John M. Greally

Albert Einstein College of Medicine — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

69h-index17.2kcitations423works2.92yr avg
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Research Topics

Epigenetics and DNA Methylation(193), Cancer-related gene regulation(57), RNA modifications and cancer(51), Acute Myeloid Leukemia Research(49), Genomics and Chromatin Dynamics(46)

Publications422 total

Integrating multi-omic QTLs and predictive models reveals regulatory architectures at immune related GWAS loci in CD4+ T cells
2026Open Access
Egr1 is a sex-dependent regulator of neuronal chromatin, structural plasticity, and behaviour
Nature Communications·2025· 1 citedOpen Access
Individuals with intellectual disability have an increased burden of <i>de novo</i> variants in <i>cis</i> -regulatory elements of glutamatergic neurons
2025Open Access
Editorial Expression of Concern: Bcl-6 mediates the germinal center B cell phenotype and lymphomagenesis through transcriptional repression of the DNA-damage sensor ATR
Nature Immunology·2025Open Access
MYH11 rare variant augments aortic growth and induces cardiac hypertrophy and heart failure with pressure overload
PLoS Genetics·2025Open Access
Identifying the Genetic Ancestry of the Pediatric Obesity‐Related Asthma Variant (rs6494395) at <i>Rps27l</i>
Pediatric Pulmonology·2025Open Access
Genetic disease risks of under-represented founder populations in New York City
PLoS Genetics·2025· 1 citedOpen Access
Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption
Nature Genetics·2025· 27 citedOpen Access
Investigating the Impact of Screen-Sharing Visual Aids during Genomic Results Disclosure via Telehealth in Diverse Families in the TeleKidSeq Pilot Study
Public Health Genomics·2025· 1 citedOpen Access
Patient and providers’ perspectives on using the GUÍA digital tool to enhance genomic results disclosure
Genetics in Medicine Open·2025Open Access
P223: Discovery of rare disease variants specific to populations using genomic data from diverse populations in All of Us
Genetics in Medicine Open·2025Open Access
Employing effective recruitment and retention strategies to engage a diverse pediatric population in genomics research
The American Journal of Human Genetics·2024· 2 citedOpen Access
Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption
2024· 3 cited
Clinical Utility of Polygenic Risk Scores for Embryo Selection: A Points to Consider Statement of the American College of Medical Genetics and Genomics (ACMG)
Obstetrical & Gynecological Survey·2024
Genetic disease risks of under-represented founder populations in New York City
2024· 3 citedOpen Access
Prenatal vitamin D deficiency exposure leads to long-term changes in immune cell proportions
Scientific Reports·2024· 5 citedOpen Access
Single-cell analysis identifies distinct CD4+ T cells associated with the pathobiology of pediatric obesity-related asthma
2024· 4 citedOpen Access
<i>MYH11</i> rare variant augments aortic growth and induces cardiac hypertrophy and heart failure with pressure overload
2024· 3 citedOpen Access
Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual population
Human Genetics and Genomics Advances·2024Open Access
Response to Widen et al
Genetics in Medicine·2024Open Access
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Frequent Co-authors

Masako Suzuki(15), Ari Melnick(10), Amit Verma(10), Melissa Fazzari(8), Tushar D. Bhagat(7), María E. Figueroa(6), Reid F. Thompson(6), Yiting Yu(6), Jacob L. Glass(4), Ulrich Steidl(4), Yushan Li(3), Lucy Skrabanek(3), Cristina Montagna(3), Eli Hatchwell(3), Li Zhou(3), Carolina Schinke(3), Nir Barzilai(3), Sanchari Bhattacharyya(3), Yongkai Mo(3), Kyung‐Min Noh(2)