Lisa E. Esterling

1.3k total citations
16 papers, 1.0k citations indexed

About

Lisa E. Esterling is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Lisa E. Esterling has authored 16 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Psychiatry and Mental health. Recurrent topics in Lisa E. Esterling's work include Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (4 papers) and BRCA gene mutations in cancer (4 papers). Lisa E. Esterling is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (4 papers) and BRCA gene mutations in cancer (4 papers). Lisa E. Esterling collaborates with scholars based in United States and Netherlands. Lisa E. Esterling's co-authors include Takeo Yoshikawa, Gordon Turner, Sevilla D. Detera‐Wadleigh, Elliot S. Gershon, Susan Manley, Wade H. Berrettini, Jayaprakash D. Karkera, Krystal Brown, Theodora S. Ross and S D Detera-Wadleigh and has published in prestigious journals such as Proceedings of the National Academy of Sciences, JAMA and Molecular Microbiology.

In The Last Decade

Lisa E. Esterling

16 papers receiving 993 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lisa E. Esterling United States	13	665	388	215	137	133	16	1.0k
Eric Strengman Netherlands	18	518 0.8×	739 1.9×	84 0.4×	82 0.6×	64 0.5×	27	1.3k
Dimitri J. Stavropoulos Canada	23	1.2k 1.8×	731 1.9×	129 0.6×	55 0.4×	156 1.2×	66	1.7k
Koen L.I. van Gassen Netherlands	22	407 0.6×	564 1.5×	133 0.6×	319 2.3×	68 0.5×	42	1.3k
Kimberly Chambert United States	10	704 1.1×	509 1.3×	64 0.3×	102 0.7×	134 1.0×	10	1.1k
Hooshang Lahooti Australia	14	749 1.1×	547 1.4×	64 0.3×	63 0.5×	46 0.3×	32	1.1k
Carol Guy United Kingdom	16	257 0.4×	522 1.3×	70 0.3×	169 1.2×	65 0.5×	25	910
Mina Ohadi Iran	18	270 0.4×	525 1.4×	97 0.5×	197 1.4×	45 0.3×	73	1.0k
Cheryl Shoubridge Australia	20	748 1.1×	726 1.9×	79 0.4×	161 1.2×	56 0.4×	49	1.3k
Bhooma Thiruvahindrapuram Canada	14	500 0.8×	420 1.1×	92 0.4×	61 0.4×	74 0.6×	47	880
Alisa M. Goldstein United States	13	317 0.5×	350 0.9×	84 0.4×	42 0.3×	103 0.8×	19	992

Countries citing papers authored by Lisa E. Esterling

Since Specialization

Citations

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

Fields of papers citing papers by Lisa E. Esterling

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lisa E. Esterling

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

All Works

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16 of 16 papers shown

Esterling, Lisa E., Krystal Brown, Brian Morris, et al.. (2020). Impact of a Cancer Gene Variant Reclassification Program Over a 20-Year Period. JCO Precision Oncology. 4(4). 944–954. 38 indexed citations

Mersch, Jacqueline, Sara Pirzadeh‐Miller, Erin Mundt, et al.. (2018). Prevalence of Variant Reclassification Following Hereditary Cancer Genetic Testing. JAMA. 320(12). 1266–1266. 175 indexed citations

Pruss, Dmitry, Brian Morris, Elisha Hughes, et al.. (2014). Development and validation of a new algorithm for the reclassification of genetic variants identified in the BRCA1 and BRCA2 genes. Breast Cancer Research and Treatment. 147(1). 119–132. 33 indexed citations

Eggington, Julie M., Karla R. Bowles, Susan Manley, et al.. (2013). A comprehensive laboratory‐based program for classification of variants of uncertain significance in hereditary cancer genes. Clinical Genetics. 86(3). 229–237. 140 indexed citations

Yoshikawa, Takeo, Muralidhara Padigaru, Jayaprakash D. Karkera, et al.. (2000). Genomic structure and novel variants of myo-inositol monophosphatase 2 (IMPA2). Molecular Psychiatry. 5(2). 165–171. 39 indexed citations

Guan, Xin‐Yuan, Eric D. Green, Rob Nicolson, et al.. (2000). Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: Identification of a BAC contig spanning the translocation breakpoint at 7q21. American Journal of Medical Genetics. 96(6). 749–753. 38 indexed citations

Detera‐Wadleigh, Sevilla D., Judith A. Badner, Wade H. Berrettini, et al.. (1999). A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2. Proceedings of the National Academy of Sciences. 96(10). 5604–5609. 322 indexed citations

Yoshikawa, Takeo, et al.. (1998). Multiple Transcriptional Variants and RNA Editing inC18orf1,a Novel Gene with LDLRA and Transmembrane Domains on 18p11.2. Genomics. 47(2). 246–257. 13 indexed citations

Esterling, Lisa E., Takeo Yoshikawa, Gordon Turner, et al.. (1998). Serotonin transporter (5‐HTT) gene and bipolar affective disorder. American Journal of Medical Genetics. 81(1). 37–40. 2 indexed citations

10.

Esterling, Lisa E., Takeo Yoshikawa, Gordon Turner, et al.. (1998). Serotonin transporter (5-HTT) gene and bipolar affective disorder. American Journal of Medical Genetics. 81(1). 37–40. 48 indexed citations

11.

Esterling, Lisa E., Takeo Yoshikawa, Gordon Turner, et al.. (1998). Serotonin transporter (5-HTT) gene and bipolar affective disorder.. PubMed. 81(1). 37–40. 54 indexed citations

12.

Engelen, J.J.M., et al.. (1997). Assignment of the Human Gene for Smoothelin (SMTN) to Chromosome 22q12 by Fluorescence in Situ Hybridization and Radiation Hybrid Mapping. Genomics. 43(2). 245–247. 12 indexed citations

13.

Esterling, Lisa E., Tara C. Matise, Alan R. Sanders, et al.. (1997). An integrated physical map of 18p11.2: a susceptibility region for bipolar disorder. Molecular Psychiatry. 2(6). 501–504. 10 indexed citations

14.

Yoshikawa, Takeo, Lisa E. Esterling, Joan Overhauser, et al.. (1997). Isolation of chromosome 18-specific brain transcripts as positional candidates for bipolar disorder. American Journal of Medical Genetics. 74(2). 140–149. 14 indexed citations

15.

Yoshikawa, Takeo, et al.. (1997). A novel human myo-inositol monophosphatase gene, IMP.18p, maps to a susceptibility region for bipolar disorder. Molecular Psychiatry. 2(5). 393–397. 44 indexed citations

16.

Esterling, Lisa E. & Nicholas Delihas. (1994). The regulatory RNA gene micF is present in several species of Gram‐negative bacteria and is phylogenetically conserved. Molecular Microbiology. 12(4). 639–646. 33 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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