Author

Alan J. Lerner

University Hospitals Cleveland Medical Center

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 3

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:CITE-seq· 1 Research Focus:differential expression· 1 Assay:GWAS summary statistics· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Jonathan L. HainesiD· 3 shared Kristy L. S. MiskimeniD· 3 shared Margaret Ann Pericak‐VanceiD· 3 shared Reneé A. Laux· 3 shared Sarada L. Fuzzell· 3 shared Sherri D. Hochstetler· 3 shared William K. ScottiD· 3 shared Yeunjoo E. SongiD· 3 shared

Activity by Year

2022-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Jonathan L. HainesORCID

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3 papers

Recent·Most cited

Evidence for reduced somatic T-cell receptor sequence diversity profiles among Midwestern Amish in an aging cohort study

Lauren A. Cruz, Shiying Liu, Kristy L. S. Miskimen, Jessica N. Cooke Bailey, Tyler G. Kinzy, Yeunjoo E. Song, Reneé A. Laux, Penelope L. Miron, Paula K. Ogrocki, Alan J. Lerner, Audrey Lynn, Sarada L. Fuzzell, Sherri D. Hochstetler, Ioanna Konidari, Jacob L. McCauley, , Dana C. Crawford

The paper examines T-cell receptor sequence diversity and HLA alleles in Midwestern Amish participants to explore associations with Alzheimer's disease and cognitive status.

Annals of Human Genetics · Oct 18, 2026Peer-reviewedGenetic & Genomic Medicine

Heritability and rare variant contributions to Alzheimer disease in the Midwestern Amish

Yining Liu, Yeunjoo E. Song, Weihuan Wang, Audrey Lynn, Kristy L. S. Miskimen, Sarada L. Fuzzell, Sherri D. Hochstetler, Reneé A. Laux, Dawn Miller, Penelope L. Miron, Laura J. Caywood, Jason E. Clouse, Sharlene D. Herinton, Ping Wang, Alex V. Gulyayev, , Jonathan L. Haines

The paper estimates heritability and identifies genetic variants, including rare ones, associated with Alzheimer disease in the Amish population.

medRxiv · Sep 20, 2026 · PreprintGenetic & Genomic Medicine

Genetic variants in the SHISA6 gene are associated with delayed cognitive impairment in two family datasets

Jairo D. Ramos, Laura J. Caywood, Michael B. Prough, Jason E. Clouse, Sharlene D. Herington, Susan H. Slifer, M. Denise Fuzzell, Sarada L. Fuzzell, Sherri D. Hochstetler, Kristy L. S. Miskimen, Leighanne R. Main, Michael D. Osterman, Owen Laframboise, Andrew F. Zaman, Patrice L. Whitehead, , William K. Scott

The paper identifies three SNVs associated with delayed age at onset of cognitive impairment in Amish populations, with one replicated in an independent dataset and linked to the SHISA6 gene.

Alzheimer s & Dementia · May 1, 2022Peer-reviewedGenetic & Genomic Medicine