Allison E. Ashley‐Koch

30.5k total citations
210 papers, 8.3k citations indexed

About

Allison E. Ashley‐Koch is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Allison E. Ashley‐Koch has authored 210 papers receiving a total of 8.3k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Molecular Biology, 48 papers in Genetics and 40 papers in Genetics. Recurrent topics in Allison E. Ashley‐Koch's work include Hemoglobinopathies and Related Disorders (44 papers), Autism Spectrum Disorder Research (23 papers) and Genetics and Neurodevelopmental Disorders (23 papers). Allison E. Ashley‐Koch is often cited by papers focused on Hemoglobinopathies and Related Disorders (44 papers), Autism Spectrum Disorder Research (23 papers) and Genetics and Neurodevelopmental Disorders (23 papers). Allison E. Ashley‐Koch collaborates with scholars based in United States, Canada and Singapore. Allison E. Ashley‐Koch's co-authors include Melanie E. Garrett, Marilyn J. Telen, Quanhe Yang, Richard S. Olney, Michael L. Cuccaro, Michael A. Hauser, Jude Jonassaint, Laura M. De Castro, Margaret A. Pericak‐Vance and Jeffery M. Vance and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Allison E. Ashley‐Koch

196 papers receiving 8.1k citations

Peers

Countries citing papers authored by Allison E. Ashley‐Koch

Since Specialization

Citations

This map shows the geographic impact of Allison E. Ashley‐Koch's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Allison E. Ashley‐Koch with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Allison E. Ashley‐Koch more than expected).

Fields of papers citing papers by Allison E. Ashley‐Koch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Allison E. Ashley‐Koch. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Allison E. Ashley‐Koch. The network helps show where Allison E. Ashley‐Koch may publish in the future.

