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6. Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores.

7. Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

10. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

11. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

12. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

13. Association of genomic domains in BRCA1 and BRCA2 with prostate cancer risk and aggressiveness.

14. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.

15. Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D

16. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

17. Rare heterozygous DHTKD1 variants in patients with amyotrophic lateral sclerosis

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

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

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

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

25. Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification.

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

27. Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

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

29. Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

31. Konsensusempfehlung des Deutschen Konsortiums Familiärer Brust- und Eierstockkrebs zur Integration von Daten aus Multigenanalysen in das klinische Versorgungsprogramm

32. Truncating variants in DNA-repair genes and their effect on AAO of hereditary breast cancer

33. Rare compound heterozygous variants in PNKP identified by whole exome sequencing in a German patient with ataxia-oculomotor apraxia 4 and pilocytic astrocytoma

35. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

36. Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes

39. Benchmarking whole exome sequencing in the German network for personalized medicine.

40. Immunohistochemical marker profiles for the differentiation of collagenous spherulosis from adenoid cystic carcinoma of the breast.

41. Current genetic diagnostics in inborn errors of immunity.

42. Germline variants in patients developing second malignant neoplasms after therapy for pediatric acute lymphoblastic leukemia-a case-control study.

43. Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma families.

44. Ciliary Ultrastructure Assessed by Transmission Electron Microscopy in Adults with Bronchiectasis and Suspected Primary Ciliary Dyskinesia but Inconclusive Genotype.

45. Variants in FGF10 cause early onset of severe childhood interstitial lung disease: A detailed description of four affected children.

46. Prevalence of pericardial effusion in autosomal dominant polycystic kidney disease.

47. Parallel deletion and duplication at 7q11.23 in a silent carrier for two reciprocal syndromic disorders.

48. Diagnostic genomic sequencing in critically ill children.

49. Creation of a structured molecular genomics report for Germany as a local adaption of HL7's Genomic Reporting Implementation Guide.

50. A holistic approach to maximise diagnostic output in trio exome sequencing.

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