Őzgür Sancak

717 total citations
7 papers, 437 citations indexed

About

Őzgür Sancak is a scholar working on Oncology, Physiology and Molecular Biology. According to data from OpenAlex, Őzgür Sancak has authored 7 papers receiving a total of 437 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Oncology, 5 papers in Physiology and 1 paper in Molecular Biology. Recurrent topics in Őzgür Sancak's work include Tuberous Sclerosis Complex Research (5 papers), Histiocytic Disorders and Treatments (4 papers) and Polyomavirus and related diseases (3 papers). Őzgür Sancak is often cited by papers focused on Tuberous Sclerosis Complex Research (5 papers), Histiocytic Disorders and Treatments (4 papers) and Polyomavirus and related diseases (3 papers). Őzgür Sancak collaborates with scholars based in Netherlands, United States and Belgium. Őzgür Sancak's co-authors include Miriam Goedbloed, Dicky Halley, Mark Nellist, Anneke Maat‐Kievit, Ans van den Ouweland, Carine Wouters, Peter Elfferich, Bernard A. Zonnenberg, Senno Verhoef and Ans M.W. van den Ouweland and has published in prestigious journals such as Epilepsia, European Journal of Human Genetics and BMC Medical Genetics.

In The Last Decade

Őzgür Sancak

6 papers receiving 432 citations

Peers

Countries citing papers authored by Őzgür Sancak

Since Specialization

Citations

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

Fields of papers citing papers by Őzgür Sancak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Őzgür Sancak

This figure shows the co-authorship network connecting the top 25 collaborators of Őzgür Sancak. A scholar is included among the top collaborators of Őzgür Sancak 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 Őzgür Sancak. Őzgür Sancak is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Functional characterisation of the TSC1–TSC2 complex to assess multiple TSC2 variants identified in single families affected by tuberous sclerosis complex 2008 ·BMC Medical Genetics ·Mark Nellist, Őzgür Sancak, Miriam Goedbloed, (unknown), Marja W. Wessels, (unknown), Marieke J.H. Baars, Charlotte J. Dommering, (unknown), Dicky Halley	16
2	CHOREA-ACANTHOCYTOSIS (ChAc) IN FRENCH CANADIANS:FOUNDER EFFECT, SEIZURE CHARACTERISATIONAND GENOTYPE-PHENOTYPE CORRELATIONS 2006 ·E. Andermann, Anna Jansen, Őzgür Sancak, Donato D’Agostino, AmanPreet Badhwar, Penelope Roberts, R. D. Wilkinson, Denis Melanson, Donatella Tampieri, Anneke Maat‐Kievit, (unknown), A M van den Ouweland, Mark Nellist, Massimo Pandolfo, Katherine B. Sims, Elizabeth A. Thiele, François Dubeau, Frédérick Andermann, David J. Kwiatkowski, Dicky Halley	0
3	Large Deletion at the TSC1 Locus in a Family with Tuberous Sclerosis Complex 2005 ·Genetic Testing ·Mark Nellist, Őzgür Sancak, Miriam Goedbloed, (unknown), Anneke Maat‐Kievit, Dick Lindhout, Bert H.J. Eussen, Annelies de Klein, Dicky Halley, A.M.W. van den Ouweland	8
4	Mild Epilepsy Phenotype in TSC2 Patients with Codon 905 Mutations 2005 ·Epilepsia ·Anna Jansen, Őzgür Sancak, Daniela D’Agostino, AmanPreet Badhwar, Penelope Roberts, G. Gobbi, (unknown), Denis Melanson, (unknown), Madeleine Gans, A M van den Ouweland, Mark Nellist, Massimo Pandolfo, Katherine B. Sims, Elizabeth A. Thiele, Frédérick Andermann, François Dubeau, David J. Kwiatkowski, Dicky Halley, E. Andermann	2
5	Mutational analysis of the TSC1 and TSC2 genes in a diagnostic setting: genotype – phenotype correlations and comparison of diagnostic DNA techniques in Tuberous Sclerosis Complex 2005 ·European Journal of Human Genetics ·Őzgür Sancak, Mark Nellist, Miriam Goedbloed, Peter Elfferich, Carine Wouters, Anneke Maat‐Kievit, Bernard A. Zonnenberg, Senno Verhoef, Dicky Halley, Ans van den Ouweland	344
6	Tuberous Sclerosis Complex: mutations, functions and phenotypes 2005 ·RePub (Erasmus University Rotterdam) ·Őzgür Sancak	2
7	Distinct effects of single amino-acid changes to tuberin on the function of the tuberin–hamartin complex 2004 ·European Journal of Human Genetics ·Mark Nellist, Őzgür Sancak, Miriam Goedbloed, Christan F. Rohé, (unknown), Karin Mayer, (unknown), Ans M.W. van den Ouweland, Dicky Halley	65

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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