Miguel Mitne‐Neto

2.8k total citations · 1 hit paper
23 papers, 1.2k citations indexed

About

Miguel Mitne‐Neto is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Miguel Mitne‐Neto has authored 23 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Neurology. Recurrent topics in Miguel Mitne‐Neto's work include Amyotrophic Lateral Sclerosis Research (6 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Myeloproliferative Neoplasms: Diagnosis and Treatment (4 papers). Miguel Mitne‐Neto is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (6 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Myeloproliferative Neoplasms: Diagnosis and Treatment (4 papers). Miguel Mitne‐Neto collaborates with scholars based in Brazil, United States and United Kingdom. Miguel Mitne‐Neto's co-authors include Helga Cristina Almeida da Silva, Agnes L. Nishimura, João Ricardo Mendes de Oliveira, Fernando Kok, Paul Skehel, Susan Middleton, Thomas H. Gillingwater, Mayana Zatz, Jeanette Webb and Antônio Richieri‐Costa and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

In The Last Decade

Miguel Mitne‐Neto

22 papers receiving 1.2k 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.

A Mutation in the Vesicle-Trafficking Protein VAPB Causes Late-Onset Spinal Muscular Atrophy and Amyotrophic Lateral Sclerosis

2004 757 citations Agnes L. Nishimura, Miguel Mitne‐Neto et al. The American Journal of Human Genetics profile →

Peers

Countries citing papers authored by Miguel Mitne‐Neto

Since Specialization

Citations

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

Fields of papers citing papers by Miguel Mitne‐Neto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Miguel Mitne‐Neto. 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 Miguel Mitne‐Neto. The network helps show where Miguel Mitne‐Neto may publish in the future.

Co-authorship network of co-authors of Miguel Mitne‐Neto

This figure shows the co-authorship network connecting the top 25 collaborators of Miguel Mitne‐Neto. A scholar is included among the top collaborators of Miguel Mitne‐Neto 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 Miguel Mitne‐Neto. Miguel Mitne‐Neto 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:

