Lu Ding
Xiamen, China
Last Updated: 09/26/2026
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Found 21 publications
DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagella.
Journal: Annals of human genetics
Published: May 06, 2019
Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotype.
Journal: Journal of human genetics
Published: April 09, 2019
EIF4G1 is a novel candidate gene associated with severe asthenozoospermia.
Journal: Molecular genetics & genomic medicine
Published: January 16, 2019
Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF).
Journal: Journal of medical genetics
Published: December 18, 2018
DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagella.
Journal: Clinical genetics
Published: December 02, 2018
Biallelic mutations in PMFBP1 cause acephalic spermatozoa.
Journal: Clinical genetics
Published: July 24, 2018
Two cases of complex balanced autosomal translocations associated with severe oligozoospermia.
Journal: Gene
Published: January 29, 2018
Familial fragile X syndrome: A pedigree analysis
Journal: Zhonghua nan ke xue = National journal of andrology
Published: October 27, 2017
TSGA10 is a novel candidate gene associated with acephalic spermatozoa.
Journal: Clinical genetics
Published: July 31, 2017
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.
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.
Journal: Asian journal of andrology
Published: December 02, 2016
Last Updated: 09/26/2026