Florent Diéterlen
Biographic Data
| ID | 4090705 |
|---|---|
| NAME | Florent Diéterlen |
| GIVEN NAMES | Florent |
| FAMILY NAME | Diéterlen |
| SIGNATURE | DIÉTERLEN F |
| AFFILIATIONS | Immunologie et Neurogénétique Expérimentales et Moléculaires |
| VERIFIED | No |
| TOTAL WORKS | 7 |
| TOTAL CITATIONS | 2 |
| WORKS AS AUTHOR | 7 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2006 |
| LATEST PUBLICATION YEAR | 2019 |
| H-INDEX | 1 |
The Y-SNP Z-381 Is a Patrilineal DNA Marker of the Royal Bourbon Family of France
More than 1100 unrelated males from West-Europe were analysed by molecular hybridization experiments for the p49, f Taq I polymorphisms, and by polymerase chain reaction for the R-S21 and Z381 Y-SNP markers. The corresponding two SNP haplogroups showed similar packty frequency distribution patterns centred on Belgium, the Netherlands, Denmark and the north of Germany. Louis XVI, the last French King, is Z381+. A complete corrected Y-STRs profile …
Original Synthetic Report
Background: The G2019S mutation in the LRRK2 gene is associated with 1-2% of sporadic Parkinson’s disease (PD) cases. In Europe, the prevalence of G2019S in sporadic PD patients depends on the population, being relatively high in Spain and Portugal but low in northern Europe. Aim: To drawn up a European frequency map of the G2019S mutation. Material and Methods: A map of G2019S mutation isofrequences in Europe has been drawn up using the Spatial …
Original Synthetic Report
Mutation 35delG in the connexin-26 gene is the main cause of recessive deafness in Europe. The aim of this study is to determine the percentage of carriers of this mutation in seven regions of the Greek-Turkish area; previous studies indicated that the prevalence of the mutation was relatively elevated in Greece. This study has been carried out on the genomic DNAs of a total of 1038 healthy subjects originating from Albania, Bulgaria, Athens (Gre…
Y-Chromosome Haplotypes in the Greek–Turkish Area
Various populations have contributed to the present-day gene pool in oriental Mediterranean (Aegean Sea) and are well documented for ancient history. The primary objective of the study is to report on the analysis of the paternal component of the variation (Y chromosome haplotypes) in contemporary populations in Greece, Crete, Turkey and Cyprus. A total of 245 males who hailed from five different locations in Turkey, Greece, and the islands of Cr…
Y-Haplotype X in the Balkans
A total of 2110 unrelated European male subjects were examined for the p49a,f TaqI Y-haplotype X. The results showed a remarkable mean peak of haplotype X frequencies (46.9%) among subjects from Croatia, and similar elevated frequency values were also found in their counterparts from Slovenia (41.5%), Bosnia (40.3%) and ex-Yugoslavia (36.7%). Frequencies of haplotype X decrease towards west (from 41.5% in Slovenia to less than 1% in northern Ital…
Characterization of the Y-Chromosome Sardinian–Corsican Haplotype
The Y chromosome of 523 Italian male subjects was examined for the 49a,f TaqI haplotype XII and for two microsatellites, YCAIIa and YCAIIb. Results were then compared to other populations living in the western Mediterranean basin whom we had previously studied: 419 French (including 328 Corsicans), 46 Italians from Milan, and 73 Tunisians. Haplotype XII is present in 127 out of the 1061 examined samples (11.9%), and most of the haplotype XII subj…
North African Berber and Arab Influences in the Western Mediterranean Revealed by Y-Chromosome DNA Haplotypes
We have analyzed Y-chromosome diversity in the western Mediterranean area, examining p49a,f TaqI haplotype V and subhaplotypes Vb (Berber) and Va (Arab). A total of 2,196 unrelated DNA samples, belonging to 22 populations from North Africa and the southern Mediterranean coast of occidental Europe, have been typed. Subhaplotype Vb, predominant in a Berber population of Morocco (63.5%), was also found at high frequencies in southern Portugal (35.9%…
North African Berber and Arab Influences in the Western Mediterranean Revealed by Y-Chromosome DNA Haplotypes
