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111 |
Assessing the usefulness of a novel MRI-based breast density estimation algorithm in a cohort of women at high genetic risk of breast cancer: the UK MARIBS study
Enthalten in Breast cancer research Bd. 11, 11.11.2009, Nr. 6, date:12.2009: 1-16
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112 |
Assessment of long-term psychosocial outcomes in N-methyl-D-aspartate receptor encephalitis – the SAPIENCE study protocol
Enthalten in BMC neurology Bd. 24, 6.9.2024, Nr. 1, date:12.2024: 1-8
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113 |
Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy
Enthalten in Breast cancer research Bd. 17, 10.2.2015, Nr. 1, date:12.2015: 1-13
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114 |
Association analyses identify 31 new risk loci for colorectal cancer susceptibility
Enthalten in Nature Communications Bd. 10, 14.5.2019, Nr. 1, date:12.2019: 1-15
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115 |
Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment
Enthalten in Breast cancer research Bd. 23, 18.8.2021, Nr. 1, date:12.2021: 1-18
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116 |
Association of tamoxifen use and reduced risk of contralateral breast cancer for BRCA1 and BRCA2 mutation carriers
Enthalten in Hereditary cancer in clinical practice Bd. 10, 12.4.2012, Nr. 2, date:12.2012: 1-2
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117 |
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers
Enthalten in Breast cancer research Bd. 16, 31.12.2014, Nr. 6, date:12.2014: 1-27
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118 |
Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium
Enthalten in Breast cancer research Bd. 25, 20.6.2023, Nr. 1, date:12.2023: 1-13
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119 |
Audit of hemostatic clip use after colorectal polyp resection in an academic endoscopy unit
Enthalten in Endoscopy International Open Bd. 12, 2024, Nr. 04: E579-E584
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120 |
Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk
Enthalten in Nature genetics Bd. 55, 26.9.2023, Nr. 11, date:11.2023: 2009
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