Pedro Mancías

3.1k total citations
37 papers, 1.7k citations indexed

About

Pedro Mancías is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Pedro Mancías has authored 37 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 7 papers in Neurology. Recurrent topics in Pedro Mancías's work include Hereditary Neurological Disorders (7 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Neurological diseases and metabolism (3 papers). Pedro Mancías is often cited by papers focused on Hereditary Neurological Disorders (7 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Neurological diseases and metabolism (3 papers). Pedro Mancías collaborates with scholars based in United States, Japan and United Kingdom. Pedro Mancías's co-authors include Ian J. Butler, James R. Lupski, Laura Davis Keppen, Laura E. Warner, Craig M. McDonald, Mehrdad Khajavi, Ken Inoue, James D. Reggin, Miles Wilkinson and Michael Wegner and has published in prestigious journals such as Nature Genetics, Neurology and Annals of Neurology.

In The Last Decade

Pedro Mancías

34 papers receiving 1.7k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Pedro Mancías United States 15 809 750 380 280 228 37 1.7k
Velina Guergueltcheva Bulgaria 23 561 0.7× 899 1.2× 408 1.1× 213 0.8× 308 1.4× 52 1.6k
Theodoros Kyriakides Cyprus 17 509 0.6× 938 1.3× 221 0.6× 170 0.6× 231 1.0× 47 1.5k
Peter H. Larsen Canada 19 433 0.5× 762 1.0× 320 0.8× 360 1.3× 101 0.4× 28 2.1k
Alessandro Filla Italy 24 1.0k 1.2× 949 1.3× 498 1.3× 191 0.7× 145 0.6× 45 1.6k
Alessandro Malandrini Italy 26 591 0.7× 973 1.3× 577 1.5× 546 1.9× 210 0.9× 95 2.2k
Teresa Sevilla Spain 27 1.2k 1.5× 759 1.0× 846 2.2× 526 1.9× 245 1.1× 102 2.3k
Hillary Lipe United States 24 945 1.2× 593 0.8× 600 1.6× 210 0.8× 123 0.5× 40 1.5k
Emilia Bellone Italy 24 1.0k 1.3× 681 0.9× 787 2.1× 405 1.4× 195 0.9× 100 1.8k
Gian Maria Fabrizi Italy 22 891 1.1× 686 0.9× 540 1.4× 313 1.1× 310 1.4× 88 1.6k
A. Löfgren Belgium 18 878 1.1× 1.1k 1.5× 304 0.8× 308 1.1× 164 0.7× 37 1.8k

Countries citing papers authored by Pedro Mancías

Since Specialization
Citations

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

Fields of papers citing papers by Pedro Mancías

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pedro Mancías

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

All Works

20 of 20 papers shown
1.
Northrup, Hope, et al.. (2022). Identification of a novel microdeletion causative of Nance‐Horan syndrome. Molecular Genetics & Genomic Medicine. 10(3). e1879–e1879. 4 indexed citations
2.
Koenig, Mary Kay, et al.. (2021). A De Novo case of autosomal dominant mitochondrial membrane protein‐associated neurodegeneration. Molecular Genetics & Genomic Medicine. 9(7). e1706–e1706. 3 indexed citations
3.
Calame, Daniel G., Jawid M. Fatih, Isabella Herman, et al.. (2021). Biallelic Pathogenic Variants in TNNT3 Associated With Congenital Myopathy. Neurology Genetics. 7(3). e589–e589. 9 indexed citations
4.
5.
Sheikh, Kazim A., et al.. (2020). Uniparental Disomy Leading to a Rare Juvenile Form of ALS. PubMed. 4(4). 107–110. 1 indexed citations
6.
Watanabe, Seiji, Hristelina Ilieva, Hiromi Tamada, et al.. (2016). Mitochondria‐associated membrane collapse is a common pathomechanism in SIGMAR 1 ‐ and SOD 1 ‐linked ALS. EMBO Molecular Medicine. 8(12). 1421–1437. 201 indexed citations
7.
8.
Szigeti, Kinga, Wojciech Wiszniewski, Gulam Mustafa Saifi, et al.. (2007). Functional, histopathologic and natural history study of neuropathy associated with EGR2 mutations. Neurogenetics. 8(4). 257–262. 32 indexed citations
9.
Gruber, Scott A., et al.. (2006). Living-Donor Nerve Transplantation for Global Obstetric Brachial Plexus Palsy. Journal of Reconstructive Microsurgery. 22(4). 245–254. 7 indexed citations
10.
Saifi, Gulam Mustafa, Kinga Szigeti, Wojciech Wiszniewski, et al.. (2005). SIMPLEmutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation. Human Mutation. 25(4). 372–383. 73 indexed citations
11.
Heresi, Gloria P., et al.. (2004). POLIOMYELITIS-LIKE SYNDROME IN A CHILD WITH WEST NILE VIRUS INFECTION. The Pediatric Infectious Disease Journal. 23(8). 788–789. 23 indexed citations
12.
Shy, Michael E., Grace M. Hobson, Odile Boespflug‐Tanguy, et al.. (2003). Schwann cell expression of PLP1 but not DM20 is necessary to prevent neuropathy. Annals of Neurology. 53(3). 354–365. 50 indexed citations
13.
Ng, Yu-tze, Pedro Mancías, & Ian J. Butler. (2002). Lumbar Spinal Stenosis Causing Congenital Clubfoot. Journal of Child Neurology. 17(1). 72–74. 1 indexed citations
14.
Boerkoel, Cornelius F., Hiroshi Takashima, Carlos García, et al.. (2001). Charcot‐Marie‐Tooth disease and related neuropathies: Mutation distribution and genotype‐phenotype correlation. Annals of Neurology. 51(2). 190–201. 198 indexed citations
15.
Papanicolaou, Andrew C., Panagiotis G. Simos, Joshua I. Breier, et al.. (2001). Brain Plasticity for Sensory and Linguistic Functions: A Functional Imaging Study Using Magnetoencephalography With Children and Young Adults. Journal of Child Neurology. 16(4). 241–241. 3 indexed citations
16.
Tseng, Brian S., Eric P. Hoffman, Susan T. Iannaccone, et al.. (1999). Human bHLH Transcription Factor GeneMyogenin(MYOG): Genomic Sequence and Negative Mutation Analysis in Patients with Severe Congenital Myopathies. Genomics. 57(3). 419–423. 8 indexed citations
17.
Warner, Laura E., Pedro Mancías, Ian J. Butler, et al.. (1998). Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies. Nature Genetics. 18(4). 382–384. 373 indexed citations
18.
Pegoraro, Elena, Eric P. Hoffman, Pedro Mancías, et al.. (1996). Congenital muscular dystrophy with primary laminin α2 (merosin) deficiency presenting as inflammatory myopathy. Annals of Neurology. 40(5). 782–791. 82 indexed citations
19.
Williams, Jane, Mitzie Grant, Sarah J. Shema, et al.. (1996). Behavioral Descriptors that Differentiate Between Seizure and Nonseizure Events in a Pediatric Population. Clinical Pediatrics. 35(5). 243–249. 5 indexed citations
20.
Pagliaro, Lance C. & Pedro Mancías. (1994). Polymyositis associated with chronic myelogenous leukemia. Annals of Hematology. 68(4). 213–214. 3 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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