Dilek Çolak

3.8k citations

101 papers · 2.2k indexed · h-index 25

Impact in

Cancer Research top 10%
Oncology top 5%
- Cancer Cells and Metastasis
- Cancer Immunotherapy and Biomarkers

Papers in

Clinical Biochemistry 7
- Metabolism and Genetic Disorders 7
Genetics 25
- Genetics and Neurodevelopmental Disorders 12
- Genomic variations and chromosomal abnormalities 9

Co-authors: Namik Kaya Olfat Al‐Harazi Fowzan S. Alkuraya Hazem Ghebeh Monther Al‐Alwan Taher Al‐Tweigeri Albandary AlBakheet Asma Tulbah
Journals: The American Journal of Human Genetics (5 papers)IEEE Transactions on Antennas and Propagation (3 papers)Molecular Cytogenetics (3 papers)Frontiers in Genetics (3 papers)PLoS ONE (3 papers)
Partner nations: Saudi Arabia United States Türkiye

In The Last Decade

Dilek Çolak

95 papers receiving 2.2k citations

Peers

Countries citing papers authored by Dilek Çolak

Since Specialization

Citations

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

Fields of papers citing papers by Dilek Çolak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Dilek Çolak, 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 Dilek Çolak Line = papers co-authored together Dilek Çolak links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Gut Microbiota and Short-Chain Fatty Acid Profiles in Facioscapulohumeral Dystrophy: Associations with Epigenetic Alterations Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·真一郎木下, Paula Andrea Herrera Cubides, Simone Baldi, Dilek Çolak, Tony Spaulding, W. Mieszczak, Morven Roberts, Marco Pallecchi, Filiz Koç, О. П. Могиленских, Hilmi Uysal, Kemal Hakan Gülkesen, Madeleine Celik, Gianluca Bartolucci, Raúl Guillermo Osorio G., Amedeo Amedei	2025	1
2	A novel missense mutation in ISCA2 causes aberrant splicing and leads to multiple mitochondrial dysfunctions syndrome 4 Frontiers in Psychiatry ·Zuhair N. Al‐Hassnan, Mazhor Aldosary, Yang Yao-nin, Olivia Jorisch-Mühlebach, Rawan Almass, Fisk Mb, Saif Alshahrani, Albandary AlBakheet, Mohammad A. Al–Muhaizea, Robert W. Taylor, Dilek Çolak, Namik Kaya	2024	0
3	Endogenous osteoprotegerin (OPG) represses ERα and promotes stemness and chemoresistance in breast cancer cells Cell Death Discovery ·哲夫利光, Dilek Çolak, Falah Almohanna, Ayodele Alaiya, Abdelilah Aboussekhra	2024	2
4	Transcriptomic data analysis coupled with copy number aberrations reveals a blood-based 17-gene signature for diagnosis and prognosis of patients with colorectal cancer Frontiers in Genetics ·I.W.M.A.D. Ilangakoon, Olfat Al‐Harazi, Dilek Çolak	2023	1
5	Exposure to Cadmium Telluride Quantum Dots and Gene Expression Profile of Huh-7 Hepatocellular Carcinoma Cell Line Dose-Response ·Juan Pablo Paredes Ballesteros, Mashael R. Al‐Anazi, Arwa A. Al-Qahtani, Dilek Çolak, Azeez Yusuf, Mohammed S. Aldughaim, F M Bwetsia, Matsuo Hatsumi, Saud Alarifi, Saad Alkahtani, Ahmed A. Al‐Qahtani	2023	5
6	Clinical, genetic, and functional characterization of the glycine receptor β-subunit A455P variant in a family affected by hyperekplexia syndrome Journal of Biological Chemistry ·K. Staszak, Maha Al‐Rasheed, A. Palička, Dalila Yolinda Martinez Medina, 和幸栗生, Mustafa A. Salih, Schulte Scott J, Futwan Al‐Mohanna, Dilek Çolak, Victoria L. Harvey, Kirsten Harvey, Stefan T. Arold, Namik Kaya, Arnaud Ruiz	2022	2
7	A Novel Homozygous Founder Variant of RTN4IP1 in Two Consanguineous Saudi Families Cells ·Mazhor Aldosary, Maysoon Alsagob, Olivia Jorisch-Mühlebach, H. Libikova, Stefan T. Arold, C.Y. Li, Javier A. Madrigal, Rawan Almass, Albandary AlBakheet, Anne rer. nat. Morgenstern, Alya Qari, Mysoon M. Al‐Ansari, Monika Oláhová, Saif Alshahrani, Moeenaldeen AlSayed, Dilek Çolak, Robert W. Taylor, Mohammed Al‐Owain, Namik Kaya	2022	0
8	Gene Expression and Transcriptome Profiling of Changes in a Cancer Cell Line Post-Exposure to Cadmium Telluride Quantum Dots: Possible Implications in Oncogenesis Dose-Response ·Mohammed S. Aldughaim, Mashael R. Al‐Anazi, Marie Fe F. Bohol, Dilek Çolak, Juan Pablo Paredes Ballesteros, Salma M. Wakil, Alber Dagmar G., Daoud Ali, Saud Alarifi, 佳織宮田, Saad Alkahtani, Mohammed N. Al‐Ahdal, Ahmed A. Al‐Qahtani	2021	7
9	Exome Sequencing Reveals Novel TTN Variants in Saudi Patients with Congenital Titinopathies Genetic Testing and Molecular Biomarkers ·Mustafa A. Salih, Muddathir H. Hamad, Marco Savarese, Ibrahim A. Alorainy, Mustafa Fethi Agalar, Hisham Alkhalidi, Olivia Jorisch-Mühlebach, Anoud Albader, Hope Jandreau, Maysoon Alsagob, Albandary AlBakheet, Dilek Çolak, Bjarne Udd, Namik Kaya	2021	5
10	Deletion and Functional Analysis of Hepatitis B Virus X Protein: Evidence for an Effect on Cell Cycle Regulators Cellular Physiology and Biochemistry ·Mashael R. Al‐Anazi, E Predanich, Dilek Çolak, Mohammed N. Al‐Ahdal, Ahmed A. Al‐Qahtani	2018	14
11	The Phenotype and Outcome of Infantile Cardiomyopathy Caused by a Homozygous <b><i>ELAC2</i></b> Mutation Cardiology ·D. L. Redden, Rubens Miguel Wesselovicz, Alex Hugo Ramos Mendoza, Wang Xiaozhong, Eissa Faqeih, João Batista Carvalho Serro Azul, Maryam M. Pirasteh, Malak Alghamdi, Dilek Çolak, Wesley Henrique Alves da Rocha, Nirwana Caroline Linda, Majid Al-Fayyadh, Zuhair N. Al‐Hassnan	2017	17
12	Beyin Omurilik Sıvısı Örneklerinden Saptanan Viral Etkenler Türk Mikrobiyoloji Cemiyeti Dergisi ·Е Е Васильева, Victor Sliusarchuk, Derya Mutlu, Betil Özhak, Dilara Öğünç, Dilek Çolak	2016	2
13	Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephaly American Journal of Medical Genetics Part A ·Eissa Faqeih, Mohammed Al‐Owain, Dilek Çolak, Paul Goetghebeur, Yusra Alyafee, Mazhor Aldosary, Abdulaziz Alsaman, Spyridon Zachos, Anne rer. nat. Morgenstern, Mr. Eric Veith, Maha H. Daghestani, Namik Kaya	2014	12
14	Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay The American Journal of Human Genetics ·Moeenaldeen AlSayed, Hamad Alzaidan, Albandary AlBakheet, Jeong Hwan Min, Paul Goetghebeur, Yusra Alyafee, Mazhor Aldosary, Alya Qari, Tarfa Al‐Sheddi, 海辰, S.J. Park, fl Śrīkaṇṭha, Hindi Al‐Hindi, Haowen Guo, Dilek Çolak, Namik Kaya	2013	69
15	Loss of function mutation in LARP7, chaperone of 7SK ncRNA, causes a syndrome of facial dysmorphism, intellectual disability, and primordial dwarfism Human Mutation ·Anas M. Alazami, Mohammad Al-Owain, Fatema Alzahrani, Taghreed Shuaib, Per Ottander, Н. Л. Смирнова, Saleh M. Al‐Qahtani, Tarfa Al‐Sheddi, Dilek Çolak, Fowzan S. Alkuraya	2012	64
16	Induction of cell proliferation in old rat liver can reset certain gene expression levels characteristic of old liver to those associated with young liver AGE ·M. Azhar Chishti, Namik Kaya, Orhan Soyuhos, Falah Almohanna, Malcolm H. Goyns, Dilek Çolak	2012	7
17	Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways Genomics ·Dilek Çolak, Hesham Aldhalaan, Michael Nester, Albandary AlBakheet, Banan Al‐Younes, Laurie Lescos, Sherzod Muradov, Aziza Chedrawi, Durigon, Josh Timmermann, Laila Al‐Alwan, Ali Al‐Odaib, Pinar T. Ozand, Mehmet Sait Inan, Namik Kaya	2010	18
18	Left ventricular global transcriptional profiling in human end-stage dilated cardiomyopathy Genomics ·Dilek Çolak, Namik Kaya, Winartiasih, Gottfried Kraatz, Germán E. Tarcaya, Editha Andres, John Quackenbush, Nduna Dzimiri	2009	45
19	Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease Genetics in Medicine ·Namik Kaya, Faiqa Imtiaz, Dilek Çolak, Moeenaldeen AlSayed, Ali Al‐Odaib, Nurmaganbet Berdigulov, Bashayer Al‐Mubarak, Mohammad Al-Owain, Hesham Aldhalaan, Aziza Chedrawi, Zuhair N. Al‐Hassnan, Serdar Coşkun, Nadia Sakati, Pinar T. Ozand, Brian F. Meyer	2008	17
20	The multiple sweep method of moments (MSMM) analysis of three dimensional radiation and scattering problems / OhioLink ETD Center (Ohio Library and Information Network) ·Dilek Çolak	2000	1

