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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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XRCC2 mutation causes premature ovarian insufficiency as well as non‐obstructive azoospermia in humans

Clinical genetics, 2019-03, Vol.95 (3), p.442-443

2019

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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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In-Frame Variants in STAG3 Gene Cause Premature Ovarian Insufficiency

Frontiers in genetics, 2019-11, Vol.10, p.1016-1016

2019

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Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans

Asian journal of andrology, 2022-07, Vol.24 (4), p.359-366

2022

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Defects in phospholipase C zeta cause polyspermy and low fertilization after conventional IVF: not just ICSI failure

Asian journal of andrology, 2024-03, Vol.26 (2), p.175-182

2024

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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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X‐chromosome inactivation pattern of amniocytes predicts the risk of dystrophinopathy in fetal carriers of DMD mutations

Prenatal diagnosis, 2019-07, Vol.39 (8), p.603-608

2019

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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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Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia

Frontiers in genetics, 2022-08, Vol.13, p.936264-936264

2022

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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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Inner cell mass incarceration in 8-shaped blastocysts does not increase monozygotic twinning in preimplantation genetic diagnosis and screening patients

PloS one, 2018-01, Vol.13 (1), p.e0190776-e0190776

2018

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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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miR-200a-3p promotes β-Amyloid-induced neuronal apoptosis through down-regulation of SIRT1 in Alzheimer’s disease

Journal of biosciences, 2017-09, Vol.42 (3), p.397-404

2017

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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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Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction

BMC medical genetics, 2018-10, Vol.19 (1), p.186-186, Article 186

2018

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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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Mutant ZP1 in Familial Infertility

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

XRCC2 mutation causes premature ovarian insufficiency as well as non‐obstructive azoospermia in humans

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

In-Frame Variants in STAG3 Gene Cause Premature Ovarian Insufficiency

Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans

Defects in phospholipase C zeta cause polyspermy and low fertilization after conventional IVF: not just ICSI failure

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

X‐chromosome inactivation pattern of amniocytes predicts the risk of dystrophinopathy in fetal carriers of DMD mutations

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

Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia

A newly discovered mutation in PICK1 in a human with globozoospermia

Inner cell mass incarceration in 8-shaped blastocysts does not increase monozygotic twinning in preimplantation genetic diagnosis and screening patients

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

miR-200a-3p promotes β-Amyloid-induced neuronal apoptosis through down-regulation of SIRT1 in Alzheimer’s disease

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

Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction

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

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