Tuğçe B. Balcı

1.9k citations

30 papers · 531 indexed · h-index 12

Co-authors: Jason N. Berman Graham Dellaire Udo F. Hartwig Martina Konantz Maya C. André Claudia Lengerke David A. Dyment Sahar Da’as
Topics: Genomics and Rare Diseases (7 papers)Epigenetics and DNA Methylation (6 papers)Genomic variations and chromosomal abnormalities (5 papers)
Cited by: Genetics Cell Biology Hematology
Journals: Journal of Clinical InvestigationSHILAP Revista de lepidopterologíaBlood
Partner nations: Canada United States Türkiye

In The Last Decade

Tuğçe B. Balcı

26 papers receiving 525 citations

Peers

Countries citing papers authored by Tuğçe B. Balcı

Since Specialization

Citations

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

Fields of papers citing papers by Tuğçe B. Balcı

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tuğçe B. Balcı. 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 Tuğçe B. Balcı. The network helps show where Tuğçe B. Balcı may publish in the future.

Co-authorship network of co-authors of Tuğçe B. Balcı

This figure shows the co-authorship network connecting the top 25 collaborators of Tuğçe B. Balcı. A scholar is included among the top collaborators of Tuğçe B. Balcı 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 Tuğçe B. Balcı. Tuğçe B. Balcı 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	Diagnostic Utility of Exome Data Reanalysis After In Silico Multi‐Gene Panels or Clinical Exome Testing for Patients With Epilepsy and Developmental Delay/Intellectual Disability: A Retrospective Cohort Study 2025 ·Clinical Genetics ·Alexanne Cuillerier,(unknown),(unknown),(unknown),Christine M. Armour,(unknown),Danielle K. Bourque,(unknown),Joanna Lazier,Sarah L. Sawyer,Maha Saleh,Chitra Prasad,Victoria Mok Siu,Kym M. Boycott,(unknown),David A. Dyment,Tuğçe B. Balcı	0
2	Sexual dimorphism in SMAD3 pathogenic variant-harbouring individuals 2025 ·Journal of Medical Genetics ·Julie Richer,(unknown),Sharan Goobie,(unknown),Ingrid M.B.H. van de Laar,Judith M.A. Verhagen,Marja W. Wessels,Jolien W. Roos‐Hesselink,Ilse Luyckx,(unknown),Michael Chu,Anne‐Marie Laberge,Bekim Sadiković,Tuğçe B. Balcı,Aline Verstraeten,Bart Loeys	0
3	Glutamine missense suppressor transfer RNAs inhibit polyglutamine aggregation 2024 ·Molecular Therapy — Nucleic Acids ·(unknown),(unknown),(unknown),(unknown),Aaron Voigt,Tuğçe B. Balcı,Kyle Hoffman,Patrick O’Donoghue	2
4	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
5	Novel findings and expansion of phenotype in a mosaic RASopathy caused by somatic KRAS variants 2021 ·American Journal of Medical Genetics Part A ·(unknown),Renée Perrier,Kyle C. Kurek,Juvianee Estrada‐Veras,Anna Lehman,Stephen Yip,Glenda Hendson,Carol Diamond,Jason W. Pinchot,Jennifer M. Tran,Lisa M. Arkin,Beth A. Drolet,(unknown),(unknown),Tuğçe B. Balcı,Kim M. Keppler‐Noreuil	25
6	Genetic Testing in Children with Epilepsy: Report of a Single-Center Experience 2020 ·Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·(unknown),Natalya Karp,(unknown),Bekim Sadiković,Ping Yang,Tuğçe B. Balcı,Asuri N. Prasad	8
7	Clinical and technical assessment of MedExome vs. NGS panels in patients with suspected genetic disorders in Southwestern Ontario 2020 ·Journal of Human Genetics ·Erfan Aref‐Eshghi,Jennifer Kerkhof,(unknown),Michael Volodarsky,(unknown),(unknown),Maha Saleh,(unknown),Natalya Karp,Chitra Prasad,Tuğçe B. Balcı,Hanxin Lin,(unknown),Victoria Mok Siu,Bekim Sadiković	2
8	Phenotate: crowdsourcing phenotype annotations as exercises in undergraduate classes 2020 ·Genetics in Medicine ·Willie Chang,Pouria Mashouri,Alexander X. Lozano,(unknown),(unknown),Annie Olry,(unknown),Tuğçe B. Balcı,Sarah L. Sawyer,Peter N. Robinson,Ana Rath,Michael Brudno	0
