David Chitayat

5.2k total citations
61 papers, 1.7k citations indexed

About

David Chitayat is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, David Chitayat has authored 61 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 21 papers in Genetics and 16 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in David Chitayat's work include Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (10 papers) and Congenital heart defects research (6 papers). David Chitayat is often cited by papers focused on Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (10 papers) and Congenital heart defects research (6 papers). David Chitayat collaborates with scholars based in Canada, United States and Israel. David Chitayat's co-authors include Gideon Koren, Andrea Gaedigk, James Cairns, Steven J. Leeder, Dorothy Warburton, James J. Russo, Stephen Brown, Rosa Ferrentino, Germana Meroni and Hugh OʼBrodovich and has published in prestigious journals such as The Lancet, Circulation and SHILAP Revista de lepidopterología.

In The Last Decade

David Chitayat

56 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Chitayat Canada 22 632 530 438 235 202 61 1.7k
Sara Hamon United States 29 681 1.1× 248 0.5× 151 0.3× 447 1.9× 82 0.4× 71 2.3k
K Nahoul France 22 475 0.8× 276 0.5× 135 0.3× 165 0.7× 32 0.2× 66 2.1k
Ian N. M. Day United Kingdom 16 478 0.8× 304 0.6× 94 0.2× 138 0.6× 82 0.4× 25 1.7k
Jennifer R. King United States 19 460 0.7× 211 0.4× 433 1.0× 99 0.4× 67 0.3× 61 1.9k
Andrew E. Mulberg United States 25 364 0.6× 299 0.6× 236 0.5× 417 1.8× 32 0.2× 74 1.7k
Ursula Kuhnle Germany 26 1.2k 1.9× 512 1.0× 139 0.3× 186 0.8× 27 0.1× 78 1.8k
Michela Rebsamen Switzerland 13 297 0.5× 132 0.2× 76 0.2× 108 0.5× 46 0.2× 16 1.3k
Keita Harada Japan 22 425 0.7× 400 0.8× 149 0.3× 565 2.4× 27 0.1× 139 1.9k
Nora V. Bergasa United States 32 292 0.5× 140 0.3× 165 0.4× 905 3.9× 554 2.7× 96 4.2k
Christoph Baerwald Germany 27 527 0.8× 147 0.3× 82 0.2× 86 0.4× 42 0.2× 134 2.3k

Countries citing papers authored by David Chitayat

Since Specialization
Citations

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

Fields of papers citing papers by David Chitayat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Chitayat

