Amy Crunk

787 total citations
10 papers, 131 citations indexed

About

Amy Crunk is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Amy Crunk has authored 10 papers receiving a total of 131 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Neurology and 4 papers in Genetics. Recurrent topics in Amy Crunk's work include Neurological diseases and metabolism (4 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Nuclear Receptors and Signaling (2 papers). Amy Crunk is often cited by papers focused on Neurological diseases and metabolism (4 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Nuclear Receptors and Signaling (2 papers). Amy Crunk collaborates with scholars based in United States, United Kingdom and Qatar. Amy Crunk's co-authors include Lynne L. McFarland, Jonathan L. Haines, Bassel Abou‐Khalil, Peter Hedera, Jonathan L. Haines, James S. Sutcliffe, Charles E. Jackson, William K. Scott, P. C. Gaskell and Jacob L. McCauley and has published in prestigious journals such as Epilepsia, Neurobiology of Aging and Human Genetics.

In The Last Decade

Amy Crunk

8 papers receiving 130 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Amy Crunk United States	6	59	58	31	24	23	10	131
Laura L. Klitten Denmark	8	83 1.4×	108 1.9×	33 1.1×	6 0.3×	23 1.0×	10	209
Karit Reinson Estonia	8	67 1.1×	122 2.1×	23 0.7×	16 0.7×	15 0.7×	14	198
Mitja Kurki Finland	5	30 0.5×	76 1.3×	85 2.7×	23 1.0×	23 1.0×	6	165
Tara Skelly United States	7	57 1.0×	123 2.1×	25 0.8×	26 1.1×	51 2.2×	9	231
Linn Öijerstedt Sweden	5	26 0.4×	42 0.7×	45 1.5×	53 2.2×	14 0.6×	14	124
Manuela Casarano Italy	10	35 0.6×	74 1.3×	34 1.1×	14 0.6×	24 1.0×	15	206
Ashley P.L. Marsh Australia	6	44 0.7×	65 1.1×	23 0.7×	6 0.3×	27 1.2×	9	150
Suad Alyamani Saudi Arabia	4	22 0.4×	67 1.2×	13 0.4×	10 0.4×	23 1.0×	8	118
Ya-Hui Lin United Kingdom	6	46 0.8×	159 2.7×	20 0.6×	26 1.1×	29 1.3×	10	216

Countries citing papers authored by Amy Crunk

Since Specialization

Citations

This map shows the geographic impact of Amy Crunk'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 Amy Crunk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amy Crunk more than expected).

Fields of papers citing papers by Amy Crunk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amy Crunk. 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 Amy Crunk. The network helps show where Amy Crunk may publish in the future.

Co-authorship network of co-authors of Amy Crunk

This figure shows the co-authorship network connecting the top 25 collaborators of Amy Crunk. A scholar is included among the top collaborators of Amy Crunk 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 Amy Crunk. Amy Crunk is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

Mullegama, Sureni V., Amber Begtrup, Amy Crunk, et al.. (2025). A proposed role for CDO1 in CNS development: Three children with rare missense variants and a neurological phenotype. Human Genetics and Genomics Advances. 6(2). 100417–100417.

Aleem, Alice Abdel, et al.. (2023). Cohen syndrome and early-onset epileptic encephalopathy in male triplets: two disease-causing mutations in VPS13B and NAPB. Neurogenetics. 24(2). 103–112. 4 indexed citations

Johnson, John P., et al.. (2018). Overrepresentation of pregnancies conceived by artificial reproductive technology in prenatally identified fetuses with Beckwith-Wiedemann syndrome. Journal of Assisted Reproduction and Genetics. 35(6). 985–992. 17 indexed citations

Cummings, Anna, Jacob L. McCauley, Lan Jiang, et al.. (2011). A Genome‐Wide Linkage Screen in the Amish with Parkinson Disease Points to Chromosome 6. Annals of Human Genetics. 75(3). 351–358. 6 indexed citations

Blair, Marcia, Bassel Abou‐Khalil, Amy Crunk, Jonathan L. Haines, & Peter Hedera. (2011). A new locus for autosomal dominant generalized epilepsy associated with mild mental retardation on chromosome 3p. Epilepsia. 52(5). 993–999. 5 indexed citations

Murdock, Deborah G., Jacob L. McCauley, Yvonne M. Bradford, et al.. (2008). A Genome‐wide Scan in an Amish Pedigree with Parkinsonism. Annals of Human Genetics. 72(5). 621–629. 10 indexed citations

McCauley, Jacob L., Amy Crunk, Lynne L. McFarland, et al.. (2006). A genome‐wide linkage analysis of dementia in the Amish. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(2). 160–166. 35 indexed citations

Walt, Joelle M. van der, William K. Scott, Susan Slifer, et al.. (2005). Maternal lineages and Alzheimer disease risk in the Old Order Amish. Human Genetics. 118(1). 115–122. 24 indexed citations

Hedera, Peter, et al.. (2004). Autosomal Dominant Lateral Temporal Epilepsy: Two Families with Novel Mutations in the LGI1 Gene. Epilepsia. 45(3). 218–222. 30 indexed citations

10.

Haines, Jonathan L., Amy Crunk, Lynne L. McFarland, et al.. (2004). S2-01-01 Dementia in mid-Western U.S. amish families. Neurobiology of Aging. 25. S24–S25.

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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