Zhi-yong Ji

Xiamen, China

Last Updated: 09/26/2026

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Found 13 publications

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

Sperm-egg fusion disorder in a Chinese male patient was associated with a rare ADAM20 variant.

Sperm-egg fusion disorder in a Chinese male patient was associated with a rare ADAM20 variant.

Journal: Oncotarget

Published: May 24, 2017

Globozoospermic infertility associated with balanced DPY19L2 translocation/gene deletion at the chromosomal breakpoint.

Globozoospermic infertility associated with balanced DPY19L2 translocation/gene deletion at the chromosomal breakpoint.

Journal: Asian journal of andrology

Published: March 09, 2017

Diagnosis of a Chinese man with 45,X/46,X,i(Y)(q10)/47,X,i(Y) (q10) ×2 mosaic Turner syndrome.

Diagnosis of a Chinese man with 45,X/46,X,i(Y)(q10)/47,X,i(Y) (q10) ×2 mosaic Turner syndrome.

Journal: Asian journal of andrology

Published: January 17, 2017

A successful pregnancy by intracytoplasmic sperm injection using ejaculate sperm from an infertile man with 46, XX/46, XY true hermaphrodite.

A successful pregnancy by intracytoplasmic sperm injection using ejaculate sperm from an infertile man with 46, XX/46, XY true hermaphrodite.

Journal: Asian journal of andrology

Published: December 02, 2016

Showing 1-12 of 13

Last Updated: 09/26/2026