Erfan Aref‐Eshghi

3.1k citations

48 papers · 1.3k indexed · h-index 21

Co-authors: Bekim Sadiković David I. Rodenhiser Hanxin Lin Peter Ainsworth Glynn Martin Andrew Furey Guangju Zhai Proton Rahman
Topics: Epigenetics and DNA Methylation (13 papers)Osteoarthritis Treatment and Mechanisms (11 papers)Genomics and Rare Diseases (10 papers)
Cited by: Cancer Research Rheumatology Genetics
Journals: PLoS ONE Diabetes Scientific Reports
Partner nations: Canada United States United Kingdom

In The Last Decade

Erfan Aref‐Eshghi

47 papers receiving 1.3k citations

Peers

Countries citing papers authored by Erfan Aref‐Eshghi

Since Specialization

Citations

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

Fields of papers citing papers by Erfan Aref‐Eshghi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Erfan Aref‐Eshghi. 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 Erfan Aref‐Eshghi. The network helps show where Erfan Aref‐Eshghi may publish in the future.

Co-authorship network of co-authors of Erfan Aref‐Eshghi

This figure shows the co-authorship network connecting the top 25 collaborators of Erfan Aref‐Eshghi. A scholar is included among the top collaborators of Erfan Aref‐Eshghi 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 Erfan Aref‐Eshghi. Erfan Aref‐Eshghi 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	Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndrome 2025 ·European Journal of Human Genetics ·Shiyu Luo,Valérie Gailus-Durner,(unknown),Qifei Li,(unknown),Mai‐Lan Ho,Hagar Mor‐Shaked,Orly Elpeleg,Erfan Aref‐Eshghi,(unknown),Klaus Schmitz‐Abe,Casie A. Genetti,Jonathan Picker,Jiahai Shi,(unknown),Tawfeg Ben‐Omran,Helmut Fuchs,Tamar Harel,Martin Hrabě de Angelis,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	0
2	Contribution of DNA methylation profiling to the reclassification of a variant of uncertain significance in the KDM5C gene 2022 ·European Journal of Medical Genetics ·(unknown),Alice Goldenberg,Gaël Nicolas,Pascale Saugier-Véber,Sophie Coutant,Anne Vincent,(unknown),(unknown),Erfan Aref‐Eshghi,Bekim Sadiković,François Lecoquierre	1
3	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
4	The oncogenic roles of NTRK fusions and methods of molecular diagnosis 2021 ·Cancer Genetics ·Erfan Aref‐Eshghi,Fumin Lin,Marilyn M. Li,Yiming Zhong	4
5	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
6	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
7	Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes 2018 ·The American Journal of Human Genetics ·Erfan Aref‐Eshghi,David I. Rodenhiser,Laila C. Schenkel,Hanxin Lin,Cindy Skinner,Peter Ainsworth,Guillaume Paré,Rebecca L. Hood,Dennis E. Bulman,Kristin D. Kernohan,Kym M. Boycott,Philippe M. Campeau,Charles E. Schwartz,Bekim Sadiković	90
8	Genomic DNA Methylation-Derived Algorithm Enables Accurate Detection of Malignant Prostate Tissues 2018 ·Frontiers in Oncology ·Erfan Aref‐Eshghi,Laila C. Schenkel,Peter Ainsworth,Hanxin Lin,David I. Rodenhiser,Jean‐Claude Cutz,Bekim Sadiković	34
9	Peripheral blood epi-signature of Claes-Jensen syndrome enables sensitive and specific identification of patients and healthy carriers with pathogenic mutations in KDM5C 2018 ·Clinical Epigenetics ·Laila C. Schenkel,Erfan Aref‐Eshghi,Cindy Skinner,Peter Ainsworth,Hanxin Lin,Guillaume Paré,David I. Rodenhiser,Charles E. Schwartz,Bekim Sadiković	35
10	Clinical Validation of a Genome-Wide DNA Methylation Assay for Molecular Diagnosis of Imprinting Disorders 2017 ·Journal of Molecular Diagnostics ·Erfan Aref‐Eshghi,Laila C. Schenkel,Hanxin Lin,Cindy Skinner,Peter Ainsworth,Guillaume Paré,Victoria Mok Siu,David I. Rodenhiser,Charles E. Schwartz,Bekim Sadiković	26
