Beril Talim

7.8k total citations · 1 hit paper
138 papers, 4.0k citations indexed

About

Beril Talim is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Beril Talim has authored 138 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Molecular Biology, 35 papers in Surgery and 18 papers in Genetics. Recurrent topics in Beril Talim's work include Muscle Physiology and Disorders (56 papers), Mitochondrial Function and Pathology (18 papers) and Neurogenetic and Muscular Disorders Research (18 papers). Beril Talim is often cited by papers focused on Muscle Physiology and Disorders (56 papers), Mitochondrial Function and Pathology (18 papers) and Neurogenetic and Muscular Disorders Research (18 papers). Beril Talim collaborates with scholars based in Türkiye, United Kingdom and Germany. Beril Talim's co-authors include Haluk Topaloğlu, Gülsev Kale, Göknur Haliloğlu, Luciano Merlini, Thomas Voit, Pervin Dinçer, Tatsushi Toda, Ralf Herrmann, Hiroshi Manya and Hiroki Kano and has published in prestigious journals such as New England Journal of Medicine, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Beril Talim

131 papers receiving 3.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Muscular Dystrophy and Neuronal Migration Disorder Caused by Mutations in a Glycosyltransferase, POMGnT1

2001 536 citations Ralf Herrmann, Beril Talim et al. profile →

Peers

Countries citing papers authored by Beril Talim

Since Specialization

Citations

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

Fields of papers citing papers by Beril Talim

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Beril Talim

This figure shows the co-authorship network connecting the top 25 collaborators of Beril Talim. A scholar is included among the top collaborators of Beril Talim 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 Beril Talim. Beril Talim 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	Neurogenic arthrogryposis, hypotonia, dysmorphic features plus malformation of cortical development further expands the ARL6IP1 loss-of-function phenotype 2025 ·Neuromuscular Disorders ·Göknur Haliloğlu, (unknown), (unknown), Ikeoluwa Osei‐Owusu, Lynn Pais, (unknown), Beril Talim, Rahşan Göçmen, Serdar Ceylaner, Carsten G. Bönnemann	1
2	A Founder Allele in SGCG Combining Missense Variant and Multi‐Exon Duplication in Turkish Patients With Sarcoglycanopathy 2025 ·Clinical Genetics ·(unknown), (unknown), Hasan Hüseyin Kazan, (unknown), (unknown), Beril Talim, Deniz Yüksel, (unknown)	0
3	Nemaline rod myopathy treated with L-tyrosine to relieve symptoms in a neonate 2019 ·Archivos Argentinos de Pediatria ·(unknown), Mehmet Yekta Öncel, (unknown), Nilüfer Okur, Beril Talim, Şerife Suna Oğuz, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	0
4	Do not Miss Rare and Treatable Cause of Early-Onset Hemolytic Uremic Syndrome: Cobalamin C Deficiency 2019 ·The Nephron journals/Nephron journals ·Rezan Topaloğlu, (unknown), Bora Gülhan, (unknown), Beril Talim, Turgay Coşkun	5
5	Bi-allelic mutations in MYL1 cause a severe congenital myopathy 2018 ·Human Molecular Genetics ·Gianina Ravenscroft, Irina Zaharieva, Carlo Augusto Bortolotti, Matteo Lambrughi, (unknown), Marco Borsari, Caroline A. Sewry, Rahul Phadke, Göknur Haliloğlu, Royston Ong, Hayley Goullée, Tamieka Whyte, Adnan Manzur, Beril Talim, (unknown), Daniel P. S. Osborn, Alistair R. R. Forrest, Nigel G. Laing, Francesco Muntoni	29
6	Unusual splenic hemangioma of a pediatric patient: hypointense on T2-weighted image 2014 ·Clinical Imaging ·H. Nursun Özcan, Berna Oğuz, Beril Talim, Saniye Ekinci, Mithat Haliloğlu	2
7	190th ENMC international workshop: Spinal muscular atrophy with respiratory distress/distal spinal muscular atrophy type 1 2013 ·Neuromuscular Disorders ·W. Ludo van der Pol, Beril Talim, Matthew Pitt, Katja von Au	6
