Marc S. Greenblatt

14.7k citations

64 papers · 7.8k indexed · 6 hit papers · h-index 25

Molecular Biology top 1%
Oncology top 0.5%
Genetics top 0.5%
Cancer Research top 0.5%
Pathology and Forensic Medicine top 0.5%

Co-authors: C C Harris W P Bennett Monica Hollstein Sean V. Tavtigian Johan T. den Dunnen Raymond Dalgleish Donna Maglott Anne‐Françoise Roux
Topics: Genomics and Rare Diseases (23 papers)Genetic factors in colorectal cancer (22 papers)Cancer Genomics and Diagnostics (18 papers)
Cited by: Cancer Research Oncology Genetics
Journals: Nucleic Acids Research Nature GeneticsSHILAP Revista de lepidopterología
Partner nations: United States Australia France

In The Last Decade

Marc S. Greenblatt

62 papers receiving 7.7k citations

Hit Papers

5 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 the p53 tumor suppressor gene: clues to cancer etiology and molecular pathogenesis.

1994 2.9k citations Marc S. Greenblatt et al. profile →
HGVS Recommendations for the Description of Sequence Variants: 2016 Update

2016 1.0k citations Johan T. den Dunnen, Marc S. Greenblatt et al. Human Mutation profile →
Database of p53 gene somatic mutations in human tumors and cell lines.

1994 727 citations Marc S. Greenblatt et al. profile →
Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results

2008 582 citations Sharon E. Plon, Diana Eccles et al. Human Mutation profile →
Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework

2019 310 citations Marc S. Greenblatt, Sean V. Tavtigian et al. profile →
Modeling the ACMG/AMP variant classification guidelines as a Bayesian classification framework

2018 279 citations Sean V. Tavtigian, Marc S. Greenblatt et al. Genetics in Medicine profile →

Peers

Countries citing papers authored by Marc S. Greenblatt

Since Specialization

Citations

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

Fields of papers citing papers by Marc S. Greenblatt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marc S. Greenblatt. 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 Marc S. Greenblatt. The network helps show where Marc S. Greenblatt may publish in the future.

Co-authorship network of co-authors of Marc S. Greenblatt

This figure shows the co-authorship network connecting the top 25 collaborators of Marc S. Greenblatt. A scholar is included among the top collaborators of Marc S. Greenblatt 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 Marc S. Greenblatt. Marc S. Greenblatt 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

