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, Volker Straub and Tamao Endo 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 sort by overperformance

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 →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Beril Talim	3.0k	609	580	492	487	138	4.0k
Reginald E. Bittner	2.1k 0.7×	657 1.1×	417 0.7×	509 1.0×	411 0.8×	82	3.5k
Patrizia Sabatelli	4.3k 1.4×	912 1.5×	478 0.8×	553 1.1×	539 1.1×	147	5.6k
Lucía Morandi	3.7k 1.2×	613 1.0×	754 1.3×	786 1.6×	835 1.7×	143	5.2k
France Leturcq	3.4k 1.1×	547 0.9×	890 1.5×	947 1.9×	639 1.3×	130	4.0k
Yoshihide Sunada	3.9k 1.3×	1.0k 1.7×	973 1.7×	630 1.3×	371 0.8×	144	5.2k
Lise K. Sorensen	2.2k 0.7×	562 0.9×	938 1.6×	266 0.5×	359 0.7×	28	4.1k
Helge Amthor	2.8k 0.9×	547 0.9×	204 0.4×	345 0.7×	394 0.8×	57	3.3k
Daniel E. Michele	3.5k 1.2×	765 1.3×	625 1.1×	1.1k 2.3×	219 0.4×	69	4.6k
Eduard Gallardo	2.2k 0.7×	435 0.7×	1.1k 2.0×	363 0.7×	407 0.8×	133	4.6k
Johanna Andræ	2.0k 0.7×	344 0.6×	348 0.6×	212 0.4×	389 0.8×	35	4.4k

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

Haliloğlu, Göknur, Ikeoluwa Osei‐Owusu, Lynn Pais, et al.. (2025). Neurogenic arthrogryposis, hypotonia, dysmorphic features plus malformation of cortical development further expands the ARL6IP1 loss-of-function phenotype. Neuromuscular Disorders. 48. 105312–105312. 1 indexed citations

Kazan, Hasan Hüseyin, et al.. (2025). A Founder Allele in SGCG Combining Missense Variant and Multi‐Exon Duplication in Turkish Patients With Sarcoglycanopathy. Clinical Genetics. 109(2). 294–304.

Öncel, Mehmet Yekta, et al.. (2019). Nemaline rod myopathy treated with L-tyrosine to relieve symptoms in a neonate. Archivos Argentinos de Pediatria. 117(4).

Topaloğlu, Rezan, et al.. (2019). Do not Miss Rare and Treatable Cause of Early-Onset Hemolytic Uremic Syndrome: Cobalamin C Deficiency. The Nephron journals/Nephron journals. 142(3). 258–263. 5 indexed citations

Ravenscroft, Gianina, Irina Zaharieva, Carlo Augusto Bortolotti, et al.. (2018). Bi-allelic mutations in MYL1 cause a severe congenital myopathy. Human Molecular Genetics. 27(24). 4263–4272. 29 indexed citations

Ceyhan‐Birsoy, Ozge, Beril Talim, Lindsay C. Swanson, et al.. (2015). Whole Exome Sequencing Reveals DYSF, FKTN, and ISPD Mutations in Congenital Muscular Dystrophy Without Brain or Eye Involvement. Journal of Neuromuscular Diseases. 2(1). 87–92. 10 indexed citations

Agrawal, Pankaj B., Christopher R. Pierson, Mugdha Joshi, et al.. (2014). SPEG Interacts with Myotubularin, and Its Deficiency Causes Centronuclear Myopathy with Dilated Cardiomyopathy. The American Journal of Human Genetics. 95(2). 218–226. 115 indexed citations

Özcan, H. Nursun, Berna Oğuz, Beril Talim, Saniye Ekinci, & Mithat Haliloğlu. (2014). Unusual splenic hemangioma of a pediatric patient: hypointense on T2-weighted image. Clinical Imaging. 38(4). 553–555. 2 indexed citations

Merlini, Luciano, Monia Gennari, Elisabetta Malaspina, et al.. (2012). Early corticosteroid treatment in 4 duchenne muscular dystrophy patients: 14‐year follow‐up. Muscle & Nerve. 45(6). 796–802. 88 indexed citations

10.

Hara, Yuko, Burcu Balcı-Hayta, Takako Yoshida‐Moriguchi, et al.. (2011). BRIEF REPORT A Dystroglycan Mutation Associated with Limb-Girdle Muscular Dystrophy. UCL Discovery (University College London).

11.

Gündeşli, Hülya, Beril Talim, Petek Korkusuz, et al.. (2010). Mutation in Exon 1f of PLEC, Leading to Disruption of Plectin Isoform 1f, Causes Autosomal-Recessive Limb-Girdle Muscular Dystrophy. The American Journal of Human Genetics. 87(6). 834–841. 79 indexed citations

12.

Talim, Beril. (2009). Akut Respiratuvar Distres Sendromu. 5(2). 16–21. 1 indexed citations

13.

Talim, Beril, et al.. (2007). C.P.2.12 Congenital muscular dystrophy with mental retardation, dilated cardiomyopathy and abnormally located mitochondria. Neuromuscular Disorders. 17(9-10). 847–847. 1 indexed citations

14.

Merlini, Luciano, Christian Dohna‐Schwake, Maria Jędrzejowska, et al.. (2007). G.P.2.15 EUROSMART: European Spinal Muscular Atrophy Randomised Placebo-Controlled Trial of acetyl-L-carnitine in spinal muscular atrophy. Neuromuscular Disorders. 17(9-10). 780–781. 2 indexed citations

15.

Merlini, Luciano, et al.. (2007). G.P.1.02 10 years follow-up of early corticosteroid treatment of Duchenne muscular dystrophy. Neuromuscular Disorders. 17(9-10). 772–772.

16.

Gempel, Klaus, Haluk Topaloğlu, Beril Talim, et al.. (2007). The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene. Brain. 130(8). 2037–2044. 231 indexed citations

17.

Hoffmann, Katrin, Juliane Müller, Sigmar Stricker, et al.. (2006). Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit. The American Journal of Human Genetics. 79(2). 303–312. 100 indexed citations

18.

Kalaydjieva, Luba, Hanns Lochmüller, Ivailo Tournev, et al.. (2004). 125th ENMC International Workshop: Neuromuscular Disorders in the Roma (Gypsy) Population, 23–25 April 2004, Naarden, The Netherlands. Neuromuscular Disorders. 15(1). 65–71. 22 indexed citations

19.

Merlini, Luciano, Rebecca Gooding, Hanns Lochmüller, et al.. (2002). Genetic identity of Marinesco–Sjogren/myoglobinuria and CCFDN syndromes. Neurology. 58(2). 231–236. 25 indexed citations

20.

Çiftçi, Arbay Ö., et al.. (1999). Pulmonary lymphomatoid granulomatosis in a 4 year old. Journal of Pediatric Surgery. 34(6). 1033–1035. 10 indexed citations

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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