Tatiana Foroud

73.6k total citations · 2 hit papers
405 papers, 20.1k citations indexed

About

Tatiana Foroud is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Tatiana Foroud has authored 405 papers receiving a total of 20.1k indexed citations (citations by other indexed papers that have themselves been cited), including 160 papers in Genetics, 154 papers in Molecular Biology and 76 papers in Neurology. Recurrent topics in Tatiana Foroud's work include Genetic Associations and Epidemiology (82 papers), Alcohol Consumption and Health Effects (55 papers) and Parkinson's Disease Mechanisms and Treatments (51 papers). Tatiana Foroud is often cited by papers focused on Genetic Associations and Epidemiology (82 papers), Alcohol Consumption and Health Effects (55 papers) and Parkinson's Disease Mechanisms and Treatments (51 papers). Tatiana Foroud collaborates with scholars based in United States, United Kingdom and Germany. Tatiana Foroud's co-authors include Howard J. Edenberg, Nathan Pankratz, John I. Nürnberger, Alison Goate, Danielle M. Dick, William C. Nichols, Marc A. Schuckit, Bernice Porjesz, Michael J. Econs and Victor Hesselbrock and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Tatiana Foroud

389 papers receiving 19.6k 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.

Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura

2001 1.3k citations Gallia G. Levy, William C. Nichols et al. Nature profile →
Structures of α-synuclein filaments from human brains with Lewy pathology

2022 262 citations Tatiana Foroud et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tatiana Foroud United States	76	7.1k	4.7k	4.5k	3.7k	3.5k	405	20.1k
Lindsay A. Farrer United States	71	7.4k 1.0×	3.1k 0.7×	4.4k 1.0×	1.7k 0.5×	7.2k 2.1×	425	23.6k
Margaret A. Pericak‐Vance United States	63	7.0k 1.0×	2.4k 0.5×	2.8k 0.6×	2.9k 0.8×	4.8k 1.4×	340	18.4k
Carlos A. Pardo United States	56	4.0k 0.6×	3.2k 0.7×	1.5k 0.3×	3.2k 0.9×	1.9k 0.6×	192	15.0k
Giovanni Coppola United States	71	7.9k 1.1×	6.2k 1.3×	1.6k 0.3×	2.7k 0.7×	3.4k 1.0×	274	18.7k
Guy A. Rouleau Canada	89	14.3k 2.0×	7.7k 1.7×	5.5k 1.2×	13.2k 3.6×	2.9k 0.8×	659	33.5k
Jeffery M. Vance United States	70	12.8k 1.8×	7.0k 1.5×	4.4k 1.0×	4.2k 1.1×	10.3k 3.0×	298	29.0k
Philip L. De Jager United States	73	8.3k 1.2×	1.7k 0.4×	3.4k 0.7×	1.6k 0.4×	4.5k 1.3×	392	19.4k
Howard J. Federoff United States	69	8.2k 1.2×	4.2k 0.9×	3.0k 0.7×	2.6k 0.7×	3.1k 0.9×	255	16.8k
Frank R. Sharp United States	87	12.3k 1.7×	7.3k 1.6×	1.5k 0.3×	4.1k 1.1×	3.9k 1.1×	376	27.7k
Richard H. Myers United States	76	9.3k 1.3×	8.4k 1.8×	3.0k 0.7×	5.9k 1.6×	2.3k 0.7×	239	19.7k

Countries citing papers authored by Tatiana Foroud

Since Specialization

Citations

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

Fields of papers citing papers by Tatiana Foroud

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tatiana Foroud

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Reitz, Christiane, Margaret A. Pericak‐Vance, Tatiana Foroud, & Richard Mayeux. (2023). A global view of the genetic basis of Alzheimer disease. Nature Reviews Neurology. 19(5). 261–277. 70 indexed citations

Johnson, Emma C., Jessica E. Salvatore, Dongbing Lai, et al.. (2023). The collaborative study on the genetics of alcoholism: Genetics. Genes Brain & Behavior. 22(5). e12856–e12856. 6 indexed citations

Edler, Michael, Samantha N. Smith, Tae‐Hwi Schwantes‐An, et al.. (2023). Implementing new technologies to enhance specimen quality and researcher value at the National Centralized Repository for Alzheimer’s Disease and Related Dementias. Alzheimer s & Dementia. 19(S14).

