Jhih-Rong Lin

Albert Einstein College of Medicine — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

7h-index280citations25works1.32yr avg
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Research Topics

Genetic Associations and Epidemiology(5), Bioinformatics and Genomic Networks(5), Genetics and Neurodevelopmental Disorders(5), Machine Learning in Bioinformatics(5), Congenital heart defects research(4)

Publications25 total

Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome
2026Open Access
The Somatic Aneuploidy Landscape of Adult Glia Reveals 16p as a Hotspot and Differentiates Mosaicism in Normal Glia from Chromosomal Instability in Glioblastoma
2025Open Access
Chromosomal Aneuploidy in Normal, Non-Neuronal Brain Nuclei of Glioblastoma Patients is Not a Cancer Driver
2025Open Access
Ultrarare Variants in DNA Damage Repair Genes in Pediatric Acute-Onset Neuropsychiatric Syndrome or Acute Behavioral Regression in Neurodevelopmental Disorders
Developmental Neuroscience·2024· 6 citedOpen Access
Author Correction: Rare genetic coding variants associated with human longevity and protection against age-related diseases
Nature Aging·2024Open Access
Polygenic prediction of human longevity on the supposition of pervasive pleiotropy
Scientific Reports·2024· 2 citedOpen Access
Rare genetic coding variants associated with age-related episodic memory decline implicate distinct memory pathologies in the hippocampus
2024· 1 citedOpen Access
Polygenic prediction of human longevity on the supposition of pervasive pleiotropy
2023Open Access
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS
npj Genomic Medicine·2023· 11 citedOpen Access
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia
Molecular Psychiatry·2023· 4 citedOpen Access
Mitochondrial DNA Copy Number Is Associated With Treatment Response and Cognitive Function in Euthymic Bipolar Patients Receiving Valproate.
PubMed·2022· 5 citedOpen Access
Mitochondrial DNA Copy Number Is Associated With Treatment Response and Cognitive Function in Euthymic Bipolar Patients Receiving Valproate
The International Journal of Neuropsychopharmacology·2022· 9 citedOpen Access
Genomic expansion of Aldh1a1 protects beavers against high metabolic aldehydes from lipid oxidation
Cell Reports·2021· 16 citedOpen Access
Rare genetic coding variants associated with human longevity and protection against age-related diseases
Nature Aging·2021· 47 citedOpen Access
Deep Post-GWAS Analysis Identifies Potential Risk Genes and Causal Variants for Alzheimer’s Disease, Providing New Insights Into Its Disease Mechanisms
Research Square (Research Square)·2020Open Access
The genome of North American beaver provides insights into the mechanisms of its longevity and cancer resistance
2020· 1 citedOpen Access
Deep Post-GWAS Analysis Identifies Potential Risk Genes and Causal Variants for Alzheimer’s Disease, Providing New Insights Into Its Disease Mechanisms
Research Square (Research Square)·2020· 1 citedOpen Access
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
Molecular Psychiatry·2020· 132 citedOpen Access
Additional file 2: of Transcriptomic dynamics of breast cancer progression in the MMTV-PyMT mouse model
Figshare·2017Open Access
Abstract 175: Transcriptomic and epigenetic dynamics of breast cancer progression in the MMTV-PyMT mouse model
Cancer Research·2016
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Frequent Co-authors

Zhengdong D. Zhang(13), Joydeep Mitra(9), Nha Nguyen(9), Quanwei Zhang(8), M. Reza Jabalameli(8), Jan Vijg(7), Bernice E. Morrow(5), Zhengdong Zhang(5), Sofiya Milman(5), Nir Barzilai(5), Jacob Vorstman(4), Tina Gao(4), Gil Atzmon(4), Vera Gorbunova(4), Jianjun Hu(4), Cristina Montagna(4), Donna M. McDonald‐McGinn(3), Raquel E. Gur(3), Ann Swillen(3), Carrie E. Bearden(3)