Andrea Gropman

12.3k total citations · 1 hit paper
200 papers, 5.1k citations indexed

About

Andrea Gropman is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Andrea Gropman has authored 200 papers receiving a total of 5.1k indexed citations (citations by other indexed papers that have themselves been cited), including 115 papers in Molecular Biology, 82 papers in Clinical Biochemistry and 75 papers in Genetics. Recurrent topics in Andrea Gropman's work include Metabolism and Genetic Disorders (82 papers), Mitochondrial Function and Pathology (59 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (30 papers). Andrea Gropman is often cited by papers focused on Metabolism and Genetic Disorders (82 papers), Mitochondrial Function and Pathology (59 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (30 papers). Andrea Gropman collaborates with scholars based in United States, Canada and United Kingdom. Andrea Gropman's co-authors include Carole Samango‐Sprouse, Marshall Summar, Teresa Sadeghin, Ann C. M. Smith, James V. Leonard, Mark L. Batshaw, Wallace C. Duncan, Donald W. Hadley, Matthew T. Whitehead and Sumit Parikh and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Molecular and Cellular Biology.

In The Last Decade

Andrea Gropman

188 papers receiving 5.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society

2014 372 citations Andrea Gropman, Lynne A. Wolfe et al. profile →

Peers

Countries citing papers authored by Andrea Gropman

Since Specialization

Citations

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

Fields of papers citing papers by Andrea Gropman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrea Gropman

