Daniel Moreno‐De‐Luca

1.6k citations
16 papers · 690 · 1 hit paper · h-index 9

Impact in

    • Autism Spectrum Disorder Research
  • Genetics top 5%
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases

Papers in

    • Genomic variations and chromosomal abnormalities 9
    • Genetics and Neurodevelopmental Disorders 5
    • Genomics and Rare Diseases 4
    • BRCA gene mutations in cancer 2
    • Autism Spectrum Disorder Research 7

Daniel Moreno‐De‐Luca

14 papers receiving 679 citations

Daniel Moreno‐De‐Luca's Hit Papers

Autism genetics: opportunities and challenges for clinical translation 2017 · 310 citations
3100+3+6Years since publication100200300

Peers

Daniel Moreno‐De‐Luca
Comparison fields: 5 of 73
  • Cognitive Neuroscience 342
  • Genetics 338
  • Psychiatry and Mental health 84
  • Biological Psychiatry 11
  • Developmental Neuroscience 16
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Citations per year

Countries citing papers authored by Daniel Moreno‐De‐Luca

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Moreno‐De‐Luca

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel Moreno‐De‐Luca. 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 Daniel Moreno‐De‐Luca. The network helps show where Daniel Moreno‐De‐Luca may publish in the future.

Co-authors

The 25 scholars most cited alongside Daniel Moreno‐De‐Luca, 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 Daniel Moreno‐De‐Luca Line = papers co-authored together Daniel Moreno‐De‐Luca links everyone, so they are left out of the graph.

All Works

16 of 16 papers shown
#Work
1
Autism genetics: opportunities and challenges for clinical translation
Hit paper breakdown →
2017310
2 2013219
3 202037
4 201829
5 201021
6 202116
7
17q12 Recurrent Deletion Syndrome
202015
8 201914
9 202212
10 20178
11
What Should a Psychiatrist Know About Genetics? Review and Recommendations From the Residency Education Committee of the International Society of Psychiatric Genetics.
20185
12 20192
13 20191
14 20221
15 20250
16 20200

About Daniel Moreno‐De‐Luca

Daniel Moreno‐De‐Luca is a scholar working on Genetics, Cognitive Neuroscience, Molecular Biology, Organic Chemistry and Pediatrics, Perinatology and Child Health, having authored 16 papers that have together received 690 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Autism Spectrum Disorder Research (7 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers), Congenital heart defects research (3 papers), BRCA gene mutations in cancer (2 papers), Epigenetics and DNA Methylation (1 paper) and Nitric Oxide and Endothelin Effects (1 paper). The work is most often cited by research in Cognitive Neuroscience (342 citations), Genetics (338 citations), Psychiatry and Mental health (84 citations), Biological Psychiatry (11 citations) and Developmental Neuroscience (16 citations). Daniel Moreno‐De‐Luca has collaborated with scholars based in United States, Canada and Germany. Frequent co-authors include John I. Nürnberger, Joachim Hallmayer, Jacob Vorstman, Jeremy Parr, Richard Anney, Scott M. Myers, David H. Ledbetter, Thomas D. Challman, David W. Evans and Andrés Moreno-De-Luca. Their work appears in journals such as JAMA Psychiatry, BMC Genetics, Current Opinion in Genetics & Development, European Neuropsychopharmacology and The Lancet 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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