Haluk Topaloğlu

23.0k citations

266 papers · 9.0k · 4 hit papers · h-index 50

Impact in

Genetics top 0.5%
- Neurogenetic and Muscular Disorders Research
Cellular and Molecular Neuroscience top 1%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders

Papers in

Molecular Biology 167
- Muscle Physiology and Disorders 114
- Mitochondrial Function and Pathology 31
- RNA modifications and cancer 23
Genetics 56
- Neurogenetic and Muscular Disorders Research 54

Co-authors: Beril Talim (54 shared papers)Pascale Guicheney (21 shared papers)Göknur Haliloğlu (34 shared papers)Corinne Cruaud (4 shared papers)F.M.S. Tomé (6 shared papers)Michel Fardeau (6 shared papers)A. Leclerc (8 shared papers)Luciano Merlini (16 shared papers)
Journals: Neuromuscular Disorders (62 papers)Neuropediatrics (16 papers)European Journal of Paediatric Neurology (10 papers)Neurology (9 papers)Pediatric Neurology (8 papers)
Partner nations: Türkiye United States United Kingdom

In The Last Decade

Haluk Topaloğlu

254 papers receiving 8.6k citations

Haluk Topaloğlu's Hit Papers

align trajectories log scale

European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force—Second revision 2021 · 273 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2021 Journal of the Peripheral Nervous System
2021 European Journal of Neurology
2001 Developmental Cell
1995 Nature Genetics

