Karim Oualkacha

The UK10K project identifies rare variants in health and disease

Josine L. Min, Jie Huang, Yasin Memari et al. · Nature · 2015 · 1.2K citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

Jie Huang, Bryan Howie, Shane McCarthy et al. · Nature Communications · 2015 · 385 citations · Full text

Public Health, Genetics, Molecular Genetics +17

The UK10K project identifies rare variants in health and disease

Klaudia Walter, Josine L. Min, Jie Huang et al. · Kölner Universitäts PublikationsServer (Universität zu Köln) · 2015 · 299 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

Miriam Schmidts, Yuqing Hou, Claudio R. Cortés et al. · Nature Communications · 2015 · 84 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

Nicholas J. Timpson, Klaudia Walter, Josine L. Min et al. · Nature Communications · 2014 · 74 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16