Lili Li

Identification of gene fusion transcripts by transcriptome sequencing in BRCA1-mutated breast cancers and cell lines

A. Ashworth, W. Foulkes, J. Reis-Filho, 2011, BMC Medical Genomics.

A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotype

Michael J. McGuffin, S. Gruber, W. Foulkes, 2015, Journal of Medical Genetics.

A homozygous PMS 2 founder mutation with an attenuated constitutional mismatch repair de fi ciency phenotype

S. Gruber, W. Foulkes, R. Hegele, 2015 .

Analysis of PALB2/FANCN-associated breast cancer families

Petra M. Nederlof, Jorge S. Reis-Filho, David M. Livingston, 2007, Proceedings of the National Academy of Sciences.

Rare germline mutations in PALB2 and breast cancer risk: A population‐based study

C. Begg, W. Foulkes, S. Tavtigian, 2012, Human mutation.

Functional redundancy of exon 12 of BRCA2 revealed by a comprehensive analysis of the c.6853A>G (p.I2285V) variant

W. Foulkes, K. Offit, T. Kirchhoff, 2009, Human mutation.

Distinct patterns of germ‐line deletions in MLH1 and MSH2: the implication of Alu repetitive element in the genetic etiology of Lynch syndrome (HNPCC)

P. Hutter, W. Foulkes, P. gordon, 2006, Human mutation.

Novel targets in renal fibrosis based on bioinformatic analysis

Yuan Yuan, Lili Li, Xi Xiong, 2022, Frontiers in Genetics.

The Value of Multi-Modal Gene Screening in HNPCC in Quebec: Three Mutations in Mismatch Repair Genes that would have not been Correctly Identified by Genomic DNA Sequencing Alone

W. Foulkes, I. Thiffault, P. gordon, 2005, Familial Cancer.

Exome profiling of primary, metastatic and recurrent ovarian carcinomas in a BRCA1-positive patient

Emilie Lalonde, Jian Zhang, Jacek Majewski, 2013, BMC Cancer.