Berge A. Minassian

646 total citations
16 papers, 265 citations indexed

About

Berge A. Minassian is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Berge A. Minassian has authored 16 papers receiving a total of 265 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Rheumatology. Recurrent topics in Berge A. Minassian's work include Glycogen Storage Diseases and Myoclonus (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomics and Rare Diseases (3 papers). Berge A. Minassian is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomics and Rare Diseases (3 papers). Berge A. Minassian collaborates with scholars based in Canada, United States and Italy. Berge A. Minassian's co-authors include Patrick Cossette, Felippe Borlot, Danielle M. Andrade, Fábio A. Nascimento, Alessandra Ruggieri, Susan Arnold, Brandy Verhalen, N. Ramachandran, Peixiang Wang and Charles A. Steward and has published in prestigious journals such as PLoS ONE, Neurology and Annals of Neurology.

In The Last Decade

Berge A. Minassian

15 papers receiving 262 citations

Peers

Countries citing papers authored by Berge A. Minassian

Since Specialization

Citations

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

Fields of papers citing papers by Berge A. Minassian

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Berge A. Minassian. 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 Berge A. Minassian. The network helps show where Berge A. Minassian may publish in the future.

Co-authorship network of co-authors of Berge A. Minassian

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Myofiber-type-dependent ‘boulder’ or ‘multitudinous pebble’ formations across distinct amylopectinoses 2024 ·Acta Neuropathologica ·Sharmistha Mitra, Baozhi Chen, John M. Shelton, Silvia Nitschke, Jun Wu, (unknown), (unknown), (unknown), Mayank Verma, Felix Nitschké, (unknown), Kazuhiro Iwaï, Bret M. Evers, Berge A. Minassian	3
2	Unraveling the role of non-coding rare variants in epilepsy 2023 ·PLoS ONE ·(unknown), Claudia Moreau, Jacques L. Michaud, Berge A. Minassian, Patrick Cossette, Simon Girard	0
3	Polygenic risk scores of several subtypes of epilepsies in a founder population 2020 ·Neurology Genetics ·Claudia Moreau, Rose‐Marie Rébillard, Stefan Wolking, Jacques L. Michaud, (unknown), (unknown), (unknown), Berge A. Minassian, Catherine Laprise, Patrick Cossette, Simon Girard	14
4	Multiomic elucidation of a coding 99-mer repeat-expansion skeletal muscle disease 2020 ·Acta Neuropathologica ·Alessandra Ruggieri, Sergey Naumenko, Martin A. Smith, (unknown), Flavia Blàsevich, Cinzia Bragato, Sara Gibertini, Kirston Barton, Matthias Vorgerd, Katrin Marcus, Peixiang Wang, Lorenzo Maggi, Renato Mantegazza, James J. Dowling, Rudolf A. Kley, Marina Mora, Berge A. Minassian	22
5	Dominant LMAN2L mutation causes intellectual disability with remitting epilepsy 2019 ·Annals of Clinical and Translational Neurology ·Reem A. Alkhater, Peixiang Wang, Alessandra Ruggieri, (unknown), Susan Walker, Stephen W. Scherer, Mary Lou Smith, Berge A. Minassian	7
6	Lafora Disease: A Review of Molecular Mechanisms and Pathology 2018 ·Neuropediatrics ·Brandy Verhalen, Susan Arnold, Berge A. Minassian	18
7	Lafora disease in miniature Wirehaired Dachshunds 2017 ·PLoS ONE ·(unknown), (unknown), (unknown), Saija Ahonen, Peixiang Wang, Cameron Ackerley, Berge A. Minassian, Clare Rusbridge	21
8	Genome annotation for clinical genomic diagnostics: strengths and weaknesses 2017 ·Genome Medicine ·Charles A. Steward, Alasdair Parker, Berge A. Minassian, Sanjay M. Sisodiya, Adam Frankish, Jennifer Harrow	30
9	Epileptic Encephalopathy Caused by Mutations in the Guanine Nucleotide Exchange Factor DENND5A 2016 ·The American Journal of Human Genetics ·Chanshuai Han, Reem A. Alkhater, Tawfiq Froukh, (unknown), Melissa A. Galati, (unknown), Maryam Fotouhi, (unknown), (unknown), Christian R. Marshall, Susan Walker, Peter Bauer, Stephen W. Scherer, Olaf Rieß, Rebecca Buchert, Berge A. Minassian, Peter S. McPherson	27
10	An exon trap with proper poly-A site in the GBE1 is the common missing cause in Adult Polyglucosan Body Disease (S42.006) 2015 ·Neurology ·(unknown), Or Kakhlon, Jorida Çoku, Lorenzo Peverelli, Hanna Rosenmann, (unknown), Julie Turnbull, Vardiella Meiner, (unknown), Israela Lerer, Shoshi Shpitzen, Eran Leitersdorf, (unknown), Mary Wallace, Raphael Schiffmann, Salvatore DiMauro, Alexander Lossos, Berge A. Minassian	1
11	Two definite cases of sudden unexpected death in epilepsy in a family with a DEPDC5 mutation 2015 ·Neurology Genetics ·Fábio A. Nascimento, Felippe Borlot, Patrick Cossette, Berge A. Minassian, Danielle M. Andrade	43
12	Congenital autophagic vacuolar myopathy is allelic to X-linked myopathy with excessive autophagy 2015 ·Neurology ·Iulia Munteanu, N. Ramachandran, Alessandra Ruggieri, Tomonari Awaya, Ichizo Nishino, Berge A. Minassian	16
13	Deep IntronicGBE1Mutation in Manifesting Heterozygous Patients With Adult Polyglucosan Body Disease 2015 ·JAMA Neurology ·Hasan O. Akman, Or Kakhlon, Jorida Çoku, Lorenzo Peverelli, Hanna Rosenmann, (unknown), Julie Turnbull, Vardiella Meiner, (unknown), Israela Lerer, Shoshi Shpitzen, Eran Leitersdorf, Carmen Paradas, Mary Wallace, Raphael Schiffmann, Salvatore DiMauro, Alexander Lossos, Berge A. Minassian	30
14	Late adult‐onset of X‐linked myopathy with excessive autophagy 2014 ·Muscle & Nerve ·(unknown), Alessandra Ruggieri, Meena Gujrati, (unknown), N. Ramachandran, Berge A. Minassian, Steven A. Moore	20
15	The Genetics of a Novel Form of Lafora Disease 2010 ·Julie Turnbull, Jean‐Marie Girard, Hannes Lohi, Elayne M. Chan, (unknown), (unknown), Salah Omer, Mushtaq Ahmed, Chris Bennett, Aruna Chakrabarty, Nela Pencea, Xiaochu Zhao, Stephen W. Scherer, Cameron Ackerley, Berge A. Minassian	5
16	Electrophysiological findings in X‐linked myopathy with excessive autophagy 2002 ·Annals of Neurology ·Satu K. Jääskeläinen, Vern C. Juel, Bjarne Udd, Marcello Villanova, Rocco Liguori, Berge A. Minassian, Björn Falck, Pekka Niemi, Hannu Kalimo	8

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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