Robert Klein

发表

Genome sequencing identifies major causes of severe intellectual disability

L. Vissers, A. Hoischen, R. Pfundt, 2014, Nature.

Comprehensive Genetic Landscape of Uveal Melanoma by Whole-Genome Sequencing.

Nicolò Riggi, G. Ciriello, C. Rivolta, 2016, American journal of human genetics.

Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine

Michael Brudno, Daniele Merico, Christian R Marshall, 2016, npj Genomic Medicine.

Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.

William Wheeler, Hideo Tanaka, Jianxin Shi, 2014, Human molecular genetics.

Characterization of large structural genetic mosaicism in human autosomes.

William Wheeler, Nan Hu, Peter Kraft, 2015, American journal of human genetics.

Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women.

Hongbing Shen, Chien-Jen Chen, N. Rothman, 2016, Human molecular genetics.

Premalignant SOX2 overexpression in the fallopian tubes of ovarian cancer patients: Discovery and validation studies

Rebecca Yu Zhang, C. Yau, G. McVean, 2016, EBioMedicine.

Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome

William Wheeler, Nan Hu, Peter Kraft, 2016, Nature Communications.

Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.

David M. Thomas, Krista A. Zanetti, Geoffrey S. Tobias, 2014, Human molecular genetics.

Characterization of large structural genetic mosaicism in human autosomes.

Krista A. Zanetti, Geoffrey S. Tobias, Sarah C. Nelson, 2015, American journal of human genetics.