Patients with Velo-cardio-facial Syndrome. The American Journal of Human Genetics. 64(4). 1076–1086. 239 indexed citations
20.
Funke, Birgit, Bruno Saint-Jore, Anne Puech, et al.. (1997). Characterization and Mutation Analysis of Goosecoid-like (GSCL), a Homeodomain-Containing Gene That Maps to the Critical Region for VCFS/DGS on 22q11. Genomics. 46(3). 364–372. 21 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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