A Alberti

3k citations
38 papers · 2.3k · 3 hit papers · h-index 14

Impact in

  • Genetics top 2%
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Autism Spectrum Disorder Research

Papers in

    • Genomic variations and chromosomal abnormalities 5
    • Genetics and Neurodevelopmental Disorders 5
    • Dermatological and Skeletal Disorders 2
    • Genetic and rare skin diseases. 2
    • Growth Hormone and Insulin-like Growth Factors 6

A Alberti

38 papers receiving 2.2k citations

A Alberti's Hit Papers

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases 2017 · 424 citations
4240+4+8Years since publication200400600

Peers

A Alberti
Comparison fields: 5 of 91
  • Genetics 1.2k
  • Cognitive Neuroscience 663
  • Developmental Neuroscience 64
  • Psychiatry and Mental health 124
  • Pediatrics, Perinatology and Child Health 73
Replace Roberto Militerni with:
Roberto Militerni Italy
Alicia Guemez‐Gamboa United States
Vera Stoppioni Italy
Noriyoshi Usui Japan
Matthew J. Gazzellone Canada
Thomas D. Challman United States
Jessica A. Burket United States
Susanne M. Cabrera United States
Rebecca L. Walker United States
Masaaki Narita Japan
A Alberti relative to Roberto Militerni Italy Roberto Militerni's profile →
Citations per field
00.5×2×3×3.6×
Roberto Militerni · 1×
Citations per year

Countries citing papers authored by A Alberti

Since Specialization
Citations

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

Fields of papers citing papers by A Alberti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 38 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development
Hit paper breakdown →
2014602
2
Refining analyses of copy number variation identifies specific genes associated with developmental delay
Hit paper breakdown →
2014541
3
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
Hit paper breakdown →
2017424
4 2017148
5 2016127
6 1999120
7 200749
8 201536
9 200733
10 201822
11
Comparison of three probiotics in the treatment of acute diarrhea in mentally retarded children.
200016
12 199415
13 199615
14 201414
15 199912
16 199611
17
IGF-I levels in prepubertal and pubertal children with Down syndrome.
199810
18 200210
19 19979
20
Mees' lines due to cyclosporin.
19999

About A Alberti

A Alberti is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism, Public Health, Environmental and Occupational Health, Anesthesiology and Pain Medicine and Reproductive Medicine, having authored 38 papers that have together received 2.3k indexed citations. Recurring topics across this work include Down syndrome and intellectual disability research (7 papers), Growth Hormone and Insulin-like Growth Factors (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Anesthesia and Sedative Agents (3 papers), Dermatological and Skeletal Disorders (2 papers), Genetic and rare skin diseases. (2 papers) and Reproductive Biology and Fertility (2 papers). The work is most often cited by research in Genetics (1.2k citations), Cognitive Neuroscience (663 citations), Developmental Neuroscience (64 citations), Psychiatry and Mental health (124 citations) and Pediatrics, Perinatology and Child Health (73 citations). A Alberti has collaborated with scholars based in Italy, United States and Netherlands. Frequent co-authors include Corrado Romano, Maurizio Elia, Rosemary H. Waring, Carmelo Schepis, Maddalena Siragusa, Ornella Galesi, Marco Fichera, Letizia Ragusa, Pinella Failla and Caterina Proto. Their work appears in journals such as Clinical Genetics, Nature Genetics, Dermatology, Biological Psychiatry and Acta Dermato Venereologica.

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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