Jennifer Kerkhof

2.5k citations

41 papers · 458 indexed · h-index 11

Co-authors: Bekim Sadiković Peter Ainsworth Alan Stuart Erfan Aref‐Eshghi Hanxin Lin Albert Hofman Huibert A. P. Pols Fernando Rivadeneira
Topics: Genomics and Rare Diseases (17 papers)Epigenetics and DNA Methylation (14 papers)Genetics and Neurodevelopmental Disorders (11 papers)
Cited by: Genetics Cancer Research Rheumatology
Journals: The Journal of Clinical Endocrinology & Metabolism The FASEB Journal International Journal of Molecular Sciences
Partner nations: Canada United States Netherlands

In The Last Decade

Jennifer Kerkhof

36 papers receiving 447 citations

Peers

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

#	Work	Indexed citations
1	Abnormal DNA Methylation Profile Suggests the Extension of the Clinical Spectrum of the SETD2‐Related Disorders to a Syndromic Multiple Tumor Phenotype 2025 ·American Journal of Medical Genetics Part A ·(unknown),Antonio Vitobello,Bekim Sadiković,Juliette Albuisson,(unknown),Martin Chevarin,(unknown),(unknown),Jennifer Kerkhof,(unknown),Sophie Nambot,Laurence Faivre	1
2	Identification of an episignature for the MEF2C-associated syndrome 2025 ·European Journal of Human Genetics ·(unknown),Sadegheh Haghshenas,(unknown),Michael A. Levy,Raissa Relator,Haley McConkey,Jennifer Kerkhof,Steve A. Skinner,Laurence Faivre,James Lespinasse,Antonio Vitobello,Irene Valenzuela,Ingrid E. Scheffer,(unknown),Kenneth A. Myers,Matthew L. Tedder,Bekim Sadiković,(unknown)	0
3	Evaluating DNA methylation episignatures as a first-tier diagnostic test in individuals with suspected genetic disorders 2025 ·European Journal of Human Genetics ·(unknown),Christopher Campbell,(unknown),(unknown),(unknown),Leigh Demain,Sarah Jenkinson,Sarah K. Hilton,Michael A. Levy,Jennifer Kerkhof,David Gokhale,Bekim Sadiković,Siddharth Banka	0
4	Discovery of a DNA methylation episignature as a molecular biomarker for fetal alcohol syndrome 2025 ·Genetics in Medicine ·(unknown),Raissa Relator,Irene Valenzuela,Adri N. Mul,Mariëlle Alders,Michael A. Levy,Jennifer Kerkhof,(unknown),Anna M. Cueto‐González,(unknown),(unknown),Marcel M. A. M. Mannens,Mieke M. van Haelst,Eduardo F. Tizzano,Bekim Sadiković,Peter Henneman	0
5	A novel KDM5C variant corrects a previously erroneous diagnosis 2025 ·European Journal of Medical Genetics ·(unknown),Bekim Sadiković,Jennifer Kerkhof,Charles E. Schwartz,Roger E. Stevenson,Cindy Skinner,Melanie May,Michael J. Friez,Robert Roger Lebel	0
6	The missing link: ARID1B non-truncating variants causing Coffin-Siris syndrome due to protein aggregation 2024 ·Human Genetics ·(unknown),(unknown),Philipp Kirchner,Andreas Winterpacht,(unknown),Mariëlle Alders,Jennifer Kerkhof,Arif B. Ekici,Heinrich Sticht,Bekim Sadiković,André Reis,Georgia Vasileiou	1
7	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 2023 ·Genes ·Nenad Bukvić,Massimiliano Chetta,Rosanna Bagnulo,(unknown),(unknown),Orazio Palumbo,Pietro Palumbo,(unknown),(unknown),Nicola Laforgia,Marta De Rinaldis,Alessandra Rosati,Jennifer Kerkhof,Bekim Sadiković,Nicoletta Resta	3
8	Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis 2023 ·Neuromuscular Disorders ·Roula Ghaoui,Thuong Ha,Jennifer Kerkhof,Haley McConkey,Song Gao,Milena Babic,Robert A. King,Gianina Ravenscroft,Barbara Koszyca,Sophia Otto,Nigel G. Laing,Hamish S. Scott,Bekim Sadiković,Karin S. Kassahn	3
9	Genome-wide DNA methylation profiling and exome sequencing resolved a long-time misdiagnosed case 2022 ·Journal of Human Genetics ·(unknown),Gabriella Maria Squeo,(unknown),(unknown),Tommaso Mazza,Stefano Castellana,Jennifer Kerkhof,Haley McConkey,Bekim Sadiković,Lorenzo Sinibaldi,M. Cristina Digilio,Giuseppe Merla	5
10	Clinical Utility of Implementing a Frontline NGS-Based DNA and RNA Fusion Panel Test for Patients with Suspected Myeloid Malignancies 2022 ·Molecular Diagnosis & Therapy ·(unknown),Cyrus C. Hsia,Laila C. Schenkel,Benjamin D. Hedley,Michael A. Levy,Jennifer Kerkhof,(unknown),Alan Stuart,Hanxin Lin,(unknown),(unknown),Ping Yang,Anargyros Xenocostas,Ian Chin‐Yee,Bekim Sadiković	8
11	Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome 2021 ·International Journal of Molecular Sciences ·Kathleen Rooney,Michael A. Levy,Sadegheh Haghshenas,Jennifer Kerkhof,Daniela Rogaia,(unknown),(unknown),Amedea Mencarelli,Gabriella Maria Squeo,(unknown),Giuseppe Di Cara,Alberto Verrotti,Giuseppe Merla,Matthew L. Tedder,Barbara R. DuPont,Bekim Sadiković,Paolo Prontera	13
