Jaeyoon Chung, PhD
Research Assistant Professor
Boston University School of Medicine
Dept of Medicine
Biomedical Genetics

PhD, Boston University
MA, Korea University

Jaeyoon Chung, PhD is a Research Assistant Professor of Biomedical Genetics at Boston University School of Medicine.

Sequencing Annotation and Functional Analysis in Risk of Intracerebral Hemorrhage
12/01/2018 - 11/30/2022 (Subcontract PI)
Massachusetts General Hospital NIH NINDS


Yr Title Project-Sub Proj Pubs

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.

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  1. Jun GR, You Y, Zhu C, Meng G, Chung J, Panitch R, Hu J, Xia W, Bennett DA, Foroud TM, Wang LS, Haines JL, Mayeux R, Pericak-Vance MA, Schellenberg GD, Au R, Lunetta KL, Ikezu T, Stein TD, Farrer LA. Protein phosphatase 2A and complement component 4 are linked to the protective effect of APOE ?2 for Alzheimer's disease. Alzheimers Dement. 2022 Feb 09.View Related Profiles. PMID: 35142023
  2. Panitch R, Hu J, Chung J, Zhu C, Meng G, Xia W, Bennett DA, Lunetta KL, Ikezu T, Au R, Stein TD, Farrer LA, Jun GR. Integrative brain transcriptome analysis links complement component 4 and HSPA2 to the APOE e2 protective effect in Alzheimer disease. Mol Psychiatry. 2021 10; 26(10):6054-6064.View Related Profiles. PMID: 34480088; PMCID: PMC8758485; DOI: 10.1038/s41380-021-01266-z;
  3. Chung J, Hamilton G, Kim M, Marini S, Montgomery B, Henry J, Cho AE, Brown DL, Worrall BB, Meschia JF, Silliman SL, Selim M, Tirschwell DL, Kidwell CS, Kissela B, Greenberg SM, Viswanathan A, Goldstein JN, Langefeld CD, Rannikmae K, Sudlow CL, Samarasekera N, Rodrigues M, Al-Shahi Salman R, Prendergast JGD, Harris SE, Deary I, Woo D, Rosand J, Van Agtmael T, Anderson CD. Rare Missense Functional Variants at COL4A1 and COL4A2 in Sporadic Intracerebral Hemorrhage. Neurology. 2021 May 24. PMID: 34031201; PMCID: PMC8302151; DOI: 10.1212/WNL.0000000000012227;
  4. Loporchio DF, Tam EK, Cho J, Chung J, Jun GR, Xia W, Fiorello MG, Siegel NH, Ness S, Stein TD, Subramanian ML. Cytokine Levels in Human Vitreous in Proliferative Diabetic Retinopathy. Cells. 2021 04 30; 10(5).View Related Profiles. PMID: 33946446; PMCID: PMC8147162; DOI: 10.3390/cells10051069;
  5. Subramanian ML, Vig V, Chung J, Fiorello MG, Xia W, Zetterberg H, Blennow K, Zetterberg M, Shareef F, Siegel NH, Ness S, Jun GR, Stein TD. Neurofilament light chain in the vitreous humor of the eye. Alzheimers Res Ther. 2020 09 17; 12(1):111.View Related Profiles. PMID: 32943089; PMCID: PMC7500015; DOI: 10.1186/s13195-020-00677-4;
  6. Marini S, Georgakis MK, Chung J, Henry JQA, Dichgans M, Rosand J, Malik R, Anderson CD. Genetic overlap and causal inferences between kidney function and cerebrovascular disease. Neurology. 2020 06 16; 94(24):e2581-e2591. PMID: 32439819; PMCID: PMC7455337; DOI: 10.1212/WNL.0000000000009642;
  7. Falcone GJ, Kirsch E, Acosta JN, Noche RB, Leasure A, Marini S, Chung J, Selim M, Meschia JF, Brown DL, Worrall BB, Tirschwell DL, Jagiella JM, Schmidt H, Jimenez-Conde J, Fernandez-Cadenas I, Lindgren A, Slowik A, Gill D, Holmes M, Phuah CL, Petersen NH, Matouk Md CN, Gunel M, Sansing L, Bennett D, Chen Z, Sun LL, Clarke R, Walters RG, Gill TM, Biffi A, Kathiresan S, Langefeld CD, Woo D, Rosand J, Sheth KN, Anderson CD. Genetically Elevated LDL Associates with Lower Risk of Intracerebral Hemorrhage. Ann Neurol. 2020 07; 88(1):56-66. PMID: 32277781; PMCID: PMC7523882; DOI: 10.1002/ana.25740;
  8. Traylor M, Amin Al Olama A, Lyytikäinen LP, Marini S, Chung J, Malik R, Dichgans M, Kähönen M, Lehtimäki T, Anderson CD, Raitakari OT, Markus HS. Influence of Genetic Variation in PDE3A on Endothelial Function and Stroke. Hypertension. 2020 02; 75(2):365-371. PMID: 31865795; PMCID: PMC7055937; DOI: 10.1161/HYPERTENSIONAHA.119.13513;
  9. Chung J, Marini S, Pera J, Norrving B, Jimenez-Conde J, Roquer J, Fernandez-Cadenas I, Tirschwell DL, Selim M, Brown DL, Silliman SL, Worrall BB, Meschia JF, Demel S, Greenberg SM, Slowik A, Lindgren A, Schmidt R, Traylor M, Sargurupremraj M, Tiedt S, Malik R, Debette S, Dichgans M, Langefeld CD, Woo D, Rosand J, Anderson CD. Genome-wide association study of cerebral small vessel disease reveals established and novel loci. Brain. 2019 10 01; 142(10):3176-3189. PMID: 31430377; PMCID: PMC6763741; DOI: 10.1093/brain/awz233;
  10. Ma Y, Jun GR, Zhang X, Chung J, Naj AC, Chen Y, Bellenguez C, Hamilton-Nelson K, Martin ER, Kunkle BW, Bis JC, Debette S, DeStefano AL, Fornage M, Nicolas G, van Duijn C, Bennett DA, De Jager PL, Mayeux R, Haines JL, Pericak-Vance MA, Seshadri S, Lambert JC, Schellenberg GD, Lunetta KL, Farrer LA. Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype. JAMA Neurol. 2019 Sep 01; 76(9):1099-1108.View Related Profiles. PMID: 31180460; PMCID: PMC6563544; DOI: 10.1001/jamaneurol.2019.1456;
Showing 10 of 34 results. Show More

This graph shows the total number of publications by year, by first, middle/unknown, or last author.

Bar chart showing 34 publications over 14 distinct years, with a maximum of 8 publications in 2019


In addition to these self-described keywords below, a list of MeSH based concepts is available here.

Alzheimer disease
Statistical genetics
translational medicine
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