Sylvie Tissier

发表

Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility.

S. Amselem, B. Crestani, B. Copin, 2016, American journal of human genetics.

Primary ciliary dyskinesia gene contribution in Tunisia: Identification of a major Mediterranean allele

S. Amselem, B. Copin, G. Montantin, 2020, Human mutation.

RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial Spokes.

S. Amselem, A. Clément, B. Copin, 2015, American journal of human genetics.

Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia.

S. Amselem, A. Loyens, A. Schmitt, 2019, American journal of human genetics.

TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus Flagella.

V. Drouin‐Garraud, A. Tassin, S. Amselem, 2020, American journal of human genetics.

Mutations in GAS8, a Gene Encoding a Nexin‐Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal Disorganization

S. Amselem, A. Clément, I. Sermet-Gaudelus, 2016, Human mutation.

Germline SFTPA1 mutation in familial idiopathic interstitial pneumonia and lung cancer.

S. Amselem, L. Gouya, A. Clément, 2016, Human molecular genetics.

Germline SFTPA 1 mutation in familial idiopathic interstitial pneumonia and lung cancer

S. Amselem, L. Gouya, A. Clément, 2016 .

Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients

Walaa F. Alsanie, S. Amselem, R. Lagha, 2022, Journal of Human Genetics.

Germline SFTPA1 mutation in familial idiopathic interstitial pneumonia and lung cancer.

S. Amselem, L. Gouya, A. Clément, 2016, Human molecular genetics.

Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility.

S. Amselem, B. Crestani, B. Copin, 2016, American journal of human genetics.