Search

Your search keyword '"Brauch H."' showing total 964 results

Search Constraints

Start Over You searched for: Author "Brauch H." Remove constraint Author: "Brauch H."
964 results on '"Brauch H."'

Search Results

51. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

52. Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium

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

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

55. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

56. Two truncating variants in FANCC and breast cancer risk.

57. A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.

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

59. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk.

60. Transcriptome-wide association study of breast cancer risk by estrogen-receptor status.

61. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.

62. Obesity Alters Endoxifen Plasma Levels in Young Breast Cancer Patients: A Pharmacometric Simulation Approach

63. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

64. Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

65. Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.

66. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

67. A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

68. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

69. Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

70. A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

71. Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.

77. Shared heritability and functional enrichment across six solid cancers (vol 10, 431, 2019)

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

79. Two truncating variants in FANCC and breast cancer risk

80. Genome-wide association study of germline variants and breast cancer-specific mortality

81. Genome-wide association study of germline variants and breast cancer-specific mortality

82. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

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

84. Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis

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

90. Shared heritability and functional enrichment across six solid cancers.

91. Genome-wide association study of germline variants and breast cancer-specific mortality.

92. Publisher Correction: Shared heritability and functional enrichment across six solid cancers (Nature Communications, (2019), 10, 1, (431), 10.1038/s41467-018-08054-4).

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

94. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes.

95. Erratum: Publisher Correction: Shared heritability and functional enrichment across six solid cancers (Nature communications (2019) 10 1 (431))

96. Shared heritability and functional enrichment across six solid cancers

97. Two truncating variants in FANCC and breast cancer risk

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

99. Shared heritability and functional enrichment across six solid cancers (vol 10, 431, 2019)

100. Genome-wide association study of germline variants and breast cancer-specific mortality

Catalog

Books, media, physical & digital resources