Mine Koprulu

Mine Koprulu

University of Cambridge

H-index: 8

Europe-United Kingdom

About Mine Koprulu

Mine Koprulu, With an exceptional h-index of 8 and a recent h-index of 8 (since 2020), a distinguished researcher at University of Cambridge, specializes in the field of Genomic medicine.

His recent articles reflect a diverse array of research interests and contributions to the field:

Identifying therapeutic targets for cancer among 2074 circulating proteins and risk of nine cancers

Similar and different: systematic investigation of proteogenomic variation between sexes and its relevance for human diseases

Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism

Proteogenomic links to human metabolic diseases

Genetic architecture and shared mechanisms of common′ neglected′ diseases

Identifying therapeutic targets for cancer: 2,094 circulating proteins and risk of nine cancers

Identifying proteomic risk factors for overall, aggressive and early onset prostate cancer using Mendelian randomization and tumor spatial transcriptomics

KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies

Mine Koprulu Information

University

Position

MRC Epidemiology Unit

Citations(all)

749

Citations(since 2020)

745

Cited By

114

hIndex(all)

8

hIndex(since 2020)

8

i10Index(all)

8

i10Index(since 2020)

8

Email

University Profile Page

Google Scholar

Mine Koprulu Skills & Research Interests

Genomic medicine

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
Maik Pietzner

H-Index: 21

Mine Koprulu
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
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

Cross-platform proteomics to advance genetic prioritisation strategies

BioRxiv

2021/3/19

Maik Pietzner
Maik Pietzner

H-Index: 21

Mine Koprulu
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
Mine Koprulu

H-Index: 1

Muhammad Shuaib
Muhammad Shuaib

H-Index: 9

See List of Professors in Mine Koprulu University(University of Cambridge)