L.E. Bernard

510 total citations
10 papers, 376 citations indexed

About

L.E. Bernard is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, L.E. Bernard has authored 10 papers receiving a total of 376 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 4 papers in Pediatrics, Perinatology and Child Health and 3 papers in Molecular Biology. Recurrent topics in L.E. Bernard's work include Genetic Syndromes and Imprinting (5 papers), Prenatal Screening and Diagnostics (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). L.E. Bernard is often cited by papers focused on Genetic Syndromes and Imprinting (5 papers), Prenatal Screening and Diagnostics (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). L.E. Bernard collaborates with scholars based in Canada and United States. L.E. Bernard's co-authors include Sylvie Langlois, Wendy P. Robinson, Dagmar K. Kalousek, Irene Barrett, R. Douglas Wilson, Adèle Telenius, P. N. Howard‐Peebles, Robert G. Best, Fosco Bernasconi and Éric Gagné and has published in prestigious journals such as Genomics, Journal of Medical Genetics and Human Mutation.

In The Last Decade

L.E. Bernard

10 papers receiving 368 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
L.E. Bernard Canada	7	294	289	150	31	28	10	376
Lukas Soellner Germany	12	480 1.6×	348 1.2×	356 2.4×	58 1.9×	24 0.9×	22	609
Jia‐Chi Wang Canada	12	234 0.8×	196 0.7×	118 0.8×	21 0.7×	5 0.2×	28	385
Anne‐Marie Lind Denmark	9	257 0.9×	190 0.7×	141 0.9×	27 0.9×	11 0.4×	10	360
Michiko Ohno Japan	8	142 0.5×	134 0.5×	113 0.8×	61 2.0×	7 0.3×	14	383
Lucy Bowden United Kingdom	6	440 1.5×	273 0.9×	562 3.7×	85 2.7×	11 0.4×	9	647
Nadine Schönherr Germany	8	350 1.2×	258 0.9×	299 2.0×	15 0.5×	8 0.3×	14	398
A. Bou� France	9	155 0.5×	122 0.4×	134 0.9×	44 1.4×	6 0.2×	11	388
Frédérique Tihy Canada	11	215 0.7×	146 0.5×	120 0.8×	16 0.5×	8 0.3×	18	384
Alexandra Spadola United States	2	180 0.6×	77 0.3×	290 1.9×	17 0.5×	11 0.4×	3	348
Eva Pompilii Italy	7	145 0.5×	245 0.8×	50 0.3×	32 1.0×	12 0.4×	13	298

Countries citing papers authored by L.E. Bernard

Since Specialization

Citations

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

Fields of papers citing papers by L.E. Bernard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by L.E. Bernard. 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 L.E. Bernard. The network helps show where L.E. Bernard may publish in the future.

Co-authorship network of co-authors of L.E. Bernard

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

All Works

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10 of 10 papers shown

Vallance, Hilary, et al.. (1999). Identification of 6 new mutations in the iduronate sulfatase gene. Human Mutation. 13(4). 338–338. 5 indexed citations

Bernard, L.E., et al.. (1999). Duty to Re‐Contact: A Study of Families at Risk for Fragile X. Journal of Genetic Counseling. 8(1). 3–15. 8 indexed citations

Bernard, L.E., et al.. (1999). Clinical and molecular findings in two patients with Russell-Silver syndrome and UPD7: Comparison with non-UPD7 cases. American Journal of Medical Genetics. 87(3). 230–236. 37 indexed citations

Robinson, Wendy P., Irene Barrett, L.E. Bernard, et al.. (1997). Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction.. PubMed. 60(4). 917–27. 164 indexed citations

Hansen, Wendy, L.E. Bernard, Sylvie Langlois, et al.. (1997). MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME 2 AND CONFINED PLACENTAL MOSAICISM FOR TRISOMY 2 IN A FETUS WITH INTRAUTERINE GROWTH RESTRICTION, HYPOSPADIAS, AND OLIGOHYDRAMNIOS. Prenatal Diagnosis. 17(5). 443–450. 50 indexed citations

Kalousek, Dagmar K., Sylvie Langlois, Wendy P. Robinson, et al.. (1996). Trisomy 7 CVS mosaicism: Pregnancy outcome, placental and DNA analysis in 14 cases. American Journal of Medical Genetics. 65(4). 348–352. 46 indexed citations

Bernard, L.E., David Chitayat, Rosanna Weksberg, M. I. Van Allen, & Sylvie Langlois. (1996). Linkage analysis of two Canadian families segregating for X linked spondyloepiphyseal dysplasia.. Journal of Medical Genetics. 33(5). 432–434. 6 indexed citations

Benlian, Pascale, L. Foubert, Éric Gagné, et al.. (1996). Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiency.. PubMed. 59(2). 431–6. 45 indexed citations

Bernard, L.E. & Stephen Wood. (1993). Human chromosome 5 sequence primer amplifies Alu polymorphisms on chromosomes 2 and 17. Genome. 36(2). 302–309. 2 indexed citations

10.

Bernard, L.E., Angela Brooks‐Wilson, & Stephen Wood. (1991). Isolation of DNA fragments from a human chromosomal subregion by Alu PCR differential hybridization. Genomics. 9(2). 241–246. 13 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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