9	BCL11B-related disorder in two canadian children: Expanding the clinical phenotype 2020 ·European Journal of Medical Genetics ·(unknown),Tuğçe B. Balcı,C. Prasad,Joseph Andrews,(unknown),Michael T. Jurkiewicz,(unknown),(unknown),María J. Guillen Sacoto,Natalya Karp	17
10	The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM® 2018 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Taila Hartley,Tuğçe B. Balcı,(unknown),Alison Eaton,(unknown),David A. Dyment,Kym M. Boycott	17
11	Broad spectrum of neuropsychiatric phenotypes associated with white matter disease in PTEN hamartoma tumor syndrome 2017 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Tuğçe B. Balcı,Jorge Dávila,(unknown),Addo Boafo,Erick Sell,Julie Richer,Sarah M. Nikkel,Christine M. Armour,Eva Tomiak,Matthew A. Lines,Sarah L. Sawyer	28
12	Effect of Hereditary Hemochromatosis Gene H63D and C282Y Mutations on Iron Overload in Sickle Cell Disease Patients 2016 ·Turkish Journal of Hematology ·Yunus Kasım Terzi,Tuğçe B. Balcı,Can Boğa,Zafer Koç,Zerrin Yılmaz,Hakan Özdoğu,Sema Karakuş,Feride İffet Şahin	7
13	Detection of α-Thalassemia by Using Multiplex Ligation-Dependent Probe Amplification as an Additional Method for Rare Mutations in Southern Turkey 2015 ·Indian Journal of Hematology and Blood Transfusion ·Özge Özalp Yüreğir,(unknown),(unknown),(unknown),(unknown),(unknown),Tuğçe B. Balcı	5
14	Brain malformations in a patient with deletion 2p16.1: A refinement of the phenotype to BCL11A 2015 ·European Journal of Medical Genetics ·Tuğçe B. Balcı,Sarah L. Sawyer,Jorge Dávila,Peter Humphreys,David A. Dyment	25
15	BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations 2015 ·Journal of Clinical Investigation ·Anindita Basak,Miroslava Hančárová,Jacob C. Ulirsch,Tuğçe B. Balcı,Marie Trková,(unknown),Markéta Vlčková,Kateřina Mužíková,Jaroslav Čermák,Jan Trka,David A. Dyment,Stuart H. Orkin,Mark J. Daly,Zdeněk Sedláček,Vijay G. Sankaran	115
16	Identification of Promoter Region Methylation Patterns of MGMT , CDKN2A , GSTP1 , and THBS1 Genes in Intracranial Meningioma Patients 2012 ·Genetic Testing and Molecular Biomarkers ·(unknown),Erkan Yurtçu,Tuğçe B. Balcı,Feride İffet Şahin,Salih Gülşen,Nur Altınörs	18
17	Fluorescence in situ hybridization analysis of the hTERC region in acute myeloid leukemia patients 2011 ·SHILAP Revista de lepidopterología ·(unknown),Tuğçe B. Balcı,Zerrin Yılmaz,Feride İffet Şahin	1
18	A Unique Role of GATA1s in Down Syndrome Acute Megakaryocytic Leukemia Biology and Therapy 2011 ·PLoS ONE ·Ana C. Xavier,Holly Edwards,Alan A. Dombkowski,Tuğçe B. Balcı,Jason N. Berman,Graham Dellaire,Chengzhi Xie,Steven Buck,Larry H. Matherly,Yubin Ge,Jeffrey W. Taub	11
19	Using the Zebrafish As a Tool for Modeling Systemic Mastocytosis, 2011 ·Blood ·Tuğçe B. Balcı,(unknown),(unknown),Sahar Da’as,Ian C. Chute,D. Léger,Adolfo A. Ferrando,Stephen M. Lewis,Jason N. Berman	1
20	Complex cytogenetic findings in the bone marrow of a chronic idiopathic myelofibrosis patient 2010 ·Turkish Journal of Hematology ·Tuğçe B. Balcı,Meltem Kurt Yüksel,Zerrin Yılmaz,Feride İffet Şahin	1

About Tuğçe B. Balcı

Tuğçe B. Balcı is a scholar working on Genetics, Genetics and Hematology, having authored 30 papers that have together received 531 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Epigenetics and DNA Methylation (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). The work is most often cited by research in Genetics (98 citations), Cell Biology (131 citations) and Hematology (62 citations). Tuğçe B. Balcı has collaborated with scholars based in Canada, United States and Türkiye. Frequent co-authors include Jason N. Berman, Graham Dellaire, Udo F. Hartwig, Martina Konantz, Maya C. André, Claudia Lengerke, David A. Dyment, Sahar Da’as, Jacob C. Ulirsch and Jan Trka. Their work appears in journals such as Journal of Clinical Investigation, 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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