This figure shows the co-authorship network connecting the top 25 collaborators of David Chitayat. A scholar is included among the top collaborators of David Chitayat 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 David Chitayat. David Chitayat 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.
Miller, Elka, Kamini Raghuram, Patrick Shannon, et al.. (2024). Associations and outcomes of prenatally detected rhombencephalosynapsis. Prenatal Diagnosis. 44(10). 1159–1169.
2.
Ashwal‏, Eran, Susan Blasér, Pradeep Krishnan, et al.. (2023). Anterior extension of the choroid plexus into the frontal horns of the fetal lateral cerebral ventricles: Prenatal findings and postnatal outcome. Prenatal Diagnosis. 43(6). 756–762. 1 indexed citations
3.
Wang, Yiming, et al.. (2023). Role of comprehensive cytogenomic investigation in successful reproductive outcome of parental small neocentromeric supernumerary ring chromosome: A case report. SHILAP Revista de lepidopterología. 11(4). e6632–e6632. 2 indexed citations
4.
Mendoza‐Londono, Roberto, David Chitayat, Walter H.A. Kahr, et al.. (2012). Extracellular matrix and platelet function in patients with musculocontractural Ehlers–Danlos syndrome caused by mutations in theCHST14gene. American Journal of Medical Genetics Part A. 158A(6). 1344–1354. 25 indexed citations
5.
Madadi, Parvaz, et al.. (2011). Genetic Transmission of Cytochrome P450 2D6 (CYP2D6) Ultrarapid Metabolism: Implications for Breastfeeding Women taking Codeine. Current Drug Safety. 6(1). 36–39. 21 indexed citations
6.
Hartley, Jane, Nicholas C. Zachos, Ban B. Dawood, et al.. (2010). Mutations in TTC37 Cause Trichohepatoenteric Syndrome (Phenotypic Diarrhea of Infancy). Gastroenterology. 138(7). 2388–2398.e2. 96 indexed citations
7.
Cameron, Jessie M., Valeriy Levandovskiy, Nevena MacKay, et al.. (2010). Complex V TMEM70 deficiency results in mitochondrial nucleoid disorganization. Mitochondrion. 11(1). 191–199. 35 indexed citations
8.
Chitayat, David, et al.. (2009). Long-term functional results following resection of neonatal sacrococcygeal teratoma. Pediatric Surgery International. 25(3). 243–246. 33 indexed citations
9.
Chitayat, David, et al.. (2009). Combined immunodeficiency, facial dysmorphism, optic nerve atrophy, skeletal anomalies and developmental delay: a new syndrome. Clinical Genetics. 76(5). 449–457. 5 indexed citations
10.
Mari, Francesca, Brunella Franco, Alessandra Renieri, et al.. (2008). Disruption of the IQSEC2 transcript in a female with X;autosome translocation t(X;20)(p11.2;q11.2) and a phenotype resembling X-linked infantile spasms (ISSX) syndrome. Molecular Medicine Reports. 1(1). 33–9. 18 indexed citations
11.
Nicolaou, Paschalis, et al.. (2006). A Novel GDAP1 Mutation 439delA is Associated with Autosomal Recessive CMT Disease. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 33(3). 311–316. 6 indexed citations
12.
Koren, Gideon, James Cairns, David Chitayat, Andrea Gaedigk, & Steven J. Leeder. (2006). Pharmacogenetics of morphine poisoning in a breastfed neonate of a codeine-prescribed mother. The Lancet. 368(9536). 704–704. 424 indexed citations
13.
Falco, Francesca De, Silvia Cainarca, Grazia Andolfi, et al.. (2003). X‐linked Opitz syndrome: Novel mutations in the MID1 gene and redefinition of the clinical spectrum. American Journal of Medical Genetics Part A. 120A(2). 222–228. 72 indexed citations
14.
Barréa, Catherine, Shi‐Joon Yoo, David Chitayat, et al.. (2002). Assessment of the thymus at echocardiography in fetuses at risk for 22q11.2 deletion. Prenatal Diagnosis. 23(1). 9–15. 20 indexed citations
15.
Koren, Gideon, Tony Cohn, David Chitayat, et al.. (2002). Use of Atypical Antipsychotics During Pregnancy and the Risk of Neural Tube Defects in Infants. American Journal of Psychiatry. 159(1). 136–137. 45 indexed citations
16.
Vajsar, Jiri, Cameron Ackerley, David Chitayat, & Laurence E. Becker. (2000). Basal lamina abnormality in the skeletal muscle of Walker-Warburg syndrome. Pediatric Neurology. 22(2). 139–143. 15 indexed citations
17.
Arab, Sara, et al.. (1999). Mosaicism for a small marker chromosome resulting from a familial Robertsonian translocation (21;22). Clinical Genetics. 56(5). 363–367. 1 indexed citations
18.
Tizzano, Eduardo F., et al.. (1994). Regional Expression of CFTR in Developing Human Respiratory Tissues. American Journal of Respiratory Cell and Molecular Biology. 10(4). 355–362. 55 indexed citations
19.
Chitayat, David, et al.. (1988). Cold-induced abortion in paramyotonia congenita. American Journal of Obstetrics and Gynecology. 158(2). 435–436. 11 indexed citations
20.
Chitayat, David, Sachiko Nakagawa, Robert W. Marion, et al.. (1988). Aspartylglucosaminuria in a Puerto Rican family: Additional features of a panethnic disorder. American Journal of Medical Genetics. 31(3). 527–532. 11 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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