8	Early corticosteroid treatment in 4 duchenne muscular dystrophy patients: 14‐year follow‐up 2012 ·Muscle & Nerve ·Luciano Merlini, Monia Gennari, Elisabetta Malaspina, I Cecconi, Annarita Armaroli, S Gnudi, Beril Talim, Alessandra Ferlini, Alessandro Cicognani, Emilio Franzonı	88
9	BRIEF REPORT A Dystroglycan Mutation Associated with Limb-Girdle Muscular Dystrophy 2011 ·UCL Discovery (University College London) ·Yuko Hara, Burcu Balcı-Hayta, Takako Yoshida‐Moriguchi, Motoi Kanagawa, (unknown), Hülya Gündeşli, Tobias Willer, (unknown), Ross Crawford, Steven J. Burden, Séverine Kunz, (unknown), Alessio Accardi, Beril Talim, Francesco Muntoni, Haluk Topaloğlu, Pervin Dinçer, Kevin P. Campbell	0
10	A Dystroglycan Mutation Associated with Limb-Girdle Muscular Dystrophy 2011 ·New England Journal of Medicine ·Yuji Hara, Burcu Balcı-Hayta, Takako Yoshida‐Moriguchi, Motoi Kanagawa, Daniel Beltrán-Valero de Bernabé, Hülya Gündeşli, Tobias Willer, Jakob S. Satz, Robert W. Crawford, Steven J. Burden, Stefan Kunz, Michael B. A. Oldstone, Alessio Accardi, Beril Talim, Francesco Muntoni, Haluk Topaloğlu, Pervin Dinçer, Kevin P. Campbell	178
11	Mutation in Exon 1f of PLEC, Leading to Disruption of Plectin Isoform 1f, Causes Autosomal-Recessive Limb-Girdle Muscular Dystrophy 2010 ·The American Journal of Human Genetics ·Hülya Gündeşli, Beril Talim, Petek Korkusuz, Burcu Balcı-Hayta, Sebahattin Çirak, Nurten Akarsu, Haluk Topaloğlu, Pervin Dinçer	79
12	Akut Respiratuvar Distres Sendromu 2009 ·Beril Talim	1
13	Does Defective Apoptosis Play A Role in Cystic Fibrosis Lung Disease? 2009 ·Archives of Medical Research ·Ebru Yalçın, Beril Talim, Uğur Özçelik, Deni̇z Doğru, Nazan Çobanoğlu, Sevgi Pekcan, Nural Ki̇per	9
14	G.P.2.15 EUROSMART: European Spinal Muscular Atrophy Randomised Placebo-Controlled Trial of acetyl-L-carnitine in spinal muscular atrophy 2007 ·Neuromuscular Disorders ·Luciano Merlini, (unknown), Christian Dohna‐Schwake, (unknown), (unknown), Maria Jędrzejowska, Mario Luppi, Yehuda Shapira, (unknown), Eduardo F. Tizzano, Haluk Topaloğlu, Thomas Voit, Beril Talim	2
15	C.P.2.12 Congenital muscular dystrophy with mental retardation, dilated cardiomyopathy and abnormally located mitochondria 2007 ·Neuromuscular Disorders ·Beril Talim, (unknown), Zühal Akçören, Meral Topçu, Dursun Alehan, (unknown), Haluk Topaloğlu	1
16	G.P.1.02 10 years follow-up of early corticosteroid treatment of Duchenne muscular dystrophy 2007 ·Neuromuscular Disorders ·Luciano Merlini, Elisabetta Malaspina, (unknown), Alessandro Cicognani, Emilio Franzonı, Beril Talim	0
17	Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit 2006 ·The American Journal of Human Genetics ·Katrin Hoffmann, Juliane Müller, Sigmar Stricker, André Mégarbané, Anna Rajab, Tom H. Lindner, Monika Cohen, Éliane Chouery, (unknown), Ismat Ghanem, Valérie Delague, Eugen Boltshauser, Beril Talim, Rita Horváth, Peter N. Robinson, Hanns Lochmüller, Christoph Hübner, Stefan Mundlos	100
18	125th ENMC International Workshop: Neuromuscular Disorders in the Roma (Gypsy) Population, 23–25 April 2004, Naarden, The Netherlands 2004 ·Neuromuscular Disorders ·Luba Kalaydjieva, Hanns Lochmüller, Ivailo Tournev, Frank Baas, Judit Béres, J. Colomer, Velina Guergueltcheva, Ralf Herrmann, Veronika Karcagi, R. H. M. King, Toshiyuki Miyata, Andrea Müllner-Eidenböck, Tomohiko Okuda, Vedrana Milić Rašić, (unknown), Beril Talim, Juan J. Vílchez, Maggie C. Walter, Andoni Urtizberea, Luciano Merlini	22
19	Genetic identity of Marinesco–Sjogren/myoglobinuria and CCFDN syndromes 2002 ·Neurology ·Luciano Merlini, Rebecca Gooding, Hanns Lochmüller, Wolfgang Müller‐Felber, Maggie C. Walter, Dora Angelicheva, Beril Talim, Joachim Hallmayer, Luba Kalaydjieva	25
20	Pyogenic Granuloma with Multiple Dissemination in a Burn Lesion 1997 ·Pediatric Dermatology ·Mehmet Ceyhan, Güliz Erdem, Esin Kotiloğlu, Gülsev Kale, Beril Talim, G Kanra, (unknown)	24

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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