John A. Crolla

11.8k total citations
124 papers, 4.2k citations indexed

About

John A. Crolla is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, John A. Crolla has authored 124 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 92 papers in Genetics, 62 papers in Molecular Biology and 37 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in John A. Crolla's work include Genomic variations and chromosomal abnormalities (61 papers), Prenatal Screening and Diagnostics (36 papers) and Chromosomal and Genetic Variations (33 papers). John A. Crolla is often cited by papers focused on Genomic variations and chromosomal abnormalities (61 papers), Prenatal Screening and Diagnostics (36 papers) and Chromosomal and Genetic Variations (33 papers). John A. Crolla collaborates with scholars based in United Kingdom, United States and France. John A. Crolla's co-authors include M. R. Creasy, Veronica van Heyningen, P. A. Jacobs, Eva Alberman, Patricia A. Jacobs, David Robinson, Annette E. Cockwell, N R Dennis, N. Simon Thomas and Nicholas R. Dennis and has published in prestigious journals such as Nature, The Lancet and SHILAP Revista de lepidopterología.

In The Last Decade

John A. Crolla

123 papers receiving 3.9k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
John A. Crolla United Kingdom 38 2.9k 2.0k 1.2k 994 383 124 4.2k
Blake C. Ballif United States 36 3.2k 1.1× 1.8k 0.9× 1.3k 1.1× 776 0.8× 234 0.6× 75 4.0k
C Turleau France 36 2.6k 0.9× 2.1k 1.0× 1.0k 0.8× 781 0.8× 201 0.5× 160 4.0k
Ankita Patel United States 42 4.1k 1.4× 2.8k 1.4× 1.7k 1.3× 744 0.7× 324 0.8× 143 6.5k
Damien Sanlaville France 33 2.2k 0.8× 1.6k 0.8× 585 0.5× 385 0.4× 362 0.9× 189 3.7k
Dominique Smeets Netherlands 38 2.7k 0.9× 2.6k 1.3× 824 0.7× 776 0.8× 219 0.6× 112 4.9k
Robin M. Winter United Kingdom 30 3.5k 1.2× 2.9k 1.4× 554 0.4× 357 0.4× 228 0.6× 57 5.2k
Irene M. Janssen Netherlands 17 2.1k 0.7× 1.6k 0.8× 524 0.4× 522 0.5× 625 1.6× 23 3.4k
Weimin Bi United States 33 2.8k 1.0× 3.0k 1.5× 719 0.6× 528 0.5× 363 0.9× 92 5.5k
Thomy de Ravel Belgium 38 1.9k 0.7× 2.0k 1.0× 720 0.6× 250 0.3× 387 1.0× 112 4.2k
Giorgio Gimelli Italy 27 1.9k 0.6× 1.7k 0.9× 495 0.4× 949 1.0× 151 0.4× 128 3.4k

Countries citing papers authored by John A. Crolla

Since Specialization
Citations

This map shows the geographic impact of John A. 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 A. 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 A. Crolla more than expected).