11	Identification of Dyslipidemic Patients Attending Primary Care Clinics Using Electronic Medical Record (EMR) Data from the Canadian Primary Care Sentinel Surveillance Network (CPCSSN) Database 2017 ·Journal of Medical Systems ·Erfan Aref‐Eshghi,(unknown),Marshall Godwin,Kris Aubrey‐Bassler,(unknown),(unknown),Shabnam Asghari	15
12	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
13	Emerging Cytokines in Allergic Airway Inflammation: A Genetic Update 2016 ·Current Immunology Reviews ·Karim Daliri,Erfan Aref‐Eshghi,Shahrouz Taranejoo,(unknown),(unknown),(unknown),Mohsen Savaie,(unknown),(unknown),Hassan Askari	2
14	Single and mixed dyslipidaemia in Canadian primary care settings: findings from the Canadian primary care sentinel surveillance network database 2015 ·BMJ Open ·Shabnam Asghari,Erfan Aref‐Eshghi,Marshall Godwin,(unknown),Tyler Williamson,(unknown)	14
15	Gene expression analysis and DNA methylation in the promoter region of matrix metalloproteinase – 13 (MMP-13) and osteoarthritis 2015 ·Osteoarthritis and Cartilage ·Patricia E. Harper,(unknown),Erfan Aref‐Eshghi,Glynn Martin,Andrew Furey,(unknown),Proton Rahman,Guangju Zhai	1
16	Relationship Between Blood Plasma and Synovial Fluid Metabolite Concentrations in Patients with Osteoarthritis 2015 ·The Journal of Rheumatology ·Weidong Zhang,Sergei Likhodii,Erfan Aref‐Eshghi,Yuhua Zhang,Patricia E. Harper,Edward Randell,Roger Green,Glynn Martin,Andrew Furey,Guang Sun,Proton Rahman,Guangju Zhai	45
17	Does the Prevalence of Dyslipidemias Differ between Newfoundland and the Rest of Canada? Findings from the Electronic Medical Records of the Canadian Primary Care Sentinel Surveillance Network 2015 ·Frontiers in Cardiovascular Medicine ·Shabnam Asghari,Erfan Aref‐Eshghi,(unknown),Marshall Godwin,(unknown),Tyler Williamson,(unknown)	28
18	Genome-wide DNA methylation study of hip and knee cartilage reveals embryonic organ and skeletal system morphogenesis as major pathways involved in osteoarthritis 2015 ·BMC Musculoskeletal Disorders ·Erfan Aref‐Eshghi,Yuhua Zhang,Ming Liu,Patricia E. Harper,Glynn Martin,Andrew Furey,Roger Green,Guang Sun,Proton Rahman,Guangju Zhai	36
19	Classification of osteoarthritis phenotypes by metabolomics analysis 2014 ·BMJ Open ·Weidong Zhang,Sergei Likhodii,Yuhua Zhang,Erfan Aref‐Eshghi,Patricia E. Harper,Edward Randell,Roger Green,Glynn Martin,Andrew Furey,Guang Sun,Proton Rahman,Guangju Zhai	93
20	SMAD3 Is Associated with the Total Burden of Radiographic Osteoarthritis: The Chingford Study 2014 ·PLoS ONE ·Erfan Aref‐Eshghi,Yuhua Zhang,Deborah Hart,Ana M. Valdes,Andrew Furey,Glynn Martin,Guang Sun,Proton Rahman,Nigel K. Arden,Tim D. Spector,Guangju Zhai	17

About Erfan Aref‐Eshghi

Erfan Aref‐Eshghi is a scholar working on Cancer Research, Rheumatology and Genetics, having authored 48 papers that have together received 1.3k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (13 papers), Osteoarthritis Treatment and Mechanisms (11 papers) and Genomics and Rare Diseases (10 papers). The work is most often cited by research in Cancer Research (299 citations), Rheumatology (287 citations) and Genetics (397 citations). Erfan Aref‐Eshghi has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Bekim Sadiković, David I. Rodenhiser, Hanxin Lin, Peter Ainsworth, Glynn Martin, Andrew Furey, Guangju Zhai, Proton Rahman, Patricia E. Harper and Laila C. Schenkel. Their work appears in journals such as PLoS ONE, Diabetes and Scientific Reports.

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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