Marc Greenblatt

Marc Greenblatt

University of Vermont

H-index: 39

North America-United States

About Marc Greenblatt

Marc Greenblatt, With an exceptional h-index of 39 and a recent h-index of 21 (since 2020), a distinguished researcher at University of Vermont, specializes in the field of Cancer Genetics.

His recent articles reflect a diverse array of research interests and contributions to the field:

Gene-specific ACMG/AMP classification criteria for germline APC variants: recommendations from the ClinGen InSiGHT hereditary colorectal cancer/polyposis variant curation …

Assessment of the evidence yield for the calibrated PP3/BP4 computational recommendations

CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods

Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the …

P364: Exploring the effects of a point mutation in the 5’UTR of APC found in a family with colon cancer

Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup

Eliminating barriers to uptake of germline genetic testing for patients with advanced cancer: The GTAC study.

Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria

Marc Greenblatt Information

University

Position

Associate Professor of Medicine

Citations(all)

15838

Citations(since 2020)

4268

Cited By

12978

hIndex(all)

39

hIndex(since 2020)

21

i10Index(all)

71

i10Index(since 2020)

45

Email

University Profile Page

Google Scholar

Marc Greenblatt Skills & Research Interests

Cancer Genetics

Top articles of Marc Greenblatt

Gene-specific ACMG/AMP classification criteria for germline APC variants: recommendations from the ClinGen InSiGHT hereditary colorectal cancer/polyposis variant curation …

Genetics in Medicine

2024/2/1

Assessment of the evidence yield for the calibrated PP3/BP4 computational recommendations

medRxiv

2024

Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the …

EClinicalMedicine

2023/4/1

P364: Exploring the effects of a point mutation in the 5’UTR of APC found in a family with colon cancer

Genetics in Medicine Open

2023/1/1

Marc Greenblatt
Marc Greenblatt

H-Index: 22

Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup

The American Journal of Human Genetics

2023/7/6

Eliminating barriers to uptake of germline genetic testing for patients with advanced cancer: The GTAC study.

2023/6/1

Sarah A Nowak
Sarah A Nowak

H-Index: 9

Marc Greenblatt
Marc Greenblatt

H-Index: 22

Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria

The American Journal of Human Genetics

2022/12/1

Evidence-based calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for clinical use of PP3/BP4 criteria

bioRxiv

2022/3/19

Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

European Journal of Cancer

2021/5/1

Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

Genetics in Medicine

2021/4

Analysis in the Prospective Lynch Syndrome Database identifies sarcoma as part of the Lynch syndrome tumor spectrum

International Journal of Cancer

2021/1/15

No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome …

Journal of clinical medicine

2021/6/28

Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework

Genome medicine

2020/12

Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database (Genetics in …

Genetics in Medicine

2020/9/1

Curated multiple sequence alignment for the Adenomatous Polyposis Coli (APC) gene and accuracy of in silico pathogenicity predictions

Plos one

2020/8/4

Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndrome

Genetics in Medicine

2020/5

Cancer risks by gene, age, and gender in 6350 carriers ofpathogenic mismatch repair variants: findings from the Prospective Lynch SyndromeDatabase

Genetics in Medicine

2020

See List of Professors in Marc Greenblatt University(University of Vermont)