12	Detection of a DNA Methylation Signature for the Intellectual Developmental Disorder, X-Linked, Syndromic, Armfield Type 2021 ·International Journal of Molecular Sciences ·Sadegheh Haghshenas,Michael A. Levy,Jennifer Kerkhof,Erfan Aref‐Eshghi,Haley McConkey,Tuğçe B. Balcı,Victoria Mok Siu,Cindy Skinner,Roger E. Stevenson,Bekim Sadiković,Charles E. Schwartz	6
13	DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome 2021 ·Clinical Epigenetics ·Laila C. Schenkel,Erfan Aref‐Eshghi,Kathleen Rooney,Jennifer Kerkhof,Michael A. Levy,Hannah McConkey,R. Curtis Rogers,Katy Phelan,Sara M. Sarasua,(unknown),Rini Pauly,Luigi Boccuto,Barbara R. DuPont,Gerarda Cappuccio,Nicola Brunetti‐Pierri,Charles E. Schwartz,Bekim Sadiković	21
14	Clinical value of next‐generation sequencing compared to cytogenetics in patients with suspected myelodysplastic syndrome 2020 ·British Journal of Haematology ·Eri Kawata,Alejandro Lazo‐Langner,Anargyros Xenocostas,Cyrus C. Hsia,Kang Howson‐Jan,(unknown),(unknown),Ping Yang,(unknown),Michael A. Levy,Christopher J. Howlett,Alan Stuart,Jennifer Kerkhof,(unknown),Hanxin Lin,Bekim Sadiković,Ian Chin‐Yee	8
15	Genome‐wide DNA methylation and RNA analyses enable reclassification of two variants of uncertain significance in a patient with clinical Kabuki syndrome 2019 ·Human Mutation ·Erfan Aref‐Eshghi,Danielle K. Bourque,Jennifer Kerkhof,Deanna Alexis Carere,Peter Ainsworth,Bekim Sadiković,Christine M. Armour,Hanxin Lin	19
16	Hypogammaglobulinemia and imaging features in a patient with infantile free sialic acid storage disease (ISSD) and a novel mutation in the SLC17A5 gene 2018 ·Journal of Pediatric Endocrinology and Metabolism ·(unknown),Danijela Petković Ramadža,(unknown),(unknown),(unknown),(unknown),Kristina Potočki,(unknown),(unknown),Kamelija Žarković,Jennifer Kerkhof,Marija Ljubojević,(unknown),(unknown),Ksenija Fumić,Bekim Sadiković,Ivo Barić	1
17	Clinical Validation of Copy Number Variant Detection from Targeted Next-Generation Sequencing Panels 2017 ·Journal of Molecular Diagnostics ·Jennifer Kerkhof,Laila C. Schenkel,Jack Reilly,(unknown),Erfan Aref‐Eshghi,Alan Stuart,C. Anthony Rupar,Paul C. Adams,Robert A. Hegele,Hanxin Lin,David I. Rodenhiser,Joan H.M. Knoll,Peter Ainsworth,Bekim Sadiković	94
18	Clinical Next-Generation Sequencing Pipeline Outperforms a Combined Approach Using Sanger Sequencing and Multiplex Ligation-Dependent Probe Amplification in Targeted Gene Panel Analysis 2016 ·Journal of Molecular Diagnostics ·Laila C. Schenkel,Jennifer Kerkhof,Alan Stuart,Jack Reilly,Barry Eng,(unknown),(unknown),Christopher J. Howlett,(unknown),Joan H.M. Knoll,Peter Ainsworth,John S. Waye,Bekim Sadiković	43
19	Genetic variation in the GDF5 region is associated with osteoarthritis, height, hip axis length and fracture risk: the Rotterdam study 2008 ·Annals of the Rheumatic Diseases ·(unknown),Fernando Rivadeneira,Jennifer Kerkhof,Albert Hofman,Huibert A. P. Pols,André G. Uitterlinden,Joyce B. J. van Meurs	57
20	Radiographic osteoarthritis at three joint sites and FRZB, LRP5, and LRP6 polymorphisms in two population-based cohorts 2008 ·Osteoarthritis and Cartilage ·Jennifer Kerkhof,André G. Uitterlinden,Ana M. Valdes,Deborah Hart,Fernando Rivadeneira,Mila Jhamai,Albert Hofman,Huibert A. P. Pols,Sita Bierma‐Zeinstra,Tim D. Spector,Joyce B. J. van Meurs	41

About Jennifer Kerkhof

Jennifer Kerkhof is a scholar working on Genetics, Pharmacy and Cancer Research, having authored 41 papers that have together received 458 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (17 papers), Epigenetics and DNA Methylation (14 papers) and Genetics and Neurodevelopmental Disorders (11 papers). The work is most often cited by research in Genetics (212 citations), Cancer Research (79 citations) and Rheumatology (72 citations). Jennifer Kerkhof has collaborated with scholars based in Canada, United States and Netherlands. Frequent co-authors include Bekim Sadiković, Peter Ainsworth, Alan Stuart, Erfan Aref‐Eshghi, Hanxin Lin, Albert Hofman, Huibert A. P. Pols, Fernando Rivadeneira, Joyce B. J. van Meurs and Laila C. Schenkel. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, The FASEB Journal and International Journal of Molecular Sciences.

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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