Reiter, Jill L., Andy Chen, Steven Chen, et al.. (2023). RNA alternative splicing impacts the risk for alcohol use disorder. Molecular Psychiatry. 28(7). 2922–2933. 4 indexed citations

Lai, Dongbing, Tae‐Hwi Schwantes‐An, Grace Chan, et al.. (2022). Gene-based polygenic risk scores analysis of alcohol use disorder in African Americans. Translational Psychiatry. 12(1). 266–266. 12 indexed citations

Ermel, Aaron, Thankam Thyvalikakath, Tatiana Foroud, Babar Khan, & Mythily Srinivasan. (2021). Can Salivary Innate Immune Molecules Provide Clue on Taste Dysfunction in COVID-19?. Frontiers in Microbiology. 12. 727430–727430. 2 indexed citations

Alcalay, Roy N., Pavlina Wolf, Ming Sum Ruby Chiang, et al.. (2020). Longitudinal Measurements of Glucocerebrosidase activity in Parkinson’s patients. Annals of Clinical and Translational Neurology. 7(10). 1816–1830. 25 indexed citations

Nudelman, Kelly, Jue Lin, Kathleen A. Lane, et al.. (2019). Telomere Shortening in the Alzheimer’s Disease Neuroimaging Initiative Cohort. PMC. 5 indexed citations

Edwards, Alexis C., Joseph D. Deak, Ian R. Gizer, et al.. (2018). Meta‐Analysis of Genetic Influences on Initial Alcohol Sensitivity. Alcoholism Clinical and Experimental Research. 42(12). 2349–2359. 19 indexed citations

10.

Leino, Daniel, Pascal J. Lafontant, Janice L. Farlow, et al.. (2018). Collagen COL22A1 maintains vascular stability and mutations in COL22A1 are potentially associated with intracranial aneurysms. PMC. 2 indexed citations

11.

Schneider, Bryan P., Fei Shen, Laura Gardner, et al.. (2016). Genome-Wide Association Study for Anthracycline-Induced Congestive Heart Failure. Clinical Cancer Research. 23(1). 43–51. 66 indexed citations

12.

Risacher, Shannon L., Sungeun Kim, Kwangsik Nho, et al.. (2015). APOE effect on Alzheimer's disease biomarkers in older adults with significant memory concern. eScholarship (California Digital Library). 4 indexed citations

13.

Olfson, Emily, Howard J. Edenberg, John I. Nürnberger, et al.. (2014). An ADH1B variant and peer drinking in progression to adolescent drinking milestones: Evidence of a gene-by-environment interaction. eScholarship (California Digital Library).

14.

Reitz, Christiane, Giuseppe Tosto, Badri N. Vardarajan, et al.. (2013). Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP). Translational Psychiatry. 3(5). e256–e256. 58 indexed citations

15.

Reitz, Christiane, Ekaterina Rogaeva, Tatiana Foroud, & Lindsay A. Farrer. (2011). Genetics and Genomics of Late‐Onset Alzheimer′s Disease and Its Endophenotypes. International Journal of Alzheimer s Disease. 2011(1). 284728–284728. 11 indexed citations

16.

Broderick, Joseph P., Robert D. Brown, Laura Sauerbeck, et al.. (2009). Greater Rupture Risk for Familial as Compared to Sporadic Unruptured Intracranial Aneurysms. Stroke. 40(6). 1952–1957. 134 indexed citations

17.

Edenberg, Howard J., Jianfeng Wang, Huijun Tian, et al.. (2008). A regulatory variation in OPRK1, the gene encoding the -opioid receptor, is associated with alcohol dependence. Human Molecular Genetics. 17(12). 1783–1789. 49 indexed citations

18.

Koller, Daniel L., Richard Snyder, Tonya Fishburn, et al.. (2005). Analysis of variation in expression of autosomal dominant osteopetrosis type 2: Searching for modifier genes. Bone. 37(5). 655–661. 27 indexed citations

19.

Levy, Gallia G., William C. Nichols, Eric C.‐Y. Lian, et al.. (2001). Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature. 413(6855). 488–494. 1254 indexed citations breakdown →

20.

Takács, István, Daphne Koller, Munro Peacock, et al.. (2000). Sib pair linkage and association studies between bone mineral density and the interleukin-6 gene locus. Bone. 27(1). 169–173. 28 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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