Yasemin Alanay

7.3k total citations
108 papers, 2.1k citations indexed

About

Yasemin Alanay is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Yasemin Alanay has authored 108 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Genetics, 45 papers in Molecular Biology and 17 papers in Surgery. Recurrent topics in Yasemin Alanay's work include Connective tissue disorders research (25 papers), Genomic variations and chromosomal abnormalities (14 papers) and Neurogenetic and Muscular Disorders Research (9 papers). Yasemin Alanay is often cited by papers focused on Connective tissue disorders research (25 papers), Genomic variations and chromosomal abnormalities (14 papers) and Neurogenetic and Muscular Disorders Research (9 papers). Yasemin Alanay collaborates with scholars based in Türkiye, United States and Germany. Yasemin Alanay's co-authors include Koray Boduroğlu, Ergül Tunçbılek, Ralph S. Lachman, Andrea Superti‐Furga, Mehmet Alikaşifoğlu, Deborah Krakow, David L. Rimoin, Pelin Özlem Şimşek‐Kiper, Dilek Aktaş and Luisa Bonafé and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Spine.

In The Last Decade

Yasemin Alanay

103 papers receiving 2.0k citations

Peers

Countries citing papers authored by Yasemin Alanay

Since Specialization

Citations

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

Fields of papers citing papers by Yasemin Alanay

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yasemin Alanay

This figure shows the co-authorship network connecting the top 25 collaborators of Yasemin Alanay. A scholar is included among the top collaborators of Yasemin Alanay 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 Yasemin Alanay. Yasemin Alanay 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	A new line method; A direct test in spinal muscular atrophy screening for DBS 2023 ·Molecular Genetics & Genomic Medicine ·Ayhan Kubar, Şehime Gülsün Temel, Serdar Beken, (unknown), Özden Hatırnaz Ng, Ayşe Korkmaz, Yasemin Alanay, Uğur Özbek, (unknown), Mahmut Çerkez Ergören, (unknown), (unknown), (unknown)	1
2	DNAJC21‐related thrombocytopenia in a young adult female 2023 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·(unknown), Özlem Akgün Doğan, (unknown), Mahmut Orhun Çamurdan, (unknown), Yasemin Alanay	0
3	Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defects 2023 ·Human Genetics and Genomics Advances ·Jessica X. Chong, Matthew C. Childers, Colby T. Marvin, (unknown), Hernán Gonorazky, Lili‐Naz Hazrati, James J. Dowling, (unknown), Yasemin Alanay, Yolanda Ber, Miguel Ángel Marín Gabriel, Arthur S. Aylsworth, Kati J. Buckingham, Kathryn M. Shively, (unknown), (unknown), Michael Regnier, Michael J. Bamshad	9
4	Spondyloepimetaphyseal dysplasia EXTL3‐deficient type: Long‐term follow‐up and review of the literature 2021 ·American Journal of Medical Genetics Part A ·(unknown), Ekim Z. Taşkıran, Pelin Özlem Şimşek‐Kiper, Eda Ütine, Yasemin Alanay, Uğur Özçelik, Koray Boduroğlu	5
5	Investigation of Genetic Causes in a Developmental Disorder: Oculoauriculovertebral Spectrum 2021 ·The Cleft Palate-Craniofacial Journal ·(unknown), Can Koşukçu, (unknown), (unknown), Ekim Z. Taşkıran, Pelin Özlem Şimşek‐Kiper, Gülen Eda Ütine, Yasemin Alanay, Koray Boduroğlu, Mehmet Alikaşifoğlu	4
6	COVID-19 Küresel Salgınında Tıp Eğitimi Nasıl Etkilendi? Acıbadem Üniversitesi Tıp Fakültesi Deneyimi 2021 ·Tıp Eğitimi Dünyası ·Nadi Bakırcı, (unknown), (unknown), Güldal Güleç Süyen, Yasemin Alanay	1
7	The process of how mothers with down’s syndrome children learn about the diagnosis: A qualitative research 2020 ·The Annals of Clinical and Analytical Medicine ·(unknown), (unknown), Yasemin Alanay, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	1