Fields of papers citing papers by John A. Crolla

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of John A. Crolla

This figure shows the co-authorship network connecting the top 25 collaborators of John A. Crolla. A scholar is included among the top collaborators of John A. Crolla 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 John A. Crolla. John A. Crolla 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
1.
Barber, John, Jill A. Rosenfeld, Nicola Foulds, et al.. (2013). 8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients. American Journal of Medical Genetics Part A. 161(3). 487–500. 33 indexed citations
2.
3.
Alatzoglou, Kyriaki S., Cynthia L. Andoniadou, Daniel Kelberman, et al.. (2011). SOX2 haploinsufficiency is associated with slow progressing hypothalamo‐pituitary tumours. Human Mutation. 32(12). 1376–1380. 33 indexed citations
4.
Alberry, Medhat, et al.. (2011). Pseudotail as a feature of microphthalmia with linear skin defects syndrome. Clinical Dysmorphology. 20(2). 111–113. 4 indexed citations
5.
Robinson, David, et al.. (2008). Genetic analysis of chromosome 11p13 and the PAX6 gene in a series of 125 cases referred with aniridia. American Journal of Medical Genetics Part A. 146A(5). 558–569. 95 indexed citations
6.
Manoukian, Siranoush, John A. Crolla, M. Testi, et al.. (2005). Bilateral preaxial polydactyly in a WAGR syndrome patient. American Journal of Medical Genetics Part A. 134A(4). 426–429. 4 indexed citations
7.
Youings, Sheila, Nicholas R. Dennis, David S. Baldwin, et al.. (2003). Failure to Find DUP25 in Patients with Anxiety Disorders, in Control Individuals, or in Previously Reported Positive Control Cell Lines. The American Journal of Human Genetics. 72(3). 535–538. 38 indexed citations
8.
Cockwell, Annette E., Patricia A. Jacobs, Sarah J. Beal, & John A. Crolla. (2003). A study of cryptic terminal chromosome rearrangements in recurrent miscarriage couples detects unsuspected acrocentric pericentromeric abnormalities. Human Genetics. 112(3). 298–302. 28 indexed citations
9.
Crolla, John A. & Veronica van Heyningen. (2002). Frequent Chromosome Aberrations Revealed by Molecular Cytogenetic Studies in Patients with Aniridia. The American Journal of Human Genetics. 71(5). 1138–1149. 128 indexed citations
10.
Rivera, Horacio, Lina S. Correa-Cerro, David Robinson, & John A. Crolla. (2000). Functional Xp Disomy and Hypomelanosis of Ito. Archives of Medical Research. 31(1). 88–92. 4 indexed citations
11.
Hatchwell, Eli, et al.. (1998). Molecular confirmation of germ line mosaicism for a submicroscopic deletion of chromosome 22q11. American Journal of Medical Genetics. 78(2). 103–106. 23 indexed citations
12.
Fisher, Andrew, Annette E. Cockwell, N. Gregson, et al.. (1996). RAPIDIN SITU HARVESTING AND CYTOGENETIC ANALYSIS OF PERINATAL TISSUE SAMPLES. Prenatal Diagnosis. 16(7). 615–621. 11 indexed citations
13.
Huang, Binquan, John A. Crolla, Susan L. Christian, et al.. (1996). Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes. Human Genetics. 99(1). 11–17. 82 indexed citations
14.
MacPherson, John, John A. Crolla, N R Dennis, et al.. (1995). Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndrome.. Journal of Medical Genetics. 32(3). 236–239. 21 indexed citations
15.
Sugarman, Ian, John A. Crolla, & P.S. Malone. (1994). Mixed gonadal dysgenesis and cell line differentiation. Case presentation and literature review. Clinical Genetics. 46(4). 313–315. 17 indexed citations
16.
James, R S, et al.. (1994). Paternal isodisomy of chromosome 6 in association with a maternal supernumerary marker chromosome (6). The American Journal of Human Genetics. 55(7). 469–70. 2 indexed citations
17.
Fisher, Andrew, John Barber, John A. Crolla, et al.. (1993). Mosaic tetrasomy 8p: Molecular cytogenetic confirmation and measurement of glutathione reductase and tissue plasminogen activator levels. American Journal of Medical Genetics. 47(1). 100–105. 13 indexed citations
18.
Jacobs, P. A., P R Betts, Annette E. Cockwell, et al.. (1990). A cytogenetic and molecular reappraisal of a series of patients with Turner's syndrome. Annals of Human Genetics. 54(3). 209–223. 90 indexed citations
19.
Crolla, John A., S Gilgenkrantz, J. de Grouchy, Tadashi Kajii, & Martin Bobrow. (1989). Incontinentia pigmenti and X-autosome translocations. Human Genetics. 81(3). 269–272. 29 indexed citations
20.
Crolla, John A. & Juan Clinton Llerena. (1988). A mosaic 45,X/46,X,4(?) karyotype investigated with X and Y centromere-specific probes using a non-autoradiographic in situ hybridization technique. Human Genetics. 81(1). 81–84. 39 indexed citations

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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