Claude Férec

On the sequence‐directed nature of human gene mutation: The role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease

David N Cooper, Hildegard Kehrer-Sawatzki, D. Cooper, 2011, Human mutation.

Sensitivity of the denaturing gradient gel electrophoresis technique in detection of known mutations and novel Asian mutations in the CFTR gene

Milan Macek, Ada Hamosh, Bernard Mercier, 1997, Human mutation.

Meta‐Analysis of gross insertions causing human genetic disease: Novel mutational mechanisms and the role of replication slippage

Peter D Stenson, David N Cooper, Nadia Chuzhanova, 2005, Human mutation.

Gene conversion causing human inherited disease: Evidence for involvement of non‐B‐DNA‐forming sequences and recombination‐promoting motifs in DNA breakage and repair

Nadia Chuzhanova, D. Cooper, R. Wells, 2009, Human mutation.

Signal peptide variants that impair secretion of pancreatic secretory trypsin inhibitor (SPINK1) cause autosomal dominant hereditary pancreatitis

Cinzia Battaggia, C. Férec, T. Wartmann, 2007, Human mutation.

The potential of oligonucleotides for therapeutic applications.

C. Férec, Y. Fichou, Yann Fichou, 2006, Trends in biotechnology.

Analysis of long-range interactions in primary human cells identifies cooperative CFTR regulatory elements

Josée Dostie, J. Dostie, C. Férec, 2015, Nucleic acids research.

Genomic rearrangements in inherited disease and cancer.

George P Patrinos, David N Cooper, Hildegard Kehrer-Sawatzki, 2010, Seminars in cancer biology.

Common CFTR haplotypes and susceptibility to chronic pancreatitis and congenital bilateral absence of the vas deferens

Olfert Landt, Milan Macek, Bernhard Steiner, 2011, Human mutation.