Michael N. Cantor

Internal Medicine

462 1st Ave Ste 2C
New York, NY 10016

Last Updated: 09/26/2026

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Found 35 publications

Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.

Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.

Journal: Nature

Published: January 08, 2025

Rare coding variants in CHRNB3 associate with reduced daily cigarette smoking across ancestries.

Rare coding variants in CHRNB3 associate with reduced daily cigarette smoking across ancestries.

Journal: Nature communications

Published: December 06, 2024

Pharmacologic and Genetic Downregulation of Proprotein Convertase Subtilisin/Kexin Type 9 and Survival From Sepsis.

Pharmacologic and Genetic Downregulation of Proprotein Convertase Subtilisin/Kexin Type 9 and Survival From Sepsis.

Journal: Critical care explorations

Published: November 13, 2023

NOTCH3 p.Arg1231Cys is markedly enriched in South Asians and associated with stroke.

NOTCH3 p.Arg1231Cys is markedly enriched in South Asians and associated with stroke.

Journal: Nature communications

Published: November 09, 2023

Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.

Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.

Journal: Nature

Published: February 22, 2023

Rare coding variants in CHRNB2 reduce the likelihood of smoking.

Rare coding variants in CHRNB2 reduce the likelihood of smoking.

Journal: Nature genetics

Published: November 10, 2022

The effect of tablet computer-based telemonitoring added to an established telephone disease management program on heart failure hospitalizations: The Specialized Primary and Networked Care in Heart Failure (SPAN-CHF) III Randomized Controlled Trial.

The effect of tablet computer-based telemonitoring added to an established telephone disease management program on heart failure hospitalizations: The Specialized Primary and Networked Care in Heart Failure (SPAN-CHF) III Randomized Controlled Trial.

Journal: American heart journal

Published: September 16, 2022

Germline Mutations in CIDEB and Protection against Liver Disease.

Germline Mutations in CIDEB and Protection against Liver Disease.

Journal: The New England journal of medicine

Published: August 08, 2022

Genetic risk factors for COVID-19 and influenza are largely distinct.

Genetic risk factors for COVID-19 and influenza are largely distinct.

Journal: Nature genetics

Published: July 12, 2022

Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis.

Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis.

Journal: Nature genetics

Published: February 08, 2022

Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes.

Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes.

Journal: Nature communications

Published: February 08, 2022

Common and rare variant associations with clonal haematopoiesis phenotypes.

Common and rare variant associations with clonal haematopoiesis phenotypes.

Journal: Nature

Published: December 23, 2021

Showing 1-12 of 35

Last Updated: 09/26/2026