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Mutant ZP1 in Familial Infertility

The New England journal of medicine, 2014-03, Vol.370 (13), p.1220-1226

2014

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A hemizygous loss‐of‐function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia

Clinical genetics, 2024-07, Vol.106 (1), p.27-36

2024

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Biallelic mutations in MOS cause female infertility characterized by human early embryonic arrest and fragmentation

EMBO molecular medicine, 2021-12, Vol.13 (12), p.e14887-n/a

2021

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Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility

Human mutation, 2021-01, Vol.42 (1), p.31-36

2021

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Clinical and neonatal outcomes of patients of different ages following transfer of thawed cleavage embryos and blastocysts cultured from thawed cleavage-stage embryos

PloS one, 2018-11, Vol.13 (11), p.e0207340-e0207340

2018

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Histological endometrial dating: a reliable tool for personalized frozen-thawed embryo transfer in patients with repeated implantation failure in natural cycles

BMC pregnancy and childbirth, 2023-03, Vol.23 (1), p.199-199, Article 199

2023

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A newly discovered mutation in PICK1 in a human with globozoospermia

Asian journal of andrology, 2010-07, Vol.12 (4), p.556-560

2010

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The clinical and neonatal outcomes after stimulation of immotile spermatozoa using SperMagic medium

Andrologia, 2018-09, Vol.50 (7), p.e13056-n/a

2018

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Trophectoderm Biopsy Differentially Influences the Level of Serum β-Human Chorionic Gonadotropin With Different Embryonic Trophectoderm Scores in Early Pregnancy From 7847 Single-Blastocyst Transfer Cycles

Frontiers in endocrinology (Lausanne), 2022-02, Vol.13, p.794720-794720

2022

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Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency

Molecular genetics & genomic medicine, 2020-04, Vol.8 (4), p.e1165-n/a

2020

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Next‐generation sequence‐based preimplantation genetic testing for monogenic disease resulting from maternal mosaicism

Molecular genetics & genomic medicine, 2021-05, Vol.9 (5), p.e1662-n/a

2021

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Abnormalities in centrosome number in human embryos and embryonic stem cells

Molecular reproduction and development, 2016-05, Vol.83 (5), p.392-404

2016

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Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192

HGG advances, 2024-01, Vol.5 (1), p.100256-100256, Article 100256

2024

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Telomerase insufficiency induced telomere erosion accumulation in successive generations in dyskeratosis congenita family

Molecular genetics & genomic medicine, 2019-07, Vol.7 (7), p.e00709-n/a

2019

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Endometrial CD138 count appears to be a negative prognostic indicator for patients who have experienced previous embryo transfer failure

Fertility and sterility, 2019-12, Vol.112 (6), p.1103-1111

2019

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Tumor progression of culture-adapted human embryonic stem cells during long-term culture

Genes chromosomes & cancer, 2008-08, Vol.47 (8), p.665-679

2008

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Biallelic variants in IQCN cause sperm flagellar assembly defects and male infertility

Human reproduction (Oxford), 2023-07, Vol.38 (7), p.1390-1398

2023

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Stem cell characteristics and islet differentiation potential of human amniotic epithelial cells

Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2011-09, Vol.31 (9), p.1484

2011

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Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency

BMC medical genetics, 2018-01, Vol.19 (1), p.15-15, Article 15

2018

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A case report of a normal fertile woman with 46,XX/46,XY somatic chimerism reveals a critical role for germ cells in sex determination

Human reproduction (Oxford), 2024-04, Vol.39 (4), p.849-855

2024

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Over-expression of miR375 reduces glucose-induced insulin secretion in Nit-1 cells

Molecular biology reports, 2011-06, Vol.38 (5), p.3061-3065

2011

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Immune profiling and RNA-seq uncover the cause of partial unexplained recurrent implantation failure

International immunopharmacology, 2023-08, Vol.121, p.110513-110513, Article 110513

2023

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Isolation of human amniotic mesenchymal cells and their differentiation potential into islet-like cells in vitro

Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2011-01, Vol.31 (1), p.5

2011

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Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia

Journal of medical genetics, 2023-02, Vol.60 (2), p.144

2023

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Association of CTLA4 gene +49G/A polymorphism with HBV infection and HBV-related hepatocellular carcinoma in Hunan Han population

Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2010-08, Vol.30 (8), p.1838

2010

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Mutant ZP1 in Familial Infertility

A hemizygous loss‐of‐function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia

Biallelic mutations in MOS cause female infertility characterized by human early embryonic arrest and fragmentation

Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility

Clinical and neonatal outcomes of patients of different ages following transfer of thawed cleavage embryos and blastocysts cultured from thawed cleavage-stage embryos

Histological endometrial dating: a reliable tool for personalized frozen-thawed embryo transfer in patients with repeated implantation failure in natural cycles

A newly discovered mutation in PICK1 in a human with globozoospermia

The clinical and neonatal outcomes after stimulation of immotile spermatozoa using SperMagic medium

Trophectoderm Biopsy Differentially Influences the Level of Serum β-Human Chorionic Gonadotropin With Different Embryonic Trophectoderm Scores in Early Pregnancy From 7847 Single-Blastocyst Transfer Cycles

Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency

Next‐generation sequence‐based preimplantation genetic testing for monogenic disease resulting from maternal mosaicism

Abnormalities in centrosome number in human embryos and embryonic stem cells

Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192

Telomerase insufficiency induced telomere erosion accumulation in successive generations in dyskeratosis congenita family

Endometrial CD138 count appears to be a negative prognostic indicator for patients who have experienced previous embryo transfer failure

Tumor progression of culture-adapted human embryonic stem cells during long-term culture

Biallelic variants in IQCN cause sperm flagellar assembly defects and male infertility

Stem cell characteristics and islet differentiation potential of human amniotic epithelial cells

Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency

A case report of a normal fertile woman with 46,XX/46,XY somatic chimerism reveals a critical role for germ cells in sex determination

Over-expression of miR375 reduces glucose-induced insulin secretion in Nit-1 cells

Immune profiling and RNA-seq uncover the cause of partial unexplained recurrent implantation failure

Isolation of human amniotic mesenchymal cells and their differentiation potential into islet-like cells in vitro

Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia

Association of CTLA4 gene +49G/A polymorphism with HBV infection and HBV-related hepatocellular carcinoma in Hunan Han population

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