20 of 20 papers shown

#	Work	Indexed citations
1	Evaluation of pathogenic variants detected in high homology regions of the PMS2 gene. How effective is long-range PCR? 2024 ·Frontiers in Oncology ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Paulo Goberlânio de Barros Silva, Miguel Mitne‐Neto, (unknown), (unknown)	0
2	P075: Evaluation of PMS2 gene variant c.2182_2184delinsG by NGS in a Brazilian sample: How long-range PCR can solve homology? 2023 ·SHILAP Revista de lepidopterología ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Paulo Goberlânio de Barros Silva, Miguel Mitne‐Neto, (unknown), (unknown)	1
3	Genetic risk factors and COVID-19 severity in Brazil: results from BRACOVID study 2022 ·Human Molecular Genetics ·Alexandre C. Pereira, (unknown), (unknown), Emanuelle Marques, (unknown), (unknown), Carla Luana Dinardo, Sílvia Figueiredo Costa, Alberto J. S. Duarte, Alexandre Rosa dos Santos, Miguel Mitne‐Neto, José Medina‐Pestana, José Eduardo Krieger	12
4	Small-fibre Neuropathy in Patients with Familial Amyotrophic Lateral Sclerosis Type 8 2022 ·Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·Marcela Câmara Machado‐Costa, Miguel Mitne‐Neto, (unknown), (unknown), Acary Souza Bullé Oliveira, Mayana Zatz, Helga Cristina Almeida da Silva	2
5	JAK2-mutated acute myeloid leukemia: comparison of next-generation sequencing (NGS) and single nucleotide polymorphism array (SNPa) findings between two cases 2019 ·SHILAP Revista de lepidopterología ·(unknown), Miguel Mitne‐Neto, Maria de Lourdes Chauffaille	6
6	A novel GNRHR gene mutation causing congenital hypogonadotrophic hypogonadism in a Brazilian kindred 2018 ·Journal of Neuroendocrinology ·(unknown), (unknown), Marina M. L. Kizys, (unknown), David Santos Marco Antônio, (unknown), Gilberto K. Furuzawa, (unknown), Flavia Amanda Costa‐Barbosa, Miguel Mitne‐Neto, Magnus R. Dias‐da‐Silva	7
7	DUOX2 Mutations Are Associated With Congenital Hypothyroidism With Ectopic Thyroid Gland 2017 ·The Journal of Clinical Endocrinology & Metabolism ·Marina M. L. Kizys, Ruy A. Louzada, Miguel Mitne‐Neto, (unknown), Gilberto K. Furuzawa, Denise Pires de Carvalho, Magnus R. Dias‐da‐Silva, Suzana Nesi-França, Corinne Dupuy, Rui M. B. Maciel	43
8	Development and validation of a variant detection workflow for BRCA1 and BRCA2 genes and its clinical application based on the Ion Torrent technology 2017 ·Human Genomics ·(unknown), (unknown), (unknown), (unknown), (unknown), David Santos Marco Antônio, Caio Robledo D’Angioli Costa Quaio, Wagner Antonio da Rosa Baratela, Miguel Mitne‐Neto	8
9	Mutational Profiling of Acute Myeloid Leukemia with Normal Cytogenetics in Brazilian Patients: The Value of Next-Generation Sequencing for Genomic Classification 2017 ·Journal of Investigative Medicine ·(unknown), Miguel Mitne‐Neto, Maria de Lourdes Chauffaille	9
10	Different Donors Mesenchymal Stromal Cells Secretomes Reveal Heterogeneous Profile of Relevance for Therapeutic Use 2016 ·Stem Cells and Development ·Amanda F. Assoni, (unknown), Marcos Valadares, Melinda S. Beccari, Juliana Gomes, (unknown), Miguel Mitne‐Neto, Valdemir Melechco Carvalho, Mayana Zatz	52
11	CALR mutations screening in wild type JAK2V617F and MPLW515K/L Brazilian myeloproliferative neoplasm patients 2015 ·Blood Cells Molecules and Diseases ·(unknown), (unknown), Maria de Lourdes Chauffaille, Miguel Mitne‐Neto, (unknown), (unknown), Elvira Maria Guerra‐Shinohara	15
12	A Variant Detection Pipeline for Inherited Cardiomyopathy–Associated Genes Using Next-Generation Sequencing 2015 ·Journal of Molecular Diagnostics ·Théo Gremen Mimary de Oliveira, Miguel Mitne‐Neto, Louise Cerdeira, Júlia Daher Carneiro Marsiglia, Edmundo Arteaga-Fernández, José Eduardo Krieger, Alexandre C. Pereira	5
13	Stem cells for amyotrophic lateral sclerosis modeling and therapy: Myth or fact? 2015 ·Cytometry Part A ·(unknown), Melinda S. Beccari, (unknown), Miguel Mitne‐Neto, Oswaldo Keith Okamoto, Mayana Zatz	19
14	Complete Genome Sequence of an F8-Like Lytic Myovirus (φSPM-1) That Infects Metallo-β-Lactamase-Producing Pseudomonas aeruginosa 2014 ·Genome Announcements ·Patrícia Neves, Louise Cerdeira, Miguel Mitne‐Neto, Théo Gremen Mimary de Oliveira, John Anthony McCulloch, Jorge Luiz Mello Sampaio, Elsa M. Mamizuka, Carlos Emílio Levy, Maria Inês Zanoli Sato, Nilton Lincopán	4
15	Molecular genetic tests for JAK2 V617F, Exon12_ JAK2 and MPL W515K/L are highly informative in the evaluation of patients suspected to have BCR-ABL1-negative myeloproliferative neoplasms 2013 ·Journal of Clinical Pathology ·(unknown), Miguel Mitne‐Neto, (unknown), Maria de Lourdes Chauffaille, Edgar Gil Rizzatti	6
16	Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients 2011 ·Human Molecular Genetics ·Miguel Mitne‐Neto, Marcela Câmara Machado‐Costa, Maria C. Marchetto, Mário Henrique Bengtson, Claudio A.P. Joazeiro, Hiroshi Tsuda, Hugo J. Bellen, Helga Cristina Almeida da Silva, Acary Souza Bullé Oliveira, Monize Lazar, Alysson R. Muotri, Mayana Zatz	173
17	A mutation in human VAP-B–MSP domain, present in ALS patients, affects the interaction with other cellular proteins 2007 ·Protein Expression and Purification ·Miguel Mitne‐Neto, Celso R. Ramos, Daniel C. Pimenta, Juliana Silva da Luz, Agnes L. Nishimura, Fernando A. Gonzales-Zubiate, Carla C. Oliveira, Mayana Zatz	24
18	A multi-exonic SPG4 duplication underlies sex-dependent penetrance of hereditary spastic paraplegia in a large Brazilian pedigree 2007 ·European Journal of Human Genetics ·Miguel Mitne‐Neto, Fernando Kok, Christian Beetz, André Luiz Santos Pessoa, Clarissa Bueno, (unknown), (unknown), Carlos Bandeira de Mello Monteiro, (unknown), (unknown), Anders O.H. Nygren, Marcos Valadares, Antonia Cerqueira, Alessandra Starling, Thomas Deufel, Mayana Zatz	24
19	Lack of Association Between the Brain-Derived Neurotrophin Factor (C-270T) Polymorphism and Late-Onset Alzheimer's Disease (LOAD) in Brazilian Patients 2004 ·Journal of Molecular Neuroscience ·Agnes L. Nishimura, João Ricardo Mendes de Oliveira, Miguel Mitne‐Neto, Camila Guindalini, (unknown), Valéria Santoro Bahia, Paulo Roberto de Brito-Marques, Paulo Alberto Otto, Mayana Zatz	24
20	A Mutation in the Vesicle-Trafficking Protein VAPB Causes Late-Onset Spinal Muscular Atrophy and Amyotrophic Lateral Sclerosis breakdown → 2004 ·The American Journal of Human Genetics ·Agnes L. Nishimura, Miguel Mitne‐Neto, Helga Cristina Almeida da Silva, Antônio Richieri‐Costa, Susan Middleton, Duilio Cascio, Fernando Kok, João Ricardo Mendes de Oliveira, Thomas H. Gillingwater, Jeanette Webb, Paul Skehel, Mayana Zatz	757

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