John Anthony Crolla

11.9k citations
139 papers · 9.0k · 2 hit papers · h-index 44

Impact in

  • Genetics top 0.2%
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Prenatal Screening and Diagnostics

Papers in

    • Genomic variations and chromosomal abnormalities 69
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 14
    • Genetic Syndromes and Imprinting 14
    • Genetics and Neurodevelopmental Disorders 12
    • Prenatal Screening and Diagnostics 36

John Anthony Crolla

136 papers receiving 8.2k citations

John Anthony Crolla's Hit Papers

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies 2010 · 2.2k citations
2.2k0+6+12Years since publication50010001.5k2.0k

Peers

John Anthony Crolla
Comparison fields: 5 of 119
  • Genetics 6.0k
  • Pediatrics, Perinatology and Child Health 2.1k
  • Molecular Biology 3.4k
  • Genetics 504
  • Plant Science 1.3k
Replace Blake C. Ballif with:
Blake C. Ballif United States
Samantha J.L. Knight United Kingdom
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Citations per field
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Citations per year

Countries citing papers authored by John Anthony Crolla

Since Specialization
Citations

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

Fields of papers citing papers by John Anthony Crolla

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John Anthony Crolla. 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 John Anthony Crolla. The network helps show where John Anthony Crolla may publish in the future.

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 139 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
Hit paper breakdown →
20102162
2
Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
Hit paper breakdown →
2008629
3 2011352
4 2010266
5 2009260
6 1976229
7 2008155
8 2002148
9 1995146
10 2001142
11 1998141
12 2013141
13 2008137
14 2002136
15 2005112
16 2005104
17 2008102
18 1996100
19 200099
20 199097

About John Anthony Crolla

John Anthony Crolla is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Plant Science and Genetics, having authored 139 papers that have together received 9.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (69 papers), Prenatal Screening and Diagnostics (36 papers), Chromosomal and Genetic Variations (34 papers), Genomics and Chromatin Dynamics (17 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers), Genetic Syndromes and Imprinting (14 papers), Congenital heart defects research (13 papers) and Genetics and Neurodevelopmental Disorders (12 papers). The work is most often cited by research in Genetics (6.0k citations), Pediatrics, Perinatology and Child Health (2.1k citations), Molecular Biology (3.4k citations), Genetics (504 citations) and Plant Science (1.3k citations). John Anthony Crolla has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Veronica van Heyningen, Michael R. Creasy, Patricia A. Jacobs, P. A. Jacobs, Annette E. Cockwell, Eva D. Alberman, I. Karen Temple, David Owen Robinson, Nicholas Simon Thomas and Nick R Dennis. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, European Journal of Human Genetics, The American Journal of Human Genetics and Prenatal Diagnosis.

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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