P Jalbert
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 25
- Genomic variations and chromosomal abnormalities 16
- Chronic Lymphocytic Leukemia Research 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
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- Prenatal Screening and Diagnostics 8
- Co-authors
- B Sèle (11 shared papers)H Jalbert (7 shared papers)Marie‐Antoinette Voelckel (2 shared papers)Jean‐Louis Mandel (2 shared papers)Celia D. DeLozier-Blanchet (2 shared papers)Valérie Biancalana (2 shared papers)Joëlle Boué (2 shared papers)Isabelle Oberlé (2 shared papers)
In The Last Decade
P Jalbert
48 papers receiving 1.7k citations
P Jalbert's Hit Papers
Peers
Comparison fields: 5 of 76
- Genetics 1.3k
- Pediatrics, Perinatology and Child Health 416
- Cognitive Neuroscience 340
- Genetics 154
- Reproductive Medicine 110
Countries citing papers authored by P Jalbert
This map shows the geographic impact of P Jalbert'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 P Jalbert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P Jalbert more than expected).
Fields of papers citing papers by P Jalbert
This network shows the impact of papers produced by P Jalbert. 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 P Jalbert. The network helps show where P Jalbert may publish in the future.
Co-authors
The 25 scholars most cited alongside P Jalbert, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation Hit paper breakdown → | 1991 | 577 |
| 2 | 1980 | 168 | |
| 3 | 1991 | 151 | |
| 4 | 1983 | 137 | |
| 5 | 1986 | 101 | |
| 6 | 1992 | 83 | |
| 7 | 1975 | 68 | |
| 8 | 1994 | 63 | |
| 9 | 1995 | 60 | |
| 10 | 1979 | 51 | |
| 11 | 1993 | 47 | |
| 12 | 1996 | 45 | |
| 13 | 1997 | 43 | |
| 14 | 1990 | 43 | |
| 15 | Direct segregation analysis of reciprocal translocations: a study of 283 sperm karyotypes from four carriers. | 1989 | 41 |
| 16 | 1996 | 31 | |
| 17 | 1982 | 27 | |
| 18 | Structural genes of coagulation factors VII and X located on 13q34. | 1986 | 25 |
| 19 | 1989 | 25 | |
| 20 | 1993 | 21 |
About P Jalbert
P Jalbert is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology and Pathology and Forensic Medicine, having authored 50 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (8 papers), Lymphoma Diagnosis and Treatment (5 papers), Chromosomal and Genetic Variations (5 papers), DNA Repair Mechanisms (5 papers), Chronic Lymphocytic Leukemia Research (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Congenital heart defects research (4 papers). The work is most often cited by research in Genetics (1.3k citations), Pediatrics, Perinatology and Child Health (416 citations), Cognitive Neuroscience (340 citations), Genetics (154 citations) and Reproductive Medicine (110 citations). P Jalbert has collaborated with scholars based in France, Canada and Denmark. Frequent co-authors include B Sèle, H Jalbert, Marie‐Antoinette Voelckel, Jean‐Louis Mandel, Celia D. DeLozier-Blanchet, Valérie Biancalana, Joëlle Boué, Isabelle Oberlé, Dominique Heitz and Niels Tommerup. Their work appears in journals such as Human Genetics, British Journal of Haematology, Journal of Medical Genetics, European Journal of Obstetrics & Gynecology and Reproductive Biology and Obstetrical & Gynecological Survey.
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.