Güven Lüleci

2.4k total citations
110 papers, 1.7k citations indexed

About

Güven Lüleci is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Güven Lüleci has authored 110 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Genetics, 38 papers in Molecular Biology and 25 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Güven Lüleci's work include Genomic variations and chromosomal abnormalities (30 papers), Prenatal Screening and Diagnostics (20 papers) and Hemoglobinopathies and Related Disorders (14 papers). Güven Lüleci is often cited by papers focused on Genomic variations and chromosomal abnormalities (30 papers), Prenatal Screening and Diagnostics (20 papers) and Hemoglobinopathies and Related Disorders (14 papers). Güven Lüleci collaborates with scholars based in Türkiye, United States and Switzerland. Güven Lüleci's co-authors include Salih Şanlıoğlu, Umit A. Kayisli, Aydın Arıcı, Mehmet Baykara, Ozlem Guzeloglu‐Kayisli, I Keser, Zafer Çetin, Özgül M. Alper, Türker Bilgen and Ahter Dilşad Şanlioğlu and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Güven Lüleci

108 papers receiving 1.6k citations

Peers

Countries citing papers authored by Güven Lüleci

Since Specialization

Citations

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

Fields of papers citing papers by Güven Lüleci

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Güven Lüleci

This figure shows the co-authorship network connecting the top 25 collaborators of Güven Lüleci. A scholar is included among the top collaborators of Güven Lüleci 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 Güven Lüleci. Güven Lüleci 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	Mitochondrial ATPase Subunit 6 and Cytochrome B Gene Variations in Obese Turkish Children 2014 ·Journal of Clinical Research in Pediatric Endocrinology ·(unknown), Doğa Türkkahraman, Anıl Aktaş Samur, Güven Lüleci, Sema Akçurin, Özgül M. Alper	6
2	Mixed gonadal dysgenesis in a patient with de novo tas(Y;19)(p11.3;q13.4) and 45,X mosaicism 2013 ·European Journal of Pediatrics ·Zafer Çetin, Mesut Parlak, (unknown), Güngör Karagüzel, Güven Lüleci, İffet Bircan, (unknown)	1
3	Aberrations of Chromosomes 9 and 22 in Acute Lymphoblastic Leukemia Cases Detected by ES-Fluorescence In Situ Hybridization 2012 ·Genetic Testing and Molecular Biomarkers ·Zafer Çetin, (unknown), Ìhsan Karadoǧan, Alphan Küpesiz, Ayşen Timurağaoğlu, Ozan Salim, (unknown), (unknown), (unknown), Volkan Hazar, M. Akif Yeşilipek, Levent Ündar, Güven Lüleci, (unknown)	1
4	A 5q12.1–5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement 2012 ·Gene ·Zafer Çetin, (unknown), (unknown), Ercan Mıhçı, (unknown), Güven Lüleci	9
5	Absence of the SLC22A12 gene mutation in Turkish population with primary gout disease 2012 ·Rheumatology International ·(unknown), Zafer Çetin, (unknown), Halide Akbaş, (unknown), Güven Lüleci	2
6	Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1) 2011 ·SHILAP Revista de lepidopterología ·Zafer Çetin, İnanç Mendilcioğlu, (unknown), (unknown), Birsen Karaman, Güven Lüleci	2
7	Complete gonadal dysgenesis 46,XY (Swyer syndrome) in two sisters and their mother's maternal aunt with a female phenotype 2010 ·Fertility and Sterility ·Gülseren Bağcı, Atıl Bişgin, (unknown), (unknown), Güven Lüleci	10
8	The frequency and medical effects of consanguineous marriages in Antalya, Turkey 2008 ·Hereditas ·(unknown), Necati Dedeoğlu, Güven Lüleci	8
9	Combination of Hb Knossos [Cod 27 (G-T)] and IVSII-745 (C-G) in a Turkish Patient with Beta-Thalassemia Major 2007 ·Genetic Testing ·İbrahim Keser, (unknown), (unknown), Akif Yeşilipek, Güven Lüleci	4
10	Prenatal Diagnosis of b-Thalassemia in the Antalya Province 2005 ·TURKISH JOURNAL OF MEDICAL SCIENCES ·İbrahim Keser, (unknown), (unknown), (unknown), İnanç Mendilcioğlu, Mehmet Şımşek, Gülseren Bağcı, (unknown), Güven Lüleci	4
11	Identification of a Novel Frameshift Mutation [Codon 3 (+T)] in a Turkish Patient with \beta-Thalassemia Intermedia 2005 ·TURKISH JOURNAL OF MEDICAL SCIENCES ·(unknown), İbrahim Keser, Duran Canatan, Ahter Dilşad Şanlioğlu, Osman Nidai Özeş, Güven Lüleci	2
12	Mutation Analysis By The Use of Temporal Temperature Gradient Gel Electrophoresis 2005 ·TURKISH JOURNAL OF MEDICAL SCIENCES ·Özgül M. Alper, Güven Lüleci, Lee‐Jun C. Wong	1
13	KRIT1/Cerebral Cavernous Malformation 1 Protein Localizes to Vascular Endothelium, Astrocytes, and Pyramidal Cells of the Adult Human Cerebral Cortex 2004 ·Neurosurgery ·Ozlem Guzeloglu‐Kayisli, (unknown), Jennifer Voorhees, Güven Lüleci, Richard P. Lifton, Murat Günel	48
14	Consanguineous marriages in the province of Antalya, Turkey 2003 ·Annales de Génétique ·Özgül M. Alper, Hakan Erengin, (unknown), Türker Bilgen, Zehra Güven Çetin, Necati Dedeoğlu, Güven Lüleci	57
15	Germline mutations in theBRCA1andBRCA2genes in Turkish breast/ovarian cancer patients 2003 ·Human Mutation ·(unknown), Güven Lüleci, Tayfun Özçelık, Tahsin Çolak, Hagit Schayek, M Akaydın, Eitan Friedman	18
16	Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome 2002 ·Nature Genetics ·Kirk Mykytyn, Darryl Nishimura, Charles Searby, (unknown), (unknown), John S. Beck, Terry A. Braun, Luan M. Streb, Alberto S. Cornier, Gerald F. Cox, Anne B. Fulton, Rivka Carmi, Güven Lüleci, Settara C. Chandrasekharappa, Francis S. Collins, Samuel G. Jacobson, John R. Heckenlively, Richard G. Weleber, Edwin M. Stone, Val C. Sheffield	258
17	Telomere‐specific fluorescence in situ hybridization analysis of couples with five or more recurrent miscarriages 2002 ·Clinical Genetics ·(unknown), (unknown), Mehmet Şımşek, Gürkan Zorlu, (unknown), Güven Lüleci	10
18	Hb ANTALYA [CODONS 3–5 (Leu-Thr-Pro → Ser-Asp-Ser)]: A NEW UNSTABLE VARIANT LEADING TO CHRONIC MICROCYTIC ANEMIA AND HIGH Hb A₂ 2001 ·Hemoglobin ·İbrahim Keser, (unknown), Akif Yeşilipek, Osman N. Özeş, Güven Lüleci	8
19	Cytogenetic studies among mentally retarded children attending to special classes of mebaram in antalya province 1998 ·Marmara medical journal ·I Keser, Güven Lüleci, (unknown)	2
20	Monosomy 7 Myelodysplasia in Childhood 1994 ·Acta Haematologica ·Akif Yeşilipek, Güven Lüleci, (unknown), (unknown), Olcay Yeğin	1

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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