P Jalbert
- Genetics top 2%
- Genomic variations and chromosomal abnormalities 15
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Chronic Lymphocytic Leukemia Research 4
- Genetics and Neurodevelopmental Disorders 4
- Cognitive Neuroscience top 5%
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- Prenatal Screening and Diagnostics 8
- Reproductive Medicine top 5%
- Genetics top 10%
- Genomic variations and chromosomal abnormalities 15
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Chronic Lymphocytic Leukemia Research 4
- Genetics and Neurodevelopmental Disorders 4
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- Chromosomal and Genetic Variations 6
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- DNA Repair Mechanisms 5
- Sexual Differentiation and Disorders 4
P Jalbert
58 papers receiving 1.6k citations
Hit Papers
Peers
Comparison fields: 5 of 73
- Genetics 1.1k
- Cognitive Neuroscience 368
- Pediatrics, Perinatology and Child Health 360
- Reproductive Medicine 118
- Genetics 135
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 37 | |
| 2 | 1996 | 30 | |
| 3 | 1996 | 37 | |
| 4 | 1996 | 9 | |
| 5 | 1995 | 58 | |
| 6 | 1994 | 0 | |
| 7 | 1994 | 47 | |
| 8 | 1993 | 21 | |
| 9 | 1993 | 33 | |
| 10 | 1992 | 65 | |
| 11 | 1991 | 139 | |
| 12 | Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardationbreakdown → | 1991 | 540 |
| 13 | 1990 | 44 | |
| 14 | Direct segregation analysis of reciprocal translocations: a study of 283 sperm karyotypes from four carriers. | 1989 | 39 |
| 15 | [Induction of sister chromatide exchange by trichloroethylene and its metabolites (author's transl)]. | 1981 | 5 |
| 16 | 1979 | 6 | |
| 17 | 1979 | 47 | |
| 18 | [Ring 6-chromosome: a nonspecific clinical picture]. | 1977 | 9 |
| 19 | [Ring chromosome 14 in monozygotic twins]. | 1977 | 9 |
| 20 | [Hallermann-Streiff-François syndrome: a recent case associated with a karyotypic 4 p-anomaly]. | 1968 | 13 |
About P Jalbert
P Jalbert is a scholar working on Genetics, Reproductive Medicine, Pediatrics, Perinatology and Child Health, Developmental Biology and Genetics, having authored 59 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (8 papers), Chromosomal and Genetic Variations (6 papers), DNA Repair Mechanisms (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Chronic Lymphocytic Leukemia Research (4 papers), Sexual Differentiation and Disorders (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). The work is most often cited by research in Genetics (1.1k citations), Cognitive Neuroscience (368 citations), Pediatrics, Perinatology and Child Health (360 citations), Reproductive Medicine (118 citations) and Genetics (135 citations). P Jalbert has collaborated with scholars based in France, Denmark and Canada. Frequent co-authors include B Sèle, H Jalbert, Joëlle Boué, Marie‐Antoinette Voelckel, Jean‐Louis Mandel, Dominique Heitz, Christine Kretz, Valérie Biancalana, Niels Tommerup and I. Oberlé. Their work appears in journals such as Human Genetics, British Journal of Haematology, Journal of Medical Genetics, Human Reproduction 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.