Asude Alpman

471 total citations
14 papers, 365 citations indexed

About

Asude Alpman is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Asude Alpman has authored 14 papers receiving a total of 365 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Oncology and 3 papers in Genetics. Recurrent topics in Asude Alpman's work include Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Epilepsy research and treatment (2 papers). Asude Alpman is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Epilepsy research and treatment (2 papers). Asude Alpman collaborates with scholars based in Türkiye, United States and Sweden. Asude Alpman's co-authors include Ferda Özkınay, Martin Schalling, Sarenur Gökben, Hasan Tekgül, Jens Treutlein, Ping Chen, Leena Peltonen, Mark Lathrop, A. Koch and Pia Soronen and has published in prestigious journals such as Neurology, Developmental Medicine & Child Neurology and Annals of Medicine.

In The Last Decade

Asude Alpman

14 papers receiving 356 citations

Peers

Countries citing papers authored by Asude Alpman

Since Specialization

Citations

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

Fields of papers citing papers by Asude Alpman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Asude Alpman

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

All Works

Sort: Min cites: Since: Top N: Style:

14 of 14 papers shown

#	Work	Indexed citations
1	Progressive Multifocal Leukoencephalopathy Associated with Idiopathic CD4+ Lymphocytopenia in a Patient with Heterozygous STAT4 Mutation (4414) 2020 ·Neurology ·(unknown), (unknown), Tuncay Gündüz, (unknown), (unknown), Asude Alpman, Ayça Aykut, Semra Demir, Figen Söylemezoğlu, Murat Kürtüncü, Mefkûre Eraksoy	1
2	The Effect of HFE Polymorphisms on Cardiac Iron Overload in Patients with Beta-Thalassemia Major 2013 ·Pediatric Hematology and Oncology ·(unknown), Yeşim Oymak, Timur Meşe, (unknown), Selen Bayraktaroğlu, Asude Alpman, Ferda Özkınay, Yeşim Aydınok, Canan Vergin	5
3	Homozygous mutation of CRLF-1 gene in a Turkish newborn with Crisponi syndrome 2011 ·Clinical Dysmorphology ·(unknown), (unknown), (unknown), (unknown), Ali Kanık, Sümer Sütçüoğlu, Hüseyin Önay, Asude Alpman, Ferda Özkınay, Esra Arun Özer	8
4	Multidrug Resistance 1 (MDR1) Gene Polymorphisms in Childhood Drug-Resistant Epilepsy 2010 ·Journal of Child Neurology ·Asude Alpman, Ferda Özkınay, Hasan Tekgül, Sarenur Gökben, Sacide Pehlıvan, Martin Schalling, Cihangir Özkınay	26
5	Evaluation of the SMN and NAIP Genes in a Family: Homozygous Deletion of the SMN2 Gene in the Fetus and Outcome of the Pregnancy 2009 ·Genetic Testing and Molecular Biomarkers ·Özgür Çoğulu, Burak Durmaz, Sacide Pehlıvan, Asude Alpman, Ferda Özkınay	2
6	The Evaluation of the Referral Reasons of Patients at a Tertiary Pediatric Genetic Center in Izmir, Turkey 2009 ·Genetic Testing and Molecular Biomarkers ·Burak Durmaz, Asude Alpman, (unknown), Mehmet Akgül, (unknown), Özgür Kırbıyık, Özgür Çoğulu, Ferda Özkınay	1
7	Febrile Seizures: Interleukin 1β and Interleukin-1 Receptor Antagonist Polymorphisms 2009 ·Pediatric Neurology ·Gül Serdaroğlu, Asude Alpman, Ayşe Tosun, Sacide Pehlıvan, Ferda Özkınay, Hasan Tekgül, Sarenur Gökben	31
8	Prenatally Diagnosed Turner Syndrome and Cystic Hygroma: Incidence and Reasons for Referrals 2008 ·Fetal Diagnosis and Therapy ·Asude Alpman, Özgür Çoğulu, (unknown), (unknown), Burak Durmaz, Emin Karaca, Sermet Sağol, Cihangir Özkınay, Ferda Özkınay	26
9	Chronic myelogenous leukemia exhibiting trisomy 14 due to a Robertsonian translocation with philadelphia chromosome 2008 ·Acta Oncologica ·Burak Durmaz, Emin Karaca, Filiz Vural, Özgür Çoğulu, Asude Alpman, Murat Tombuloğlu, Ferda Özkınay	1
10	Association of interleukin-1beta and interleukin-1 receptor antagonist gene polymorphisms in Turkish children with atopic asthma 2008 ·Allergy and Asthma Proceedings ·Dost Zeyrek, Esen Demir, Asude Alpman, Ferda Özkınay, Figen Gülen, Remziye Tanaç	23
11	Congenital supratentorial cystic hemangioblastoma 2007 ·Journal of Neurosurgery Pediatrics ·Hakan Karabağlı, Pınar Karabağli, Asude Alpman, Burak Durmaz	16
12	Three circadian clock genes Per2, Arntl, and Npas2 contribute to winter depression 2007 ·Annals of Medicine ·Timo Partonen, Jens Treutlein, Asude Alpman, Josef Frank, Carolina Johansson, Martin Depner, (unknown), Marcella Rietschel, Stefan Wellek, Pia Soronen, Tiina Paunio, A. Koch, Ping Chen, Mark Lathrop, Rolf Adolfsson, (unknown), Siegfried Kasper, Martin Schalling, Leena Peltonen, Günter Schumann	209
13	Ring chromosome 20 syndrome with intractable epilepsy 2007 ·Developmental Medicine & Child Neurology ·Asude Alpman, Gül Serdaroğlu, Özgür Çoğulu, Hasan Tekgül, Sarenur Gökben, Ferda Özkınay	3
14	Ring chromosome 20 syndrome with intractable epilepsy 2005 ·Developmental Medicine & Child Neurology ·Asude Alpman, Gül Serdaroğlu, Özgür Çoğulu, Hasan Tekgül, Sarenur Gökben, Ferda Özkınay	13

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.

Explore authors with similar magnitude of impact