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2. Sarcomas developed in patients with Lynch Syndrome are enriched in pleomorphic soft-tissue sarcomas and are sensitive to immunotherapy

4. Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

5. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

6. Diagnostic Yield of Chromosomal Microarray Analysis in Fetuses With Isolated Increased Nuchal Translucency: A French Multicenter Study

10. Effects of eight neuropsychiatric copy number variants on human brain structure

13. A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndrome

18. A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes

21. The enrichment of breakpoints in late-replicating chromatin provides novel insights into chromoanagenesis mechanisms

22. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

23. Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature Communications, (2021), 12, 1, (1078), 10.1038/s41467-020-20496-3).

24. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.

30. Whole Genome Sequencing of 9 patients allowed a better understanding of complex chromosomal rearrangements

31. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

32. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer.

33. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer.

34. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

35. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

36. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

37. Characterization of the diffusion properties of different gadolinium-based MRI contrast agents after ultrasound induced blood–brain barrier permeabilization

38. Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study

39. Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

40. Apport de l’ACPA dans le diagnostic étiologique des fœtus avec hyperclarté nucale au premier trimestre de grossesse : étude rétrospective multicentrique nationale incluant 720 fœtus

42. New insight in ARX-mutated patients' language specific impairment and underlying FOXP1 dysregulation

43. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

45. The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity

46. Xq28 duplication includingMECP2in six unreported affected females: what can we learn for diagnosis and genetic counselling?

48. Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders

49. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

50. Genetic analysis of 'PAX6-negative' individuals with aniridia or Gillespie Syndrome

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