#	Work	Indexed citations
1	Functional Characterization of a Genetic Variant in the 5′ UTR of APC 1B Promoter in a Familial Adenomatous Polyposis Family 2025 ·American Journal of Medical Genetics Part A ·(unknown),Deborah W. Neklason,Kathleen A. Clark,Bing Feng,(unknown),Thérèse M.F. Tuohy,(unknown),Wendy McKinnon,Marc S. Greenblatt,Sean V. Tavtigian	1
2	Phenotype Correlations With Pathogenic DNA Variants in the MUTYH Gene: A Review of Over 2000 Cases 2024 ·Human Mutation ·(unknown),John‐Paul Plazzer,Gabriel Capellá,Andrew Latchford,(unknown),Marc S. Greenblatt,Finlay Macrae	2
3	Assessment of the evidence yield for the calibrated PP3/BP4 computational recommendations 2024 ·Genetics in Medicine ·Sarah L. Stenton,Vikas Pejaver,Timothy Bergquist,Leslie G. Biesecker,Alicia B. Byrne,(unknown),Marc S. Greenblatt,Steven M. Harrison,Sean V. Tavtigian,Predrag Radivojac,Steven E. Brenner,Anne O’Donnell‐Luria,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	5
4	Improving transparency of computational tools for variant effect prediction 2024 ·Nature Genetics ·Rachel Karchin,Predrag Radivojac,Anne O’Donnell‐Luria,Marc S. Greenblatt,Michael Tolstorukov,Dmitriy Sonkin	6
5	Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndrome 2020 ·Genetics in Medicine ·Mark Drost,(unknown),(unknown),Scott D. Kathe,(unknown),Fabienne M.G.R. Calléja,José B.M. Zonneveld,Kenneth M. Boucher,(unknown),Bryony A. Thompson,Lene Juel Rasmussen,Marc S. Greenblatt,(unknown),Amanda B. Spurdle,Sean V. Tavtigian,Niels de Wind	16
6	Modeling the ACMG/AMP variant classification guidelines as a Bayesian classification frameworkbreakdown → 2018 ·Genetics in Medicine ·Sean V. Tavtigian,Marc S. Greenblatt,Steven M. Harrison,Robert L. Nussbaum,Snehit Prabhu,Kenneth M. Boucher,Leslie G. Biesecker	279
7	Multi-gene panel testing for hereditary cancer susceptibility in a rural Familial Cancer Program 2016 ·Familial Cancer ·(unknown),Wendy McKinnon,Marie Wood,Marc S. Greenblatt	11
8	Universal Versus Targeted Screening for Lynch Syndrome: Comparing Ascertainment and Costs Based on Clinical Experience 2016 ·Digestive Diseases and Sciences ·(unknown),(unknown),(unknown),Wendy McKinnon,Brandie Heald,Christopher Koliba,Marc S. Greenblatt	17
9	Therapeutic implications for ovarian cancer emerging from the Tumor Cancer Genome Atlas 2015 ·Translational Cancer Research ·Claire F. Verschraegen,Karen M. Lounsbury,Alan K. Howe,Marc S. Greenblatt	1
10	A Semantic Network for Modeling Biological Knowledge in Multiple Databases 2015 ·Communications of the IIMA ·(unknown),Xindong Wu,Marc S. Greenblatt	0
11	Colonic ganglioneuromatous polyposis and metastatic adenocarcinoma in the setting of Cowden syndrome: a case report and literature review 2011 ·Human Pathology ·(unknown),(unknown),Deborah Cook,Wendy McKinnon,Marc S. Greenblatt,Marcus Bosenberg	30
12	Locus-specific databases and recommendations to strengthen their contribution to the classification of variants in cancer susceptibility genes 2008 ·Human Mutation ·Marc S. Greenblatt,Lawrence C. Brody,William D. Foulkes,Maurizio Genuardi,Robert M.W. Hofstra,Magali Olivier,Sharon E. Plon,Rolf H. Sijmons,Olga M. Sinilnikova,Amanda B. Spurdle,(unknown)	30
13	Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test resultsbreakdown → 2008 ·Human Mutation ·Sharon E. Plon,Diana Eccles,Douglas F. Easton,William D. Foulkes,Maurizio Genuardi,Marc S. Greenblatt,Frans B.L. Hogervorst,Nicoline Hoogerbrugge,Amanda B. Spurdle,Sean V. Tavtigian,(unknown)	582
14	Assessing pathogenicity: overview of results from the IARC Unclassified Genetic Variants Working Group 2008 ·Human Mutation ·Sean V. Tavtigian,Marc S. Greenblatt,David E. Goldgar,Paolo Boffetta,(unknown)	60
15	Genetic evidence and integration of various data sources for classifying uncertain variants into a single model 2008 ·Human Mutation ·David E. Goldgar,Douglas F. Easton,Graham Byrnes,Amanda B. Spurdle,Edwin S. Iversen,Marc S. Greenblatt,(unknown)	125
16	Uncertain pathogenicity of MSH2 variants N127S and G322D challenges their classification 2008 ·International Journal of Cancer ·Saara Ollila,Denis Đermadi,Marc S. Greenblatt,Minna Nyström	7
17	A structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases 2007 ·Human Mutation ·Richard G.H. Cotton,Arleen D. Auerbach,A. F. Brown,Paola Carrera,John Christodoulou,Mireille Claustres,John G. Compton,D W Cox,Elfride De Baere,Johan T. den Dunnen,Marc S. Greenblatt,Makoto Fujiwara,Pascale Hilbert,(unknown),Heikki Lehväslaiho,Daniel W. Nebert,Ishwar C. Verma,Mauno Vihinen	9
18	Pathogenicity of MSH2 Missense Mutations Is Typically Associated With Impaired Repair Capability of the Mutated Protein 2006 ·Gastroenterology ·Saara Ollila,Laura Sarantaus,Reetta Kariola,Philip A. Chan,Heather Hampel,Elke Holinski‐Feder,Finlay Macrae,Maija R.J. Kohonen‐Corish,Anne‐Marie Gerdes,Païvi Peltomäki,Elisabeth Mangold,Albert de la Chapelle,Marc S. Greenblatt,Minna Nyström	54
19	An intelligent digital library system for biologists 2004 ·(unknown),Xindong Wu,Marc S. Greenblatt	1
20	Does Aflatoxin B₁Play a Role in the Etiology of Hepatocellular Carcinoma in the United States? 1999 ·Nutrition and Cancer ·Ashraful Hoque,Yehuda Z. Patt,Boris Yoffe,John D. Groopman,Marc S. Greenblatt,Yujing Zhang,Regina M. Santella	16

About Marc S. Greenblatt

Marc S. Greenblatt is a scholar working on Cancer Research, Pathology and Forensic Medicine and Genetics, having authored 64 papers that have together received 7.8k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (23 papers), Genetic factors in colorectal cancer (22 papers) and Cancer Genomics and Diagnostics (18 papers). The work is most often cited by research in Cancer Research (2.0k citations), Oncology (3.3k citations) and Genetics (2.2k citations). Marc S. Greenblatt has collaborated with scholars based in United States, Australia and France. Frequent co-authors include C C Harris, W P Bennett, Monica Hollstein, Sean V. Tavtigian, Johan T. den Dunnen, Raymond Dalgleish, Donna Maglott, Anne‐Françoise Roux, Jean McGowan‐Jordan and Stylianos E. Antonarakis. Their work appears in journals such as Nucleic Acids Research, Nature Genetics and SHILAP Revista de lepidopterología.

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