A.L. Mosca

644 citations
12 papers · 529 · h-index 9

Impact in

  • Genetics top 10%
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases
    • Genetic Associations and Epidemiology
    • Autism Spectrum Disorder Research

Papers in

    • Genomic variations and chromosomal abnormalities 10
    • Congenital Ear and Nasal Anomalies 2
    • Genetic Syndromes and Imprinting 2
    • Genetics and Neurodevelopmental Disorders 2
    • Prenatal Screening and Diagnostics 3
    • Fetal and Pediatric Neurological Disorders 2

A.L. Mosca

12 papers receiving 484 citations

Peers

A.L. Mosca
Comparison fields: 5 of 57
  • Genetics 358
  • Cognitive Neuroscience 129
  • Molecular Biology 202
  • Pediatrics, Perinatology and Child Health 52
  • Psychiatry and Mental health 29
Replace Britt Marie Anderlid with:
Britt Marie Anderlid Sweden
Sui Yu Australia
Géraldine Joly‐Hélas France
Jessica R. Wolff United States
Jónas G. Halldórsson Iceland
Nora Urraca United States
Heather C. Mefford United States
Laura B. K. Herzing United States
Elyse B. Mitchell United States
Eric C. Crawford United States
A.L. Mosca relative to Britt Marie Anderlid Sweden Britt Marie Anderlid's profile →
Citations per field
00.5×1.7×
Britt Marie Anderlid · 1×
Citations per year

Countries citing papers authored by A.L. Mosca

Since Specialization
Citations

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

Fields of papers citing papers by A.L. Mosca

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside A.L. Mosca, 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 A.L. Mosca Line = papers co-authored together A.L. Mosca links everyone, so they are left out of the graph.

All Works

12 of 12 papers shown
#Work
1 2009362
2 200931
3 200826
4 201325
5 200922
6 200913
7 200912
8 201011
9 200710
10 20079
11 20064
12 20114

About A.L. Mosca

A.L. Mosca is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Genetics, Plant Science and Molecular Biology, having authored 12 papers that have together received 529 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (4 papers), Prenatal Screening and Diagnostics (3 papers), Congenital Ear and Nasal Anomalies (2 papers), Fetal and Pediatric Neurological Disorders (2 papers), Genetic Syndromes and Imprinting (2 papers), Congenital heart defects research (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Genetics (358 citations), Cognitive Neuroscience (129 citations), Molecular Biology (202 citations), Pediatrics, Perinatology and Child Health (52 citations) and Psychiatry and Mental health (29 citations). A.L. Mosca has collaborated with scholars based in France and Switzerland. Frequent co-authors include Francine Mugneret, Laurence Olivier Faivre, Patrick Callier, Nathalie Marle, Alice Masurel‐Paulet, Christel Thauvin‐Robinet, Frédéric Huet, J. Teyssier, Julien Guy and Paul Sagot. Their work appears in journals such as European Journal of Medical Genetics, Prenatal Diagnosis, Clinical Genetics, American Journal of Medical Genetics Part A and Archives of General Psychiatry.

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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