Haley McConkey

1.2k total citations
14 papers, 53 citations indexed

About

Haley McConkey is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Haley McConkey has authored 14 papers receiving a total of 53 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Genetics and 1 paper in Surgery. Recurrent topics in Haley McConkey's work include Epigenetics and DNA Methylation (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Haley McConkey is often cited by papers focused on Epigenetics and DNA Methylation (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Haley McConkey collaborates with scholars based in Canada, United States and Italy. Haley McConkey's co-authors include Bekim Sadiković, Jennifer Kerkhof, Giuseppe Merla, Michael A. Levy, Gabriella Maria Squeo, Maria Rosaria Piemontese, Maria Accadia, Marilena Carmela Di Giacomo, Maria Piccione and Charles E. Schwartz and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Glia.

In The Last Decade

Haley McConkey

10 papers receiving 53 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Haley McConkey Canada	4	38	27	4	4	4	14	53
Ruebena Dawes Australia	4	56 1.5×	24 0.9×	3 0.8×	2 0.5×	4 1.0×	7	71
Chong Y. Park United States	4	29 0.8×	31 1.1×	4 1.0×	3 0.8×	4 1.0×	7	69
Ikhlas Ben Ayed Tunisia	4	22 0.6×	13 0.5×	3 0.8×	4 1.0×	4 1.0×	12	40
Andrey N. Smirnov United States	4	25 0.7×	39 1.4×	4 1.0×	4 1.0×	14 3.5×	5	57
Kathleen Rooney Canada	4	43 1.1×	32 1.2×	2 0.5×	3 0.8×	8 2.0×	7	57
Paul Hale United States	2	35 0.9×	19 0.7×	3 0.8×	6 1.5×	6 1.5×	2	55
Erh‐Chan Yeh Taiwan	2	24 0.6×	12 0.4×	6 1.5×	3 0.8×	6 1.5×	3	38
Carlos Ruiz-Arenas Spain	6	42 1.1×	31 1.1×	3 0.8×	2 0.5×	7 1.8×	8	66
Anna Lehman Canada	4	32 0.8×	30 1.1×	5 1.3×	5 1.3×	2 0.5×	8	66
Geoffroy Delplancq France	5	33 0.9×	28 1.0×	2 0.5×	2 0.5×	4 1.0×	7	56

Countries citing papers authored by Haley McConkey

Since Specialization

Citations

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

Fields of papers citing papers by Haley McConkey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Haley McConkey

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

All Works

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14 of 14 papers shown

Haghshenas, Sadegheh, Michael A. Levy, Raissa Relator, et al.. (2025). Identification of an episignature for the MEF2C-associated syndrome. European Journal of Human Genetics. 34(1). 53–60.

Relator, Raissa, Michael A. Levy, Ankit Verma, et al.. (2025). Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans. Epigenetics & Chromatin. 18(1). 47–47.

McConkey, Haley, et al.. (2025). Astrocytic Chromatin Remodeler ATRX Gates Hippocampal Memory Consolidation Through Metabolic and Synaptic Regulation. Glia. 74(1). e70098–e70098.

McConkey, Haley, Nina Stein, Eric Chater‐Diehl, et al.. (2024). Diagnosis of TET3‐Related Beck–Fahrner Syndrome in an Individual With Chorioretinal and Iris Colobomata Using a DNA Methylation Signature. American Journal of Medical Genetics Part A. 197(2). e63864–e63864.

McConkey, Haley, Matthew J. Cecchini, Christopher J. Howlett, et al.. (2024). Evaluation of HER2 immunohistochemistry expression in non-standard solid tumors from a Single-Institution Prospective Cohort. SHILAP Revista de lepidopterología. 5(5). 1100–1109. 3 indexed citations

Rooney, Kathleen, Sadegheh Haghshenas, Haley McConkey, et al.. (2023). Functional Insight into and Refinement of the Genomic Boundaries of the JARID2-Neurodevelopmental Disorder Episignature. International Journal of Molecular Sciences. 24(18). 14240–14240. 3 indexed citations

Ghaoui, Roula, Thuong Ha, Jennifer Kerkhof, et al.. (2023). Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis. Neuromuscular Disorders. 33(6). 484–489. 3 indexed citations

Haghshenas, Sadegheh, Aidin Foroutan, Michael A. Levy, et al.. (2023). Identification of a DNA methylation signature for Renpenning syndrome (RENS1), a spliceopathy. European Journal of Human Genetics. 31(8). 879–886. 2 indexed citations

Kumps, Candy, Jennifer Kerkhof, Haley McConkey, et al.. (2023). Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown–Rahman syndrome. European Journal of Human Genetics. 31(12). 1350–1354. 2 indexed citations

10.

Squeo, Gabriella Maria, Tommaso Mazza, Stefano Castellana, et al.. (2022). Genome-wide DNA methylation profiling and exome sequencing resolved a long-time misdiagnosed case. Journal of Human Genetics. 67(9). 547–551. 5 indexed citations

11.

Reilly, Jack, Haley McConkey, Jennifer Kerkhof, et al.. (2022). The discovery of the DNA methylation episignature for Duchenne muscular dystrophy. Neuromuscular Disorders. 33(1). 5–14. 3 indexed citations

12.

McConkey, Haley, et al.. (2022). Genetically unresolved case of Rauch-Steindl syndrome diagnosed by its wolf-hirschhorn associated DNA methylation episignature. Frontiers in Cell and Developmental Biology. 10. 4 indexed citations

13.

Haghshenas, Sadegheh, Michael A. Levy, Jennifer Kerkhof, et al.. (2021). Detection of a DNA Methylation Signature for the Intellectual Developmental Disorder, X-Linked, Syndromic, Armfield Type. International Journal of Molecular Sciences. 22(3). 1111–1111. 6 indexed citations

14.

Kerkhof, Jennifer, Gabriella Maria Squeo, Haley McConkey, et al.. (2021). DNA methylation episignature testing improves molecular diagnosis of Mendelian chromatinopathies. Genetics in Medicine. 24(1). 51–60. 22 indexed citations

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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