Jennifer Kerkhof

2.5k total citations
41 papers, 458 citations indexed

About

Jennifer Kerkhof is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Jennifer Kerkhof has authored 41 papers receiving a total of 458 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 24 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Jennifer Kerkhof's work include Genomics and Rare Diseases (17 papers), Epigenetics and DNA Methylation (14 papers) and Genetics and Neurodevelopmental Disorders (11 papers). Jennifer Kerkhof is often cited by papers focused on Genomics and Rare Diseases (17 papers), Epigenetics and DNA Methylation (14 papers) and Genetics and Neurodevelopmental Disorders (11 papers). Jennifer Kerkhof collaborates with scholars based in Canada, United States and Netherlands. Jennifer Kerkhof's co-authors include Bekim Sadiković, Peter Ainsworth, Alan Stuart, Hanxin Lin, Erfan Aref‐Eshghi, Joyce B. J. van Meurs, Fernando Rivadeneira, André G. Uitterlinden, Huibert A. P. Pols and Albert Hofman and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, The FASEB Journal and International Journal of Molecular Sciences.

In The Last Decade

Jennifer Kerkhof

36 papers receiving 447 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jennifer Kerkhof Canada	11	249	212	79	72	49	41	458
Malwina Czarny‐Ratajczak Poland	12	187 0.8×	182 0.9×	63 0.8×	137 1.9×	52 1.1×	23	470
Kit San Yeung Hong Kong	13	252 1.0×	245 1.2×	30 0.4×	44 0.6×	57 1.2×	29	529
Patricio Barros‐Núñez Mexico	15	359 1.4×	302 1.4×	54 0.7×	38 0.5×	28 0.6×	71	688
Gundula Leschik Germany	9	380 1.5×	234 1.1×	49 0.6×	123 1.7×	29 0.6×	11	608
Lauréane Mittaz Switzerland	10	211 0.8×	180 0.8×	63 0.8×	76 1.1×	40 0.8×	10	586
Shaohong Cheng United States	14	278 1.1×	86 0.4×	92 1.2×	63 0.9×	18 0.4×	19	410
Youn Hee Jee United States	13	253 1.0×	173 0.8×	99 1.3×	52 0.7×	30 0.6×	30	506
Emilia Ballarè Italy	13	347 1.4×	213 1.0×	58 0.7×	61 0.8×	114 2.3×	14	757
Suna Önengüt United States	11	396 1.6×	120 0.6×	88 1.1×	19 0.3×	30 0.6×	11	551
Elke Piters Belgium	11	418 1.7×	190 0.9×	21 0.3×	46 0.6×	33 0.7×	19	543

Countries citing papers authored by Jennifer Kerkhof

Since Specialization

Citations

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

Fields of papers citing papers by Jennifer Kerkhof

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jennifer Kerkhof

This figure shows the co-authorship network connecting the top 25 collaborators of Jennifer Kerkhof. A scholar is included among the top collaborators of Jennifer Kerkhof 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 Jennifer Kerkhof. Jennifer Kerkhof 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

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.

Campbell, Christopher, Leigh Demain, Sarah Jenkinson, et al.. (2025). Evaluating DNA methylation episignatures as a first-tier diagnostic test in individuals with suspected genetic disorders. European Journal of Human Genetics. 34(2). 296–299.

Vitobello, Antonio, Bekim Sadiković, Juliette Albuisson, et al.. (2025). Abnormal DNA Methylation Profile Suggests the Extension of the Clinical Spectrum of the SETD2‐Related Disorders to a Syndromic Multiple Tumor Phenotype. American Journal of Medical Genetics Part A. 197(7). e64043–e64043. 1 indexed citations

Sadiković, Bekim, Jennifer Kerkhof, Charles E. Schwartz, et al.. (2025). A novel KDM5C variant corrects a previously erroneous diagnosis. European Journal of Medical Genetics. 74. 104997–104997.

Vossaert, Liesbeth, Robin S. Fletcher, Matthew L. Tedder, et al.. (2024). Recurrent carotid paragangliomas in a syndromic patient with a heterozygous missense variant in DNA Methyltransferase 3 Alpha. American Journal of Medical Genetics Part A. 197(1). e63849–e63849. 1 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

Bukvić, Nenad, Massimiliano Chetta, Rosanna Bagnulo, et al.. (2023). What Have We Learned from Patients Who Have Arboleda-Tham Syndrome Due to a De Novo KAT6A Pathogenic Variant with Impaired Histone Acetyltransferase Function? A Precise Clinical Description May Be Critical for Genetic Testing Approach and Final Diagnosis. Genes. 14(1). 165–165. 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

Hsia, Cyrus C., Laila C. Schenkel, Benjamin D. Hedley, et al.. (2022). Clinical Utility of Implementing a Frontline NGS-Based DNA and RNA Fusion Panel Test for Patients with Suspected Myeloid Malignancies. Molecular Diagnosis & Therapy. 26(3). 333–343. 8 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.

Rooney, Kathleen, Michael A. Levy, Sadegheh Haghshenas, et al.. (2021). Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome. International Journal of Molecular Sciences. 22(16). 8611–8611. 13 indexed citations

12.

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

13.

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

14.

Kawata, Eri, Alejandro Lazo‐Langner, Anargyros Xenocostas, et al.. (2020). Clinical value of next‐generation sequencing compared to cytogenetics in patients with suspected myelodysplastic syndrome. British Journal of Haematology. 192(4). 729–736. 8 indexed citations

15.

Tarnopolsky, Mark A., Jennifer Kerkhof, Alan Stuart, et al.. (2020). Bone marrow‐derived mitochondrial DNA has limited capacity for inter‐tissue transfer in vivo. The FASEB Journal. 34(7). 9297–9306. 5 indexed citations

16.

Volodarsky, Michael, Jennifer Kerkhof, Alan Stuart, et al.. (2020). Comprehensive genetic sequence and copy number analysis for Charcot-Marie-Tooth disease in a Canadian cohort of 2517 patients. Journal of Medical Genetics. 58(4). 284–288. 19 indexed citations

17.

Aref‐Eshghi, Erfan, Danielle K. Bourque, Jennifer Kerkhof, et al.. (2019). Genome‐wide DNA methylation and RNA analyses enable reclassification of two variants of uncertain significance in a patient with clinical Kabuki syndrome. Human Mutation. 40(10). 1684–1689. 19 indexed citations

18.

Ramadža, Danijela Petković, Kristina Potočki, Kamelija Žarković, et al.. (2018). Hypogammaglobulinemia and imaging features in a patient with infantile free sialic acid storage disease (ISSD) and a novel mutation in the SLC17A5 gene. Journal of Pediatric Endocrinology and Metabolism. 31(10). 1155–1159. 1 indexed citations

19.

Kerkhof, Jennifer, Laila C. Schenkel, Jack Reilly, et al.. (2017). Clinical Validation of Copy Number Variant Detection from Targeted Next-Generation Sequencing Panels. Journal of Molecular Diagnostics. 19(6). 905–920. 94 indexed citations

20.

Schenkel, Laila C., Jennifer Kerkhof, Alan Stuart, et al.. (2016). Clinical Next-Generation Sequencing Pipeline Outperforms a Combined Approach Using Sanger Sequencing and Multiplex Ligation-Dependent Probe Amplification in Targeted Gene Panel Analysis. Journal of Molecular Diagnostics. 18(5). 657–667. 43 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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