Co-authorship network of co-authors of Allison E. Ashley‐Koch

This figure shows the co-authorship network connecting the top 25 collaborators of Allison E. Ashley‐Koch. A scholar is included among the top collaborators of Allison E. Ashley‐Koch based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Allison E. Ashley‐Koch. Allison E. Ashley‐Koch is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Accelerated Epigenetic Aging and Prospective Morbidity and Mortality Among U.S. Veterans 2025 ·The Journals of Gerontology Series A ·Kyle J. Bourassa, (unknown), Sandra Woolson, Paul A. Dennis, Melanie E. Garrett, Lauren P. Hair, Michelle F. Dennis, Karen Sugden, Benjamin Williams, Renate Houts, Patrick S. Calhoun, Jennifer C. Naylor, Allison E. Ashley‐Koch, Jean C. Beckham, Avshalom Caspi, Gregory A. Taylor, Katherine S. Hall, Terrie E. Moffitt, Nathan A. Kimbrel, (unknown)	3
2	Comparative mapping of single‐cell transcriptomic landscapes in neurodegenerative diseases 2025 ·Alzheimer s & Dementia ·E. Keats Shwab, (unknown), (unknown), (unknown), Melanie E. Garrett, Geidy E. Serrano, Thomas G. Beach, Gregory E. Crawford, Allison E. Ashley‐Koch, Ornit Chiba‐Falek	1
3	Traumatic Brain Injury and Accelerated Epigenetic Aging Among Post-9/11 Veterans 2025 ·Journal of Head Trauma Rehabilitation ·Kyle J. Bourassa, Sarah L. Martindale, Melanie E. Garrett, Allison E. Ashley‐Koch, Jean C. Beckham, Nathan A. Kimbrel, Jared A. Rowland	0
4	Demographic characteristics and epigenetic biological aging among post-9/11 veterans: Associations of DunedinPACE with sex, race, and age 2024 ·Psychiatry Research ·Kyle J. Bourassa, Tate F. Halverson, Melanie E. Garrett, Lauren P. Hair, Michelle F. Dennis, Allison E. Ashley‐Koch, Jean C. Beckham, Nathan A. Kimbrel	4
5	Single‐cell transcriptomic landscapes of neurodegenerative diseases: towards mapping shared and distinct mechanisms 2024 ·Alzheimer s & Dementia ·E. Keats Shwab, (unknown), (unknown), Melanie E. Garrett, Gregory E. Crawford, Allison E. Ashley‐Koch, Ornit Chiba‐Falek	0
6	Social connection and suicidal thoughts and behaviors in the Million Veteran Program cohort 2024 ·Journal of Psychiatric Research ·Kyle J. Bourassa, Paul A. Dennis, (unknown), Xuejun Qin, David A. Sbarra, Elizabeth R. Hauser, Allison E. Ashley‐Koch, (unknown), Jean C. Beckham, Nathan A. Kimbrel	0
7	Acute perioperative alterations in metabolism: A pilot study using mass spectrometry–based metabolomics 2024 ·Surgery ·Keri A. Seymour, (unknown), Allison E. Ashley‐Koch, Michael J. Muehlbauer, Olga Ilkayeva, Tabitha George, (unknown), (unknown), Satoru Ito, Sandhya Lagoo‐Deenadayalan, Jennifer K. Plichta, J. Todd Purves, Julie K. Thacker, (unknown), Allan D. Kirk, (unknown), James R. Bain	0
8	Large epigenome-wide association study identifies multiple novel differentially methylated CpG sites associated with suicidal thoughts and behaviors in veterans 2023 ·Frontiers in Psychiatry ·Nathan A. Kimbrel, Melanie E. Garrett, (unknown), (unknown), Michelle F. Dennis, Lauren P. Hair, Michael A. Hauser, (unknown), Allison E. Ashley‐Koch, Jean C. Beckham	7
9	Lysyl oxidase-like 1-antisense 1 (LOXL1-AS1) lncRNA differentially regulates gene and protein expression, signaling and morphology of human ocular cells 2023 ·Human Molecular Genetics ·H Schmitt, (unknown), Kristin Perkumas, (unknown), María F. Suárez, Michael L. De Ieso, (unknown), William M. Johnson, María Gomez‐Caraballo, Allison E. Ashley‐Koch, Michael A. Hauser, W. Daniel Stamer	6
10	Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program 2020 ·Transfusion ·Carla Luana Dinardo, Théo Gremen Mimary de Oliveira, Shannon Kelly, Allison E. Ashley‐Koch, Marilyn J. Telen, (unknown), (unknown), Karla Melo, (unknown), Marsha M. Wheeler, Jill M. Johnsen, Deborah A. Nickerson, Deepti Jain, Brian Custer, Alexandre C. Pereira, Éster Cerdeira Sabino, (unknown)	9
11	Development of Common Data Elements for Use in Chiari Malformation Type I Clinical Research: An NIH/NINDS Project 2019 ·Neurosurgery ·Mark G. Luciano, Ulrich Batzdorf, Roger W. Kula, Brandon G. Rocque, Cormac O. Maher, John D. Heiss, Bryn A. Martin, Paolo A. Bolognese, Allison E. Ashley‐Koch, David D. Limbrick, (unknown), (unknown), Joanne Odenkirchen, Joy Esterlitz, (unknown), (unknown), Robin Feldman, (unknown), (unknown)	19
12	Systematic Functional Testing of Rare Variants: Contributions of CFI to Age-Related Macular Degeneration 2017 ·Investigative Ophthalmology & Visual Science ·Perciliz L. Tan, Melanie E. Garrett, Jason R. Willer, Peter A. Campochiaro, Betsy Campochiaro, Donald J. Zack, Allison E. Ashley‐Koch, Nicholas Katsanis	14
13	Transcriptome analysis of adult and fetal trabecular meshwork, cornea, and ciliary body tissues by RNA sequencing 2016 ·Experimental Eye Research ·Megan Ulmer Carnes, R. Rand Allingham, Allison E. Ashley‐Koch, Michael A. Hauser	36
14	Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics 2014 ·BMC Medical Genomics ·Christina A. Markunas, Eric F. Lock, Karen Soldano, Heidi Cope, Chien‐Kuang Cornelia Ding, David S. Enterline, Gerald A. Grant, Herbert E. Fuchs, Allison E. Ashley‐Koch, Simon G. Gregory	23
15	Gene-centric association study of acute chest syndrome and painful crisis in sickle cell disease patients 2013 ·Blood ·Geneviève Galarneau, Sean Coady, Melanie E. Garrett, Neal Jeffries, Mona Puggal, Dina N. Paltoo, Karen Soldano, Antonio Guasch, Allison E. Ashley‐Koch, Marilyn J. Telen, Abdullah Kutlar, Guillaume Lettre, George Papanicolaou	25
16	The role of SIX6 in primary open-angle glaucoma 2013 ·Investigative Ophthalmology & Visual Science ·Michael A. Hauser, Megan Ulmer, Yangfan Liu, Erica E. Davis, Nicholas Katsanis, Yutao Liu, Louis R. Pasquale, Janey L. Wiggs, Allison E. Ashley‐Koch, R. Rand Allingham	1
17	Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism 2005 ·The American Journal of Human Genetics ·(unknown), Patrice L. Whitehead, Marisa M. Menold, Eden R. Martin, Allison E. Ashley‐Koch, Hao Mei, Marylyn D. Ritchie, G. R. DeLong, Ruth K. Abramson, H Wright, Michael L. Cuccaro, John P. Hussman, John R. Gilbert, Margaret A Pericak‐Vance	269
18	Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder 2001 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Yujun Shao, Kimberly L. Raiford, Chantelle M. Wolpert, Allison E. Ashley‐Koch, Michael L. Cuccaro, John R. Gilbert, M. A. Pericak‐Vance	1
19	Screening for MECP2 mutations in females with autistic disorder 2001 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Allison E. Ashley‐Koch, (unknown), Chantelle M. Wolpert, Michael L. Cuccaro, (unknown), Jeffery M. Vance, Margaret A. Pericak‐Vance	2
20	Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population 1996 ·American Journal of Medical Genetics ·Kellen L. Meadows, Dorothy Pettay, James L. Newman, (unknown), Allison E. Ashley‐Koch, Stephanie L. Sherman	3

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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