We have analyzed Y-chromosome diversity in the western Mediterranean area, examining p49a,f TaqI haplotype V and subhaplotypes Vb (Berber) and Va (Arab). A total of 2,196 unrelated DNA samples, belonging to 22 populations from North Africa and the southern Mediterranean coast of occidental Europe, have been typed. Subhaplotype Vb, predominant in a Berber population of Morocco (63.5%), was also found at high frequencies in southern Portugal (35.9%…
Y-Chromosome Haplotypes in the Greek–Turkish Area
Various populations have contributed to the present-day gene pool in oriental Mediterranean (Aegean Sea) and are well documented for ancient history. The primary objective of the study is to report on the analysis of the paternal component of the variation (Y chromosome haplotypes) in contemporary populations in Greece, Crete, Turkey and Cyprus. A total of 245 males who hailed from five different locations in Turkey, Greece, and the islands of Cr…
Y-Haplotype X in the Balkans
A total of 2110 unrelated European male subjects were examined for the p49a,f TaqI Y-haplotype X. The results showed a remarkable mean peak of haplotype X frequencies (46.9%) among subjects from Croatia, and similar elevated frequency values were also found in their counterparts from Slovenia (41.5%), Bosnia (40.3%) and ex-Yugoslavia (36.7%). Frequencies of haplotype X decrease towards west (from 41.5% in Slovenia to less than 1% in northern Ital…
Characterization of the Y-Chromosome Sardinian–Corsican Haplotype
The Y chromosome of 523 Italian male subjects was examined for the 49a,f TaqI haplotype XII and for two microsatellites, YCAIIa and YCAIIb. Results were then compared to other populations living in the western Mediterranean basin whom we had previously studied: 419 French (including 328 Corsicans), 46 Italians from Milan, and 73 Tunisians. Haplotype XII is present in 127 out of the 1061 examined samples (11.9%), and most of the haplotype XII subj…
North African Berber and Arab Influences in the Western Mediterranean Revealed by Y-Chromosome DNA Haplotypes
We have analyzed Y-chromosome diversity in the western Mediterranean area, examining p49a,f TaqI haplotype V and subhaplotypes Vb (Berber) and Va (Arab). A total of 2,196 unrelated DNA samples, belonging to 22 populations from North Africa and the southern Mediterranean coast of occidental Europe, have been typed. Subhaplotype Vb, predominant in a Berber population of Morocco (63.5%), was also found at high frequencies in southern Portugal (35.9%…
Original Synthetic Report
Background: The G2019S mutation in the LRRK2 gene is associated with 1-2% of sporadic Parkinson’s disease (PD) cases. In Europe, the prevalence of G2019S in sporadic PD patients depends on the population, being relatively high in Spain and Portugal but low in northern Europe. Aim: To drawn up a European frequency map of the G2019S mutation. Material and Methods: A map of G2019S mutation isofrequences in Europe has been drawn up using the Spatial …
Original Synthetic Report
Mutation 35delG in the connexin-26 gene is the main cause of recessive deafness in Europe. The aim of this study is to determine the percentage of carriers of this mutation in seven regions of the Greek-Turkish area; previous studies indicated that the prevalence of the mutation was relatively elevated in Greece. This study has been carried out on the genomic DNAs of a total of 1038 healthy subjects originating from Albania, Bulgaria, Athens (Gre…
The Y-SNP Z-381 Is a Patrilineal DNA Marker of the Royal Bourbon Family of France
More than 1100 unrelated males from West-Europe were analysed by molecular hybridization experiments for the p49, f Taq I polymorphisms, and by polymerase chain reaction for the R-S21 and Z381 Y-SNP markers. The corresponding two SNP haplogroups showed similar packty frequency distribution patterns centred on Belgium, the Netherlands, Denmark and the north of Germany. Louis XVI, the last French King, is Z381+. A complete corrected Y-STRs profile …
Biology (7 works) · Gene (7 works) · Genetics (7 works) · Genotype (7 works) · Geography (6 works) · Haplotype (6 works) · Demography (5 works) · Forensic and Genetic Research (5 works) · TaqI (4 works) · Genetics (3 works)