Montserrat Milà

6.1k citations
140 papers · 4.0k indexed · 1 hit paper · h-index 34
Topics
Genetics and Neurodevelopmental Disorders (60 papers)Genomic variations and chromosomal abnormalities (38 papers)Autism Spectrum Disorder Research (32 papers)

In The Last Decade

Montserrat Milà

139 papers receiving 3.9k citations

Hit Papers

Connexin-26 mutations in sporadic and inherited sensorine...19982026200720161998100200300400500

Peers

Montserrat Milà
Comparison fields: 5 of 105
  • Molecular Biology 2.2k
  • Genetics 1.8k
  • Cognitive Neuroscience 934
  • Sensory Systems 690
  • Cellular and Molecular Neuroscience 511
Replace Daryl A. Scott with:
Daryl A. Scott United States
Kimia Kahrizi Iran
Raquel Rabionet Spain
Helger G. Yntema Netherlands
Donna M. Martin United States
Carlos A. Bacino United States
Kerstin Kutsche Germany
Lorraine Potocki United States
Yvan Arsenijévic Switzerland
Bai-Lin Wu United States
Montserrat Milà relative to Daryl A. Scott United States Daryl A. Scott's profile →
Citations per field
00.5×
Daryl A. Scott · 1×
Citations per year

Countries citing papers authored by Montserrat Milà

Since Specialization
Citations

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

Fields of papers citing papers by Montserrat Milà

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Montserrat Milà

This figure shows the co-authorship network connecting the top 25 collaborators of Montserrat Milà. A scholar is included among the top collaborators of Montserrat Milà 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 Montserrat Milà. Montserrat Milà 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
#WorkIndexed citations
1 8
2 3
3 13
4 8
5 11
6 47
7 74
8 10
9 7
10 23
11 31
12 14
13 1
14 3
15 12
16 44
17 72
18
[Molecular analysis of the IT15 gene in 79 Spanish families with Huntington's disease: diagnostic confirmation and presymptomatic diagnosis].
3
19 10
20
Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins.
79

About Montserrat Milà

Montserrat Milà is a scholar working on Genetics, Cognitive Neuroscience and Cellular and Molecular Neuroscience, having authored 140 papers that have together received 4.0k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (60 papers), Genomic variations and chromosomal abnormalities (38 papers) and Autism Spectrum Disorder Research (32 papers). The work is most often cited by research in Sensory Systems (690 citations), Genetics (1.8k citations) and Cognitive Neuroscience (934 citations). Montserrat Milà has collaborated with scholars based in Spain, United States and Netherlands. Frequent co-authors include Célia Bádenas, Laia Rodríguez‐Revenga, Irene Madrigal, Xavier Estivill, Aurora Sánchez, Nancy Govea, Paolo Gasparini, Paolo Fortina, Leopoldo Zelante and Saul Surrey. Their work appears in journals such as The Lancet, Journal of Clinical Oncology and 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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