Emily Groopman

2.3k total citations
16 papers, 381 citations indexed

About

Emily Groopman is a scholar working on Molecular Biology, Genetics and Nephrology. According to data from OpenAlex, Emily Groopman has authored 16 papers receiving a total of 381 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Nephrology. Recurrent topics in Emily Groopman's work include Renal Diseases and Glomerulopathies (7 papers), Genomics and Rare Diseases (6 papers) and Renal and related cancers (5 papers). Emily Groopman is often cited by papers focused on Renal Diseases and Glomerulopathies (7 papers), Genomics and Rare Diseases (6 papers) and Renal and related cancers (5 papers). Emily Groopman collaborates with scholars based in United States, Canada and Lebanon. Emily Groopman's co-authors include Ali G. Gharavi, Hila Milo Rasouly, Rachel N. Carmody, Richard W. Wrangham, Thomas Hays, David B. Goldstein, Wendy K. Chung, Chunhua Weng, Gundula Povysil and David Fasel and has published in prestigious journals such as SHILAP Revista de lepidopterología, Annals of Internal Medicine and Kidney International.

In The Last Decade

Emily Groopman

13 papers receiving 375 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Emily Groopman United States	9	190	154	139	41	30	16	381
Garðar Sveinbjörnsson Iceland	9	184 1.0×	75 0.5×	146 1.1×	45 1.1×	23 0.8×	9	477
Jiao Qiao China	10	180 0.9×	61 0.4×	16 0.1×	10 0.2×	5 0.2×	32	313
Diptavo Dutta United States	8	111 0.6×	17 0.1×	153 1.1×	10 0.2×	4 0.1×	17	291
Roberto Semeraro Italy	10	200 1.1×	27 0.2×	59 0.4×	10 0.2×	6 0.2×	23	351
Suzanne K. Cordovado United States	11	93 0.5×	48 0.3×	155 1.1×	35 0.9×	1 0.0×	23	391
Haoran Xue United States	9	144 0.8×	8 0.1×	178 1.3×	10 0.2×	10 0.3×	22	336
Petteri Ahtiainen Finland	11	106 0.6×	75 0.5×	160 1.2×	14 0.3×		17	388
Giuseppina Casu Italy	8	96 0.5×	46 0.3×	192 1.4×	38 0.9×	1 0.0×	13	325
Kyoko Kanda Japan	10	214 1.1×	95 0.6×	47 0.3×	7 0.2×		19	345
Nam Pho United States	5	215 1.1×	7 0.0×	95 0.7×	11 0.3×	18 0.6×	6	418

Countries citing papers authored by Emily Groopman

Since Specialization

Citations

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

Fields of papers citing papers by Emily Groopman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emily Groopman

This figure shows the co-authorship network connecting the top 25 collaborators of Emily Groopman. A scholar is included among the top collaborators of Emily Groopman 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 Emily Groopman. Emily Groopman 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

Goldstein, Jennifer, Amanda Thomas‐Wilson, Emily Groopman, et al.. (2024). ClinGen variant curation expert panel recommendations for classification of variants in GAMT, GATM and SLC6A8 for cerebral creatine deficiency syndromes. Molecular Genetics and Metabolism. 142(1). 108362–108362. 4 indexed citations

Mew, Nicholas Ah, Ljubica Caldovic, Annette Feigenbaum, et al.. (2024). P007: PP4 criteria specifications for proximal urea cycle disorders*. SHILAP Revista de lepidopterología. 2. 100884–100884.

Goldstein, Jennifer, Emily Groopman, Shruthi Mohan, et al.. (2024). Developing a scoring system for gene curation prioritization in lysosomal diseases. Molecular Genetics and Metabolism. 143(1-2). 108572–108572.

Groopman, Emily, Shruthi Mohan, Raquel Fernández, et al.. (2024). Assessment of genes involved in lysosomal diseases using the ClinGen clinical validity framework. Molecular Genetics and Metabolism. 143(3). 108593–108593.

Groopman, Emily & Hila Milo Rasouly. (2024). Navigating Genetic Testing in Nephrology: Options and Decision-Making Strategies. Kidney International Reports. 10(3). 673–695. 1 indexed citations

Caldovic, Ljubica, William Craigen, Annette Feigenbaum, et al.. (2023). CURATION OF SEQUENCE VARIANTS IN UREA CYCLE GENES. Molecular Genetics and Metabolism. 138(3). 107488–107488. 1 indexed citations

Groopman, Emily, Gundula Povysil, David B. Goldstein, & Ali G. Gharavi. (2020). Rare genetic causes of complex kidney and urological diseases. Nature Reviews Nephrology. 16(11). 641–656. 25 indexed citations

Hays, Thomas, Emily Groopman, & Ali G. Gharavi. (2020). Genetic testing for kidney disease of unknown etiology. Kidney International. 98(3). 590–600. 35 indexed citations

Li, Yifu, Emily Groopman, Vivette D. D’Agati, et al.. (2020). Type IV Collagen Mutations in Familial IgA Nephropathy. Kidney International Reports. 5(7). 1075–1078. 26 indexed citations

10.

Batal, Ibrahim, et al.. (2018). Unusual Case of Lipoprotein Glomerulopathy First Diagnosed in a Protocol Kidney Allograft Biopsy. Kidney International Reports. 4(2). 350–354. 8 indexed citations

11.

Groopman, Emily, Hila Milo Rasouly, & Ali G. Gharavi. (2018). Genomic medicine for kidney disease. Nature Reviews Nephrology. 14(2). 83–104. 79 indexed citations

12.

Xie, Gangcai, Chi Yuan, Ziran Li, et al.. (2018). Deep Phenotyping on Electronic Health Records Facilitates Genetic Diagnosis by Clinical Exomes. The American Journal of Human Genetics. 103(1). 58–73. 79 indexed citations

13.

Rasouly, Hila Milo, Emily Groopman, David Fasel, et al.. (2018). The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing. Annals of Internal Medicine. 170(1). 11–21. 46 indexed citations

14.

Nestor, Jordan G., Emily Groopman, & Ali G. Gharavi. (2017). Towards precision nephrology: the opportunities and challenges of genomic medicine. Journal of Nephrology. 31(1). 47–60. 11 indexed citations

15.

Carmody, Rachel N., Michael Dannemann, Adrian W. Briggs, et al.. (2016). Genetic Evidence of Human Adaptation to a Cooked Diet. Genome Biology and Evolution. 8(4). 1091–1103. 21 indexed citations

16.

Groopman, Emily, Rachel N. Carmody, & Richard W. Wrangham. (2014). Cooking increases net energy gain from a lipid‐rich food. American Journal of Physical Anthropology. 156(1). 11–18. 45 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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