L.E. Bernard
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 10%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 8
- Genetic Syndromes and Imprinting 5
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 1
-
- Prenatal Screening and Diagnostics 4
- Co-authors
- Sylvie Langlois (6 shared papers)Wendy P. Robinson (5 shared papers)Irene Barrett (3 shared papers)Dagmar K. Kalousek (3 shared papers)Adèle Telenius (2 shared papers)P. N. Howard‐Peebles (2 shared papers)R. Douglas Wilson (2 shared papers)Robert G. Best (1 shared paper)
- Journals
- Prenatal Diagnosis (1 paper)Genomics (1 paper)Journal of Medical Genetics (1 paper)Genome (1 paper)Human Mutation (1 paper)
- Partner nations
- CanadaUnited States
In The Last Decade
L.E. Bernard
10 papers receiving 367 citations
Peers
Comparison fields: 5 of 37
- Pediatrics, Perinatology and Child Health 254
- Genetics 246
- Obstetrics and Gynecology 17
- Molecular Biology 130
- Genetics 8
Countries citing papers authored by L.E. Bernard
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
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-authors
The 25 scholars most cited alongside L.E. Bernard, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 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. | 1997 | 164 |
| 2 | 1997 | 50 | |
| 3 | 1996 | 46 | |
| 4 | Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiency. | 1996 | 45 |
| 5 | 1999 | 35 | |
| 6 | 1991 | 13 | |
| 7 | 1999 | 8 | |
| 8 | 1996 | 6 | |
| 9 | 1999 | 5 | |
| 10 | 1993 | 2 |
About L.E. Bernard
L.E. Bernard is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Plant Science and Surgery, having authored 10 papers that have together received 374 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (5 papers), Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Chromosomal and Genetic Variations (2 papers), Autism Spectrum Disorder Research (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Trypanosoma species research and implications (1 paper) and Biomedical Research and Pathophysiology (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (254 citations), Genetics (246 citations), Obstetrics and Gynecology (17 citations), Molecular Biology (130 citations) and Genetics (8 citations). L.E. Bernard has collaborated with scholars based in Canada and United States. Frequent co-authors include Sylvie Langlois, Wendy P. Robinson, Irene Barrett, Dagmar K. Kalousek, Adèle Telenius, P. N. Howard‐Peebles, R. Douglas Wilson, Robert G. Best, Fosco Bernasconi and L. Foubert. Their work appears in journals such as Prenatal Diagnosis, Genomics, Journal of Medical Genetics, Genome and Human Mutation.
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.