Lee Zellmer

1.4k total citations
8 papers, 257 citations indexed

About

Lee Zellmer is a scholar working on Genetics, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Lee Zellmer has authored 8 papers receiving a total of 257 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Lee Zellmer's work include Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomic variations and chromosomal abnormalities (2 papers). Lee Zellmer is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomic variations and chromosomal abnormalities (2 papers). Lee Zellmer collaborates with scholars based in United States. Lee Zellmer's co-authors include Isabelle Thiffault, Neil Miller, Carol Saunders, Emily Farrow, Laurie D. Smith, Stephen F. Kingsmore, Sarah Soden, Nathaly M. Sweeney, Laurel K. Willig and Narayanan Veeraraghavan and has published in prestigious journals such as Genetics in Medicine, Journal of Molecular Diagnostics and American Journal of Medical Genetics Part A.

In The Last Decade

Lee Zellmer

8 papers receiving 254 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lee Zellmer United States	7	203	88	39	32	28	8	257
Alison Yeung Australia	11	283 1.4×	130 1.5×	29 0.7×	69 2.2×	22 0.8×	19	385
Philip L. Beales United Kingdom	7	152 0.7×	102 1.2×	18 0.5×	32 1.0×	48 1.7×	8	263
Joshua L. Deignan United States	7	155 0.8×	79 0.9×	27 0.7×	15 0.5×	18 0.6×	8	249
Tomi L. Toler United States	7	139 0.7×	105 1.2×	23 0.6×	50 1.6×	58 2.1×	10	275
Rungnapa Ittiwut Thailand	10	83 0.4×	85 1.0×	17 0.4×	21 0.7×	9 0.3×	26	213
Emily C. Lisi United States	13	182 0.9×	142 1.6×	11 0.3×	65 2.0×	30 1.1×	22	411
M. Elizabeth McCready Canada	10	120 0.6×	80 0.9×	22 0.6×	39 1.2×	9 0.3×	25	254
Mariam AlMulla Qatar	7	125 0.6×	92 1.0×	17 0.4×	31 1.0×	11 0.4×	7	280
Stefano Petrocchi Italy	8	129 0.6×	84 1.0×	16 0.4×	16 0.5×	16 0.6×	15	236
Jillene Kogan United States	9	94 0.5×	105 1.2×	29 0.7×	34 1.1×	20 0.7×	13	217

Countries citing papers authored by Lee Zellmer

Since Specialization

Citations

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

Fields of papers citing papers by Lee Zellmer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lee Zellmer

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

All Works

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8 of 8 papers shown

Cadieux‐Dion, Maxime, Byunggil Yoo, Neil Miller, et al.. (2021). Factors Affecting Migration to GRCh38 in Laboratories Performing Clinical Next-Generation Sequencing. Journal of Molecular Diagnostics. 23(5). 651–657. 12 indexed citations

Thiffault, Isabelle, Andrea M. Atherton, Bryce A. Heese, et al.. (2020). Pathogenic variants in KPTN gene identified by clinical whole-genome sequencing. Molecular Case Studies. 6(3). a003970–a003970. 4 indexed citations

Thiffault, Isabelle, Emily Farrow, Lee Zellmer, et al.. (2018). Clinical genome sequencing in an unbiased pediatric cohort. Genetics in Medicine. 21(2). 303–310. 31 indexed citations

Cadieux‐Dion, Maxime, Nicole P. Safina, Kendra Engleman, et al.. (2018). Novel heterozygous pathogenic variants in CHUK in a patient with AEC-like phenotype, immune deficiencies and 1q21.1 microdeletion syndrome: a case report. BMC Medical Genetics. 19(1). 41–41. 6 indexed citations

Petrikin, Josh E, Julie A. Cakici, Michelle M. Clark, et al.. (2018). The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants. npj Genomic Medicine. 3(1). 6–6. 137 indexed citations

Thiffault, Isabelle, Britton Zuccarelli, Xuan Yuan, et al.. (2017). Hypotonia and intellectual disability without dysmorphic features in a patient with PIGN-related disease. BMC Medical Genetics. 18(1). 124–124. 11 indexed citations

Thiffault, Isabelle, Emily Farrow, Laurie D. Smith, et al.. (2016). PCDH19‐related epileptic encephalopathy in a male mosaic for a truncating variant. American Journal of Medical Genetics Part A. 170(6). 1585–1589. 34 indexed citations

Thiffault, Isabelle, Carol Saunders, Nikita Raje, et al.. (2015). A patient with polymerase E1 deficiency (POLE1): clinical features and overlap with DNA breakage/instability syndromes. BMC Medical Genetics. 16(1). 31–31. 22 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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