Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals newDNAH1mutations

Familial Cases ◽

Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations

Clinical Genetics ◽

10.1111/cge.13604 ◽

2019 ◽

Vol 96 (5) ◽

pp. 394-401 ◽

Cited By ~ 6

Author(s):

Zine‐Eddine Kherraf ◽

Caroline Cazin ◽

Charles Coutton ◽

Amir Amiri‐Yekta ◽

Guillaume Martinez ◽

...

Keyword(s):

Exome Sequencing ◽

Whole Exome Sequencing ◽

Decision letter for "Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations"

10.1111/cge.13604/v2/decision1 ◽

2019 ◽

Keyword(s):

Exome Sequencing ◽

Whole Exome Sequencing ◽

Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity

Kidney International ◽

10.1038/ki.2015.317 ◽

2016 ◽

Vol 89 (2) ◽

pp. 468-475 ◽

Cited By ~ 41

Author(s):

Daniela A. Braun ◽

Markus Schueler ◽

Jan Halbritter ◽

Heon Yung Gee ◽

Jonathan D. Porath ◽

...

Keyword(s):

Exome Sequencing ◽

Whole Exome Sequencing ◽

Childhood Onset ◽

Familial Cases ◽

Review for "Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations"

10.1111/cge.13604/v1/review2 ◽

2019 ◽

Keyword(s):

Exome Sequencing ◽

Whole Exome Sequencing ◽

Decision letter for "Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations"

10.1111/cge.13604/v1/decision1 ◽

2019 ◽

Keyword(s):

Exome Sequencing ◽

Whole Exome Sequencing ◽

Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella

Human Reproduction ◽

10.1093/humrep/dey264 ◽

2018 ◽

Vol 33 (10) ◽

pp. 1973-1984 ◽

Cited By ~ 35

Author(s):

Guillaume Martinez ◽

Zine-Eddine Kherraf ◽

Raoudha Zouari ◽

Selima Fourati Ben Mustapha ◽

Antoine Saut ◽

...

Keyword(s):

Exome Sequencing ◽

Whole Exome Sequencing ◽

Review for "Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations"

10.1111/cge.13604/v2/review1 ◽

2019 ◽

Keyword(s):

Exome Sequencing ◽

Whole Exome Sequencing ◽

Review for "Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations"

10.1111/cge.13604/v1/review1 ◽

2019 ◽

Keyword(s):

Exome Sequencing ◽

Whole Exome Sequencing ◽

Author response for "Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations"

10.1111/cge.13604/v2/response1 ◽

2019 ◽

Author(s):

Zine‐Eddine Kherraf ◽

Caroline Cazin ◽

Charles Coutton ◽

Amir Amiri‐Yekta ◽

Guillaume Martinez ◽

...

Keyword(s):

Exome Sequencing ◽

Whole Exome Sequencing ◽

Author Response ◽

Whole Exome Sequencing (WES) in Familien mit linksventrikulärer Ausfluβtraktobstruktion (LVOTO)

The Thoracic and Cardiovascular Surgeon ◽

10.1055/s-0034-1393993 ◽

2014 ◽

Vol 62 (S 02) ◽

Author(s):

M. Hitz ◽

S. Al-Turki ◽

A. Schalinski ◽

U. Bauer ◽

T. Pickardt ◽

...

Keyword(s):

Exome Sequencing ◽

Whole Exome Sequencing ◽