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Incidence of miscarriages in women with children with 47,XXY, 48,XXXY, or 49,XXXXY 2025 ·Frontiers in Endocrinology ·(unknown), (unknown), Andrea Gropman, Teresa Sadeghin, Carole Samango‐Sprouse	0
2	SYNGAP1 Syndrome and the Brain Gene Registry 2025 ·Genes ·Maria Greco, Madhumita Chatterjee, (unknown), Andrea Gropman	3
3	P007: PP4 criteria specifications for proximal urea cycle disorders* 2024 ·SHILAP Revista de lepidopterología ·(unknown), Nicholas Ah Mew, Ljubica Caldovic, Annette Feigenbaum, (unknown), Emily Groopman, Andrea Gropman, Emily Kudalkar, Uta Lichter‐Konecki, (unknown), Elaine Spector, Meredith Weaver, Manya Warrier, Diane B. Zastrow, Amanda Thomas‐Wilson	0
4	Biallelic Variants in LIPT2 as a Cause of Infantile-Onset Dystonia: Expanding the Clinical and Molecular Spectrum 2024 ·Pediatric Neurology ·(unknown), Alonso Zea Vera, (unknown), Andrea Gropman, Parith Wongkittichote, Rebecca Ganetzky, Kaija J. Autio, Alexander J. Kastaniotis	1
5	Dysfunctional Postnatal Mitochondrial Energy Metabolism in a Patient with Neurodevelopmental Defects Caused by Intrauterine Growth Restriction Due to Idiopathic Placental Insufficiency 2024 ·International Journal of Molecular Sciences ·Martine Uittenbogaard, Andrea Gropman, Matthew T. Whitehead, Christine A. Brantner, (unknown), Anne Chiaramello	1
6	CURATION OF SEQUENCE VARIANTS IN UREA CYCLE GENES 2023 ·Molecular Genetics and Metabolism ·(unknown), (unknown), Ljubica Caldovic, William Craigen, Annette Feigenbaum, Raquel Fernández, Emily Groopman, Andrea Gropman, (unknown), (unknown), Uta Lichter‐Konecki, Sandesh C.S. Nagamani, Elaine Spector, Amanda Thomas‐Wilson, Manya Warrier, Meredith Weaver, Diane B. Zastrow	1
7	The functional impact of 1,570 individual amino acid substitutions in human OTC 2023 ·The American Journal of Human Genetics ·Russell S. Lo, Gareth A. Cromie, Michelle Tang, (unknown), (unknown), Amy Sirr, J. Nathan Kutz, Hiroki Morizono, Ljubica Caldovic, Nicholas Ah Mew, Andrea Gropman, Aimée M. Dudley	10
8	Gaps in Neurogenetics Education During Child Neurology Residency: Results of a National Survey 2022 ·Journal of Child Neurology ·(unknown), (unknown), (unknown), (unknown), Andrea Gropman	2
9	Review of Applications of Near-Infrared Spectroscopy in Two Rare Disorders with Executive and Neurological Dysfunction: UCD and PKU 2022 ·Genes ·(unknown), Wei-Liang Chen, Andrea Gropman	4
10	Integrated proteomic and metabolomic analyses of the mitochondrial neurodegenerative disease MELAS 2021 ·Molecular Omics ·Haorong Li, Martine Uittenbogaard, (unknown), (unknown), Andrea Gropman, Anne Chiaramello, Ling Hao	17
11	Management considerations for stroke-like episodes in MELAS with concurrent COVID-19 infection 2021 ·Journal of Neurology ·(unknown), Dana Harrar, Andrea Hahn, Elizabeth Wells, Andrea Gropman	7
12	Novel presentations associated with a PDHA1 variant – Alternating hemiplegia in Hemizygote proband and Guillain Barre Syndrome in Heterozygote mother 2021 ·European Journal of Paediatric Neurology ·(unknown), (unknown), Jirair K. Bedoyan, Andrea Gropman	3
13	Neurodevelopmental Outcome of Prenatally Diagnosed Boys With 47,XXY (Klinefelter Syndrome) and the Potential Influence of Early Hormonal Therapy 2021 ·Obstetrical & Gynecological Survey ·Carole Samango‐Sprouse, (unknown), Patricia C. Lasutschinkow, Teresa Sadeghin, (unknown), (unknown), Andrea Gropman	2
14	A novel frameshift mutation in SOX10 causes Waardenburg syndrome with peripheral demyelinating neuropathy, visual impairment and the absence of Hirschsprung disease 2020 ·American Journal of Medical Genetics Part A ·Elizabeth A. Burke, (unknown), Lynne A. Wolfe, Brian P. Brooks, John J. DiGiovanna, Donald W. Hadley, Tanya Lehky, Andrea Gropman, Cynthia J. Tifft, William A. Gahl, Camilo Toro, David R. Adams	7
15	Developing a New Set of ACGME Milestones for Child Neurology Residency 2020 ·Pediatric Neurology ·Dara V.F. Albert, Nancy Bass, John B. Bodensteiner, (unknown), Elizabeth S. Duke, (unknown), Andrea Gropman, Timothy Lotze, Jonathan W. Mink, (unknown), (unknown), David K. Urion, Laura Edgar	3
16	Expanding the phenotypic profile of Kleefstra syndrome: A female with low‐average intelligence and childhood apraxia of speech 2016 ·American Journal of Medical Genetics Part A ·Carole Samango‐Sprouse, Patrick Lawson, (unknown), Emily Stapleton, Teresa Sadeghin, Andrea Gropman	8
17	Delineating the spectrum of impairments, disabilities, and rehabilitation needs in methylmalonic acidemia (MMA) 2015 ·American Journal of Medical Genetics Part A ·(unknown), Scott M. Paul, Natalie Hauser, Jennifer L. Sloan, Andrea Gropman, Irini Manoli, Charles P. Venditti	15
18	Expanding the phenotypic profile of boys with 47, XXY: The impact of familial learning disabilities 2014 ·American Journal of Medical Genetics Part A ·Carole Samango‐Sprouse, Emily Stapleton, (unknown), Teresa Sadeghin, (unknown), Andrea Gropman	27
19	Brain magnetic resonance imaging findings in smith–lemli–opitz syndrome 2013 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Andrea Gropman, Forbes D. Porter, Eva H. Baker	35
20	Evidence Report: Genetic and metabolic testing on children with global developmental delay [RETIRED] 2011 ·Neurology ·David Michelson, Michael Shevell, Elliott H. Sherr, John B. Moeschler, Andrea Gropman, Stephen Ashwal	168

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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