Bekim Sadiković

6.9k citations

130 papers · 2.7k indexed · h-index 30

Cancer Research top 2%
- Cancer Genomics and Diagnostics 12
Genetics top 2%
- Genomics and Rare Diseases 35
- Genetics and Neurodevelopmental Disorders 26
- Genomic variations and chromosomal abnormalities 14
- Genetic Syndromes and Imprinting 10
- Myeloproliferative Neoplasms: Diagnosis and Treatment 10
Molecular Biology top 5%
- Epigenetics and DNA Methylation 49
- RNA modifications and cancer 10
Health Informatics top 5%
Clinical Biochemistry top 5%

Co-authors: Maria Zieleńska Jeremy A. Squire David I. Rodenhiser Erfan Aref‐Eshghi Khaldoun Al‐Romaih Peter Ainsworth Laila C. Schenkel Guillaume Paré
Cited by: Cancer Research Genetics Molecular Biology
Journals: Journal of Biological Chemistry (1 paper)SHILAP Revista de lepidopterología (1 paper)Blood (4 papers)
Partner nations: Canada United States Netherlands

In The Last Decade

Bekim Sadiković

116 papers receiving 2.7k citations

Peers

Countries citing papers authored by Bekim Sadiković

Since Specialization

Citations

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

Fields of papers citing papers by Bekim Sadiković

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Bekim Sadiković, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Bekim Sadiković Line = papers co-authored together Bekim Sadiković links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	SCN1A pathogenic variants do not have a distinctive blood‐derived DNA methylation signature Epilepsia ·Christy W. LaFlamme,Karim Karimi,Cassandra Rastin,Edith P. Almanza Fuerte,Talia Allan,Sophie Russ-Hall,Amy Schneider,Daniel Stobo,Gaëtan Lesca,Joseph D. Symonds,Andreas Brunklaus,Lynette G. Sadleir,Ingrid E. Scheffer,Bekim Sadiković,Heather C. Mefford	2025	0
2	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 ·Marie Lucain,Antonio Vitobello,Bekim Sadiković,Juliette Albuisson,Léa Gaudillat,Martin Chevarin,Julien Maraval,Christel Thauvin‐Robinet,Jennifer Kerkhof,Christophe Philippe,Sophie Nambot,Laurence Faivre	2025	1
3	Identification of an episignature for the MEF2C-associated syndrome European Journal of Human Genetics ·Ananília Silva,Sadegheh Haghshenas,Liselot van der Laan,Michael A. Levy,Raissa Relator,Haley McConkey,Jennifer Kerkhof,Steve A. Skinner,Laurence Faivre,James Lespinasse,Antonio Vitobello,Irene Valenzuela,Ingrid E. Scheffer,Sophie Russ-Hall,Kenneth A. Myers,Matthew L. Tedder,Bekim Sadiković,Jessica A. Cooley Coleman	2025	0
4	Leaving no patient behind! Expert recommendation in the use of innovative technologies for diagnosing rare diseases Orphanet Journal of Rare Diseases ·Clara D.M. van Karnebeek,Anne O’Donnell‐Luria,Gareth Baynam,Anaı̈s Baudot,Tudor Groza,Judith Jans,Timo Lassmann,Mary Catherine V. Letinturier,Stephen B. Montgomery,Peter N Robinson,Stefaan Sansen,Ruty Mehrian‐Shai,Charles A. Steward,Kenjiro Kosaki,Patricia Durao,Bekim Sadiković	2024	7
5	An Approach to the Investigation of Thrombocytosis: Differentiating between Essential Thrombocythemia and Secondary Thrombocytosis Advances in Hematology ·Ala Almanaseer,Benjamin Chin‐Yee,Jenny Ho,Alejandro Lazo‐Langner,Laila C. Schenkel,Pratibha Bhai,Bekim Sadiković,Ian Chin‐Yee,Cyrus C. Hsia	2024	1
6	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 ·Nenad Bukvić,Massimiliano Chetta,Rosanna Bagnulo,Valentina Leotta,Antonino Pantaleo,Orazio Palumbo,Pietro Palumbo,Maria Oro,Maria Rivieccio,Nicola Laforgia,Marta De Rinaldis,Alessandra Rosati,Jennifer Kerkhof,Bekim Sadiković,Nicoletta Resta	2023	3
7	Genotypic analysis of a large cohort of patients with suspected atypical hemolytic uremic syndrome Journal of Molecular Medicine ·Dervla M. Connaughton,Pratibha Bhai,Paul Isenring,Mohammed Mahdi,Bekim Sadiković,Laila C. Schenkel	2023	2
8	Complexity in Genetic Epilepsies: A Comprehensive Review International Journal of Molecular Sciences ·Cassandra Rastin,Laila C. Schenkel,Bekim Sadiković	2023	13
9	Functional Insight into and Refinement of the Genomic Boundaries of the JARID2-Neurodevelopmental Disorder Episignature International Journal of Molecular Sciences ·Liselot van der Laan,Kathleen Rooney,Sadegheh Haghshenas,Ananília Silva,Haley McConkey,Raissa Relator,Michael A. Levy,Irene Valenzuela,Laura Trujillano,Amaia Lasa‐Aranzasti,Berta Campos,Neus Castells,Eline A. Verberne,Saskia M. Maas,Mariëlle Alders,Marcel M. A. M. Mannens,Mieke M. van Haelst,Bekim Sadiković,Peter Henneman	2023	3