Peers

Countries citing papers authored by Haluk Topaloğlu

Since Specialization

Citations

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

Fields of papers citing papers by Haluk Topaloğlu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Haluk Topaloğlu, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Haluk Topaloğlu Line = papers co-authored together Haluk Topaloğlu links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 266 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Muscular Dystrophy and Neuronal Migration Disorder Caused by Mutations in a Glycosyltransferase, POMGnT1 Developmental Cell ·Aruto Yoshida, Kazuhiro Kobayashi, Hiroshi Manya, Kiyomi Taniguchi, Hiroki Kano, Mamoru Mizuno, Toshiyuki Inazu, Hideyo Mitsuhashi, Seiichiro Takahashi, Makoto Takeuchi, Ralf Herrmann, Volker Straub, Beril Talim, Thomas Voit, Haluk Topaloğlu, Tatsushi Toda, Tamao Endo Hit paper breakdown →	2001	594
2	Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy Nature Genetics ·A. Leclerc, Xu Zhang, Haluk Topaloğlu, Corinne Cruaud, Frédérique Tesson, Jean Weissenbach, F.M.S. Tomé, Ketty Schwartz, Michel Fardeau, Karl Tryggvason, Pascale Guicheney Hit paper breakdown →	1995	532
3	The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy Nature Genetics ·Pascale Bomont, L Cavalier, F Blondeau, Christiane Ben Hamida, Samir Belal, Mériem Tazir, Ercan Demir, Haluk Topaloğlu, Rudolf Korinthenberg, Beyhan Tüysüz, P. Landrieu, Fayçal Hentati, (unknown)	2000	337
4	European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force—Second revision Journal of the Peripheral Nervous System ·Peter Van den Bergh, Pieter A. van Doorn, Robert D. M. Hadden, Bert Avau, Patrik Vankrunkelsven, Jeffrey A. Allen, Shahram Attarian, Patricia H. Blomkwist‐Markens, David R. Cornblath, Filip Eftimov, H. Stephan Goedee, Thomas Harbo, Satoshi Kuwabara, Richard A. Lewis, Michael P. Lunn, Eduardo Nobile‐Orazio, Luís Querol, Yusuf A. Rajabally, Claudia Sommer, Haluk Topaloğlu Hit paper breakdown →	2021	273
5	Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome Nature Genetics ·Behzad Moghadaszadeh, Nathalie Petit, Céline Jaillard, Martin Brockington, Susana Quijano Roy, Luciano Merlini, Norma B. Romero, B. Estournet, Isabelle Desguerre, Denys Chaigne, Francesco Muntoni, Haluk Topaloğlu, Pascale Guicheney	2001	271
6	The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene Brain ·Klaus Gempel, Haluk Topaloğlu, Beril Talim, Peter Schneiderat, Benedikt Schoser, Volkmar Hans, Beatrix Pálmafy, Gülsev Kale, Ayşegül Tokatlı, Catarina M. Quinzii, Michio Hirano, Ali Naini, Salvatore DiMauro, Holger Prokisch, Hanns Lochmüller, Rita Horváth	2007	259
7	European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force—Second revision European Journal of Neurology ·Peter Van den Bergh, Pieter A. van Doorn, Robert D. M. Hadden, Bert Avau, Patrik Vankrunkelsven, Jeffrey A. Allen, Shahram Attarian, Patricia H. Blomkwist‐Markens, David R. Cornblath, Filip Eftimov, H. Stephan Goedee, Thomas Harbo, Satoshi Kuwabara, Richard A. Lewis, Michael P. Lunn, Eduardo Nobile‐Orazio, Luís Querol, Yusuf A. Rajabally, Claudia Sommer, Haluk Topaloğlu Hit paper breakdown →	2021	257
8	Deciphering the Glycosylome of Dystroglycanopathies Using Haploid Screens for Lassa Virus Entry Science ·Lucas T. Jae, Matthijs Raaben, Moniek Riemersma, Ellen van Beusekom, Vincent A. Blomen, Arno Velds, Ron Kerkhoven, Jan E. Carette, Haluk Topaloğlu, Peter Meinecke, Marja W. Wessels, Dirk J. Lefeber, Sean P. J. Whelan, Hans van Bokhoven, Thijn R. Brummelkamp	2013	232
9	Mutations in the Gene Encoding Gap Junction Protein α12 (Connexin 46.6) Cause Pelizaeus-Merzbacher–Like Disease The American Journal of Human Genetics ·Birgit Uhlenberg, Markus Schuelke, Franz Rüschendorf, Nico Ruf, Angela M. Kaindl, Marco Henneke, Hölger Thiele, Gisela Stoltenburg‐Didinger, Fuat Aksu, Haluk Topaloğlu, Peter Nürnberg, Christoph Hübner, Bernhard Weschke, Jutta Gärtner	2004	232
10	Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia) Nature Genetics ·Sophie Nicole, Claire-Sophie Davoine, Haluk Topaloğlu, Laurence Cattolico, Duarte C. Barral, Peter Beighton, Christiane Ben Hamida, Hadi Hammouda, Corinne Cruaud, Peter S. White, Delphine Samson, J. Andoni Urtizberea, F. Lehmann‐Horn, Jean Weissenbach, Fayçal Hentati, Bertrand Fontaine	2000	228
11	A Dystroglycan Mutation Associated with Limb-Girdle Muscular Dystrophy 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	2011	204