8	Clinical and Molecular Characterization of Fanconi Anemia Patients in Turkey 2020 ·Molecular Syndromology ·Güven Toksoy, (unknown), (unknown), Şahin Avcı, (unknown), Nilay Güneş, Umut Altunoğlu, Yasemin Alanay, Seher Başaran, (unknown), Birsen Karaman, Tiraje Çelkan, Hilmi Apak, Hülya Kayserili, Beyhan Tüysüz, Zehra Oya Uyguner	6
9	A possible founder mutation in FZD6 gene in a Turkish family with autosomal recessive nail dysplasia 2019 ·BMC Medical Genetics ·Ceren Saygı, Yasemin Alanay, Osman Uğur Sezerman, (unknown), Nesrin Özören	8
10	A Chaperone Complex Formed by HSP47, FKBP65, and BiP Modulates Telopeptide Lysyl Hydroxylation of Type I Procollagen 2017 ·Journal of Bone and Mineral Research ·Iván Durán, Jorge Martı́n, Mary Ann Weis, Pavel Krejčı́, Peter Koník, Bing Li, Yasemin Alanay, Caressa Lietman, Brendan Lee, David R. Eyre, Daniel H. Cohn, Deborah Krakow	56
11	Dental Findings and Mutational Analysis of a Case with Ehlers-Danlos Syndrome 2017 ·Sema S. Hakkı, Dilek Aktaş, Yasemin Alanay, Mustafa Cihat Avunduk, Erdoğan E. Hakkı	2
12	Is 1p36 deletion associated with anterior body wall defects? 2016 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), Latif Abbasoğlu, Yasemin Alanay	3
13	Expanding the clinical and mutational spectrum of the Ehlers–Danlos syndrome, dermatosparaxis type 2016 ·Genetics in Medicine ·Tim Van Damme, Alain Colige, Delfien Syx, Cecilia Giunta, Uschi Lindert, Marianne Rohrbach, Omid Aryani, Yasemin Alanay, Pelin Özlem Şimşek‐Kiper, Hester Y. Kroes, Koenraad Devriendt, Marc Thiry, Sofie Symoens, Anne De Paepe, Fransiska Malfait	34
14	Experience of a skeletal dysplasia registry in Turkey: A five‐years retrospective analysis 2015 ·American Journal of Medical Genetics Part A ·(unknown), Pelin Özlem Şimşek‐Kiper, Gülen Eda Ütine, Koray Boduroğlu, Yasemin Alanay	12
15	Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features 2014 ·Orphanet Journal of Rare Diseases ·Ahmet Arman, Abdullah Bereket, Ajda Çoker Gürkan, Pelin Özlem Şimşek‐Kiper, Tülay Güran, Behzat Özkan, Zeynep Atay, Teoman Akçay, Belma Haliloğlu, Koray Boduroğlu, Yasemin Alanay, Serap Turan	34
16	A Review of the Principles of Radiological Assessment of Skeletal Dysplasias 2011 ·Journal of Clinical Research in Pediatric Endocrinology ·Yasemin Alanay, Ralph S. Lachman	40
17	Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting: Expanding the Spectrum of Autosomal-Recessive ALX-Related Frontonasal Dysplasia 2010 ·The American Journal of Human Genetics ·Elif Uz, Yasemin Alanay, Dilek Aktaş, İbrahim Vargel, Şafak Güçer, Gökhan Tunçbįlek, Ferdinand von Eggeling, Engin Yılmaz, Özgür Deren, Nicole Posorski, Hi̇lal Özdağ, Thomas Liehr, Sevim Balcı, Mehmet Alikaşifoğlu, Bernd Wollnik, Nurten Akarsu	101
18	Homozygous Inactivating Mutations in the NKX3-2 Gene Result in Spondylo-Megaepiphyseal-Metaphyseal Dysplasia 2009 ·The American Journal of Human Genetics ·Jan Hellemans, Marleen Simon, Annelies Dheedene, Yasemin Alanay, Ercan Mıhçı, (unknown), Abdelaziz Sefiani, Yolande van Bever, M. Meradji, Andrea Superti‐Furga, Geert Mortier	28
19	TBX15 Mutations Cause Craniofacial Dysmorphism, Hypoplasia of Scapula and Pelvis, and Short Stature in Cousin Syndrome 2008 ·The American Journal of Human Genetics ·Ekkehart Lausch, Pia Hermanns, Henner F. Farin, Yasemin Alanay, Sheila Unger, Sarah M. Nikkel, (unknown), Gerd Scherer, Jürgen W. Spranger, Bernhard Zabel, Andreas Kispert, Andrea Superti‐Furga	46
20	The Skeletal Dysplasias 2007 ·Annals of the New York Academy of Sciences ·David L. Rimoin, Daniel H. Cohn, Deborah Krakow, William R. Wilcox, Ralph S. Lachman, Yasemin Alanay	47

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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