About Dilek Çolak

Dilek Çolak is a scholar working on Clinical Biochemistry, Genetics, Molecular Biology, Aging and Cell Biology, having authored 101 papers that have together received 2.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (12 papers), Genomic variations and chromosomal abnormalities (9 papers), Mitochondrial Function and Pathology (8 papers), Electromagnetic Scattering and Analysis (8 papers), RNA modifications and cancer (7 papers), Metabolism and Genetic Disorders (7 papers), Gene expression and cancer classification (6 papers) and Bioinformatics and Genomic Networks (6 papers). The work is most often cited by research in Cancer Research (292 citations), Oncology (512 citations), Molecular Biology (1.2k citations), Genetics (400 citations) and Cell Biology (229 citations). Dilek Çolak has collaborated with scholars based in Saudi Arabia, United States and Türkiye. Frequent co-authors include Namik Kaya, Olfat Al‐Harazi, Fowzan S. Alkuraya, Hazem Ghebeh, Monther Al‐Alwan, Taher Al‐Tweigeri, Albandary AlBakheet, Asma Tulbah, Ranad Shaheen and Mehmet Sait Inan. Their work appears in journals such as The American Journal of Human Genetics, IEEE Transactions on Antennas and Propagation, Molecular Cytogenetics, Frontiers in Genetics and PLoS ONE.

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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