Leslie J. Jocelyn

555 total citations
7 papers, 408 citations indexed

About

Leslie J. Jocelyn is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Leslie J. Jocelyn has authored 7 papers receiving a total of 408 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Leslie J. Jocelyn's work include Genetics and Neurodevelopmental Disorders (2 papers), Congenital heart defects research (2 papers) and Autism Spectrum Disorder Research (2 papers). Leslie J. Jocelyn is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Congenital heart defects research (2 papers) and Autism Spectrum Disorder Research (2 papers). Leslie J. Jocelyn collaborates with scholars based in Canada, United States and Qatar. Leslie J. Jocelyn's co-authors include H. Rode, Albert E. Chudley, Bernard N. Chodirker, Oscar Casiro, Asuri N. Prasad, Christine Lee, Chitra Prasad and C. Prasad and has published in prestigious journals such as PEDIATRICS, Genetics in Medicine and Journal of Developmental & Behavioral Pediatrics.

In The Last Decade

Leslie J. Jocelyn

7 papers receiving 387 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Leslie J. Jocelyn Canada	6	226	168	104	69	68	7	408
José Salomão Schwartzman Brazil	15	259 1.1×	319 1.9×	199 1.9×	75 1.1×	48 0.7×	57	590
J Turk United Kingdom	14	347 1.5×	333 2.0×	120 1.2×	142 2.1×	53 0.8×	20	601
Loretta Thomaidis Greece	14	205 0.9×	84 0.5×	47 0.5×	128 1.9×	22 0.3×	40	452
Jacob Wisbeck United States	8	290 1.3×	249 1.5×	62 0.6×	132 1.9×	27 0.4×	12	374
Katherine S. Davlantis United States	4	75 0.3×	182 1.1×	52 0.5×	47 0.7×	18 0.3×	4	295
Norma Morrison United Kingdom	15	180 0.8×	122 0.7×	363 3.5×	236 3.4×	16 0.2×	24	794
Masutomo Miyao Japan	13	51 0.2×	138 0.8×	34 0.3×	40 0.6×	28 0.4×	27	346
Cláudia Berlim de Mello Brazil	13	121 0.5×	109 0.6×	36 0.3×	65 0.9×	90 1.3×	51	384
A Voutilainen Finland	11	68 0.3×	138 0.8×	93 0.9×	42 0.6×	73 1.1×	63	365
Mili Mehta United States	6	181 0.8×	328 2.0×	27 0.3×	84 1.2×	13 0.2×	11	445

Countries citing papers authored by Leslie J. Jocelyn

Since Specialization

Citations

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

Fields of papers citing papers by Leslie J. Jocelyn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leslie J. Jocelyn. 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 Leslie J. Jocelyn. The network helps show where Leslie J. Jocelyn may publish in the future.

Co-authorship network of co-authors of Leslie J. Jocelyn

This figure shows the co-authorship network connecting the top 25 collaborators of Leslie J. Jocelyn. A scholar is included among the top collaborators of Leslie J. Jocelyn 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 Leslie J. Jocelyn. Leslie J. Jocelyn is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

1.

Prasad, Chitra, Asuri N. Prasad, Bernard N. Chodirker, et al.. (2000). Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype. Clinical Genetics. 57(2). 103–109. 69 indexed citations

2.

Prasad, C., et al.. (1999). 22q 13 Deletion Syndrome: A Genetic Basis For Neurobehavioral Disorders?. Genetics in Medicine. 1(2). 60–60. 2 indexed citations

3.

Jocelyn, Leslie J., et al.. (1998). Treatment of Children with Autism. Journal of Developmental & Behavioral Pediatrics. 19(5). 326–334. 102 indexed citations

4.

Chudley, Albert E., et al.. (1998). Outcomes of Genetic Evaluation in Children with Pervasive Developmental Disorder. Journal of Developmental & Behavioral Pediatrics. 19(5). 321–325. 49 indexed citations

5.

Jocelyn, Leslie J., et al.. (1996). Alloimmune Thrombocytopenia of the Newborn: Neurodevelopmental Sequelae. American Journal of Perinatology. 13(4). 211–215. 32 indexed citations

6.

Jocelyn, Leslie J., et al.. (1996). Cognition, Communication, and Hearing in Young Children With Cleft Lip and Palate and in Control Children: A Longitudinal Study. PEDIATRICS. 97(4). 529–534. 120 indexed citations

7.

Jocelyn, Leslie J.. (1992). Neurodevelopmental Outcome of Term Infants With Intraventricular Hemorrhage. Archives of Pediatrics and Adolescent Medicine. 146(2). 194–194. 34 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.

Explore authors with similar magnitude of impact