10	Mutational Landscape of Patients Referred for Elevated Hemoglobin Level Current Oncology ·Pratibha Bhai,Benjamin Chin‐Yee,Victor Pope,Ian Cheong,Maxim Matyashin,Michael A. Levy,Aidin Foroutan,Alan Stuart,Cyrus C. Hsia,Hanxin Lin,Bekim Sadiković,Ian Chin‐Yee	2022	0
11	DNA methylation episignatures: insight into copy number variation Epigenomics ·Liselot van der Laan,Kathleen Rooney,Tessa MA Trooster,Marcel M. A. M. Mannens,Bekim Sadiković,Peter Henneman	2022	12
12	Incidental findings from cancer next generation sequencing panels npj Genomic Medicine ·Nika Maani,Karen Panabaker,Jeanna McCuaig,Kathleen Buckley,Kara Semotiuk,Kirsten M. Farncombe,Peter Ainsworth,Seema Panchal,Bekim Sadiković,Susan Randall Armel,Hanxin Lin,Raymond H. Kim	2021	13
13	Reducing cytogenetic testing in the era of next generation sequencing: Are we choosing wisely? International Journal of Laboratory Hematology ·Eri Kawata,Benjamin D. Hedley,Benjamin Chin‐Yee,Anargyros Xenocostas,Alejandro Lazo‐Langner,Cyrus C. Hsia,Kang Howson‐Jan,Ping Yang,Michael A. Levy,Stephanie Santos,Pratibha Bhai,Christopher J. Howlett,Hanxin Lin,Mike Kadour,Bekim Sadiković,Ian Chin‐Yee	2021	2
14	Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome International Journal of Molecular Sciences ·Kathleen Rooney,Michael A. Levy,Sadegheh Haghshenas,Jennifer Kerkhof,Daniela Rogaia,Maria Giovanna Tedesco,Valentina Imperatore,Amedea Mencarelli,Gabriella Maria Squeo,Eleonora Di Venere,Giuseppe Di Cara,Alberto Verrotti,Giuseppe Merla,Matthew L. Tedder,Barbara R. DuPont,Bekim Sadiković,Paolo Prontera	2021	13
15	Discovery of a novel CHD7 CHARGE syndrome variant by integrated omics analyses American Journal of Medical Genetics Part A ·Jorge L. Granadillo,Daniel Wegner,Alexander J. Paul,Marcia Willing,Kathleen Sisco,Matthew L. Tedder,Bekim Sadiković,Jennifer Wambach,Dustin Baldridge,F. Sessions Cole,(unknown)	2020	9
16	Genome‐wide DNA methylation and RNA analyses enable reclassification of two variants of uncertain significance in a patient with clinical Kabuki syndrome Human Mutation ·Erfan Aref‐Eshghi,Danielle K. Bourque,Jennifer Kerkhof,Deanna Alexis Carere,Peter Ainsworth,Bekim Sadiković,Christine M. Armour,Hanxin Lin	2019	19
17	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 ·Tamara Žigman,Danijela Petković Ramadža,Mario Lušić,Marija Zekušić,Dorotea Ninković,Danilo Gardijan,Kristina Potočki,Lana Omerza,Lucija Beljan,Kamelija Žarković,Jennifer Kerkhof,Marija Ljubojević,Monique de Sain-van der Velden,Jurica Vuković,Ksenija Fumić,Bekim Sadiković,Ivo Barić	2018	1
18	Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome Epigenetics & Chromatin ·Laila C. Schenkel,Kristin D. Kernohan,Arran McBride,Reina Ditta,Amanda Hodge,Peter Ainsworth,David I. Rodenhiser,Guillaume Paré,Nathalie G. Bérubé,Cindy Skinner,Kym M. Boycott,Charles E. Schwartz,Bekim Sadiković	2017	42
19	NLRP7 affects trophoblast lineage differentiation, binds to overexpressed YY1 and alters CpG methylation Human Molecular Genetics ·Sangeetha Mahadevan,Shu Wen,Ying-Wooi Wan,Hsiu-Huei Peng,Subhendu Kumar Otta,Zhandong Liu,Michelina Iacovino,Elisabeth Mahen,Michael Kyba,Bekim Sadiković,Ignatia B. Van den Veyver	2013	52
20	Genome-wide H3K9 Histone Acetylation Profiles Are Altered in Benzopyrene-treated MCF7 Breast Cancer Cells Journal of Biological Chemistry ·Bekim Sadiković,Joseph Andrews,David M. Carter,J. Wesley Robinson,David I. Rodenhiser	2007	70

About Bekim Sadiković

Bekim Sadiković is a scholar working on Genetics, Hematology and Genetics, having authored 130 papers that have together received 2.7k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (49 papers), Genomics and Rare Diseases (35 papers), Genetics and Neurodevelopmental Disorders (26 papers), Genomic variations and chromosomal abnormalities (14 papers), Cancer Genomics and Diagnostics (12 papers), Genetic Syndromes and Imprinting (10 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (10 papers) and RNA modifications and cancer (10 papers). The work is most often cited by research in Cancer Research (731 citations), Genetics (813 citations) and Molecular Biology (1.8k citations). Bekim Sadiković has collaborated with scholars based in Canada, United States and Netherlands. Frequent co-authors include Maria Zieleńska, Jeremy A. Squire, David I. Rodenhiser, Erfan Aref‐Eshghi, Khaldoun Al‐Romaih, Peter Ainsworth, Laila C. Schenkel, Guillaume Paré, Hanxin Lin and Maisa Yoshimoto. Their work appears in journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Blood.

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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