Mine Koprulu
University of Cambridge
H-index: 8
Europe-United Kingdom
Top articles of Mine Koprulu
Identifying therapeutic targets for cancer among 2074 circulating proteins and risk of nine cancers
Nature Communications
2024/4/29
Similar and different: systematic investigation of proteogenomic variation between sexes and its relevance for human diseases
medRxiv
2024
Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism
nature communications
2023/6/7
Proteogenomic links to human metabolic diseases
Nature metabolism
2023/3
Genetic architecture and shared mechanisms of common′ neglected′ diseases
medRxiv
2023
Identifying therapeutic targets for cancer: 2,094 circulating proteins and risk of nine cancers
medRxiv
2023
Identifying proteomic risk factors for overall, aggressive and early onset prostate cancer using Mendelian randomization and tumor spatial transcriptomics
medRxiv
2023/9/22
KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
European Journal of Human Genetics
2022/11
Detection and characterization of male sex chromosome abnormalities in the UK Biobank study
Genetics in medicine
2022/9/1
From genome to phenome via the proteome: broad capture, antibody-based proteomics to explore disease mechanisms
medRxiv
2022/8/22
Trans-ancestry meta-analysis improves performance of genetic scores for multiple adiposity-related traits in East Asian populations
2022/7/29
Identification of rare loss-of-function genetic variation regulating body fat distribution
The Journal of Clinical Endocrinology & Metabolism
2022/4/1
Synergistic insights into human health from aptamer-and antibody-based proteomic profiling
Nature communications
2021/11/24
Maik Pietzner
H-Index: 21
Mine Koprulu
H-Index: 1
Mapping the proteo-genomic convergence of human diseases
Science
2021/10/14
Identification of rare loss of function variation regulating body fat distribution
medRxiv
2021/9/15
GIGYF1 loss of function is associated with clonal mosaicism and adverse metabolic health
Nature Communications
2021/7/7
The first adolescent case of Fraser syndrome 3, with a novel nonsense variant in GRIP1
American Journal of Medical Genetics Part A
2021/6
Mine Koprulu
H-Index: 1
CRADD and USP44 mutations in intellectual disability, mild lissencephaly, brain atrophy, developmental delay, strabismus, behavioural problems and skeletal anomalies
European Journal of Medical Genetics
2021/4/1
Mine Koprulu
H-Index: 1
Rana Muhammad Kamran Shabbir
H-Index: 3
Qamar Zaman
H-Index: 3
Gökhan Nalbant
H-Index: 1
Cross-platform proteomics to advance genetic prioritisation strategies
BioRxiv
2021/3/19
Maik Pietzner
H-Index: 21
Mine Koprulu
H-Index: 1
Biallelic ZNF407 mutations in a neurodevelopmental disorder with ID, short stature and variable microcephaly, hypotonia, ocular anomalies and facial dysmorphism
Journal of Human Genetics
2020/12
Mine Koprulu
H-Index: 1
Muhammad Shuaib
H-Index: 9