12	Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy Nature Genetics ·Ingo Kurth, Torsten Pamminger, J. Christopher Hennings, Désirée Soehendra, Antje K. Huebner, Annelies Rotthier, Jonathan Baets, Jan Senderek, Haluk Topaloğlu, Sandra A. Farrell, Gudrun Nürnberg, Peter Nürnberg, Peter De Jonghe, Andreas Gal, Christoph Kaether, Vincent Timmerman, Christian A. Hübner	2009	195
13	An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker–Warburg syndrome (WWS) caused by a mutation in the POMT1 gene Neuromuscular Disorders ·Burcu Balcı, Gökhan Uyanık, Pervin Dinçer, Claudia Groß, Tobias Willer, Beril Talim, Göknur Haliloğlu, Gülsev Kale, Ute Hehr, Jürgen Winkler, Haluk Topaloğlu	2005	136
14	Clinical and genetic distinction between Walker–Warburg syndrome and muscle–eye–brain disease Neurology ·Bru Cormand, Helena Pihko, Mónica Bayés, Leena Valanne, Pirkko Santavuori, Beril Talim, Ruth Gershoni‐Baruch, Arsalan Ahmad, Hans van Bokhoven, Han G. Brunner, Thomas Voit, Haluk Topaloğlu, William B. Dobyns, Ana-Elina Lehesjoki	2001	133
15	Mutations in COL6A3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy The American Journal of Human Genetics ·Ercan Demir, Patrizia Sabatelli, Valérie Allamand, Ana Ferreiro, Behzad Moghadaszadeh, Mohamed Makrelouf, Haluk Topaloğlu, Bernard Échenne, Luciano Merlini, Pascale Guicheney	2002	131
16	A homozygous nonsense mutation in the Fukutin gene causes a Walker-Warburg syndrome phenotype Journal of Medical Genetics ·Daniel Beltrán Valero de Bernabé, Hans van Bokhoven, Ellen van Beusekom, Willem M.R. van den Akker, Sarina G. Kant, William B. Dobyns, Bru Cormand, Sophie Currier, Ben C.J. Hamel, Beril Talim, Haluk Topaloğlu, Han G. Brunner	2003	126
17	Mutations in GDAP1 Neurology ·Eva Nelis, Sevim Erdem‐Özdamar, Peter Van den Bergh, Marie‐Claude Belpaire‐Dethiou, C. Ceuterick, Veerle Van Gerwen, Ana Cuesta, Laia Pedrola, Francesc Palau, A.A.W.M. Gabreëls‐Festen, Christine Verellen, Ersin Tan, Mehmet Demirci, Christine Van Broeckhoven, Peter De Jonghe, Haluk Topaloğlu, Vincent Timmerman	2002	123
18	Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy Is Caused by Mutations in ASAH1 The American Journal of Human Genetics ·(unknown), Marcel Tawk, Francesco Danilo Tiziano, Julien Veillet, Mónica Bayés, Flora Nolent, Virginie Garcia, Serenella Servidei, Enrico Bertini, Francesc Castro-Giner, Yavuz Renda, Stéphane Carpentier, Nathalie Andrieu‐Abadie, Marta Gut, Thierry Levade, Haluk Topaloğlu, Judith Melki	2012	118
19	Assignment of the Muscle-Eye-Brain Disease Gene to 1p32-p34 by Linkage Analysis and Homozygosity Mapping The American Journal of Human Genetics ·Bru Cormand, Kristiina Avela, Helena Pihko, Pirkko Santavuori, Beril Talim, Haluk Topaloğlu, Albert de la Chapelle, Anna‐Elina Lehesjoki	1999	108
20	Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion European Journal of Human Genetics ·Onur Emre Onat, Süleyman Gülsüner, Kaya Bilgüvar, A. Nazlı Başak, Haluk Topaloğlu, Meli̇ha Tan, Üner Tan, Murat Günel, Tayfun Özçelık	2012	104

About Haluk Topaloğlu

Haluk Topaloğlu is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Neurology and Surgery, having authored 266 papers that have together received 9.0k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (114 papers), Neurogenetic and Muscular Disorders Research (54 papers), Mitochondrial Function and Pathology (31 papers), Genetic Neurodegenerative Diseases (28 papers), RNA modifications and cancer (23 papers), Cardiomyopathy and Myosin Studies (21 papers), Hereditary Neurological Disorders (19 papers) and Metabolism and Genetic Disorders (16 papers). The work is most often cited by research in Genetics (994 citations), Cellular and Molecular Neuroscience (1.8k citations), Cell Biology (1.4k citations), Immunology and Allergy (484 citations) and Neurology (1.2k citations). Haluk Topaloğlu has collaborated with scholars based in Türkiye, United States and United Kingdom. Frequent co-authors include Beril Talim, Pascale Guicheney, Göknur Haliloğlu, Corinne Cruaud, F.M.S. Tomé, Michel Fardeau, A. Leclerc, Luciano Merlini, Thomas Voit and Francesco Muntoni. Their work appears in journals such as Neuromuscular Disorders, Neuropediatrics, European Journal of Paediatric Neurology, Neurology and Pediatric Neurology.

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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Haluk Topaloğlu

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