Yan-wei Sha

No. 10 Zhenhai Road
Xiamen, 361003, China

Last Updated: 09/26/2026

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Found 27 publications

Biallelic mutations in spermatogenesis and centriole-associated 1 like (SPATC1L) cause acephalic spermatozoa syndrome and male infertility.

Biallelic mutations in spermatogenesis and centriole-associated 1 like (SPATC1L) cause acephalic spermatozoa syndrome and male infertility.

Journal: Asian journal of andrology

Published: July 02, 2021

Novel IFT140 variants cause spermatogenic dysfunction in humans.

Novel IFT140 variants cause spermatogenic dysfunction in humans.

Journal: Molecular genetics & genomic medicine

Published: February 02, 2019

Biallelic mutations in PMFBP1 cause acephalic spermatozoa.

Biallelic mutations in PMFBP1 cause acephalic spermatozoa.

Journal: Clinical genetics

Published: July 24, 2018

Patients with multiple morphological abnormalities of the sperm flagella harbouring CFAP44 or CFAP43 mutations have a good pregnancy outcome following intracytoplasmic sperm injection.

Patients with multiple morphological abnormalities of the sperm flagella harbouring CFAP44 or CFAP43 mutations have a good pregnancy outcome following intracytoplasmic sperm injection.

Journal: Andrologia

Published: June 24, 2018

Identification of a novel mutation in FGFR1 gene in patients with Kallmann syndrome by high throughput sequencing.

Identification of a novel mutation in FGFR1 gene in patients with Kallmann syndrome by high throughput sequencing.

Journal: Systems biology in reproductive medicine

Published: April 17, 2018

Two cases of complex balanced autosomal translocations associated with severe oligozoospermia.

Two cases of complex balanced autosomal translocations associated with severe oligozoospermia.

Journal: Gene

Published: January 29, 2018

Novel Mutations in CFAP44 and CFAP43 Cause Multiple Morphological Abnormalities of the Sperm Flagella (MMAF).

Novel Mutations in CFAP44 and CFAP43 Cause Multiple Morphological Abnormalities of the Sperm Flagella (MMAF).

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: December 27, 2017

TDRD6 is associated with oligoasthenoteratozoospermia by sequencing the patient from a consanguineous family.

TDRD6 is associated with oligoasthenoteratozoospermia by sequencing the patient from a consanguineous family.

Journal: Gene

Published: December 04, 2017

Familial fragile X syndrome: A pedigree analysis

Familial fragile X syndrome: A pedigree analysis

Journal: Zhonghua nan ke xue = National journal of andrology

Published: October 27, 2017

Genetic contribution of SUN5 mutations to acephalic spermatozoa in Fujian China.

Genetic contribution of SUN5 mutations to acephalic spermatozoa in Fujian China.

Journal: Gene

Published: September 27, 2017

A novel mutation in HAUS7 results in severe oligozoospermia in two brothers.

A novel mutation in HAUS7 results in severe oligozoospermia in two brothers.

Journal: Gene

Published: June 29, 2017

Use of targeted sequence capture and high-throughput sequencing identifies a novel PKD1 mutation involved in adult polycystic kidney disease.

Use of targeted sequence capture and high-throughput sequencing identifies a novel PKD1 mutation involved in adult polycystic kidney disease.

Journal: Gene

Published: June 25, 2017

Showing 1-12 of 27

Last Updated: 09/26/2026