Guangxiu Lu

Central South University

H指数:39

被引数:5,278

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Genetic Rare Disease Prevention and Control: Family-Based Screening and Reproductive Interventions in Changsha

遗传罕见病预防与控制：基于家庭的筛查与生殖干预在长沙

Human Genetics and Genomics Advances

IF3.6

2025-08-180

OAAI

Pathogenic mutations in DMRTB1 cause human male infertility with non-obstructive azoospermia by impairing transcription regulation in spermatogenesis

DMRTB1基因的致病性突变通过损害精子发生过程中的转录调控，导致人类男性非梗阻性无精子症所致不育。

HUMAN REPRODUCTION

IF6.1

2025-06-010

OAAI

Maternal transcription factor OTX2 directly induces SETD1A and promotes embryonic genome activation in human pre-implantation embryos

母系转录因子OTX2直接诱导SETD1A并促进人早期胚胎中的胚胎基因组激活

SCIENCE CHINA-LIFE SCIENCES

IF9.5

2025-04-220

PRE

PRESENCE OF EMBRYO ALTERS MURINE DECIDUAL IMMUNE LANDSCAPE: INSIGHTS FROM THE BEAD-INDUCED DECIDUOMA MODEL

胚胎的存在改变了小鼠蜕膜免疫景观：来自珠诱导蜕膜瘤模型的见解

JOURNAL OF REPRODUCTIVE IMMUNOLOGY

IF2.9

2025-02-010

PRE

Preimplantation genetic testing for facioscapulohumeral dystrophy caused by contractions of 4q35 D4Z4 repeats

着床前遗传学检测用于检测由4q35 D4Z4重复序列缩短引起的面部肩胛肱型肌营养不良症

Reproductive BioMedicine Online

IF3.5

2025-02-010

PRE

Genetic Analysis and Reproductive Interventions for Two Rare Families Affected by Severe Haemophilia A

HAEMOPHILIA

IF3

2024-12-040

PRE

Women with FSHR-inactivating mutations causing resistant ovarian syndrome benefit from oocyte in-vitro maturation

携带导致抵抗性卵巢综合征的FSHR失活突变的女性，可从卵母细胞体外成熟中获益。

REPRODUCTIVE BIOMEDICINE ONLINE

IF3.5

2024-11-010

PRE

Homozygous ACTL9 mutations cause irregular mitochondrial sheath arrangement and abnormal flagellum assembly in spermatozoa and male infertility

JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

IF2.7

2024-07-040

PRE

Human umbilical cord-derived mesenchymal stem cell transplantation improves the long COVID

JOURNAL OF MEDICAL VIROLOGY

IF4.6

2024-06-200

PRE

A single-cell transcriptome atlas of human euploid and aneuploid blastocysts

NATURE GENETICS

IF31.8

2024-06-051

PRE

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

一例46，XX/46，XY体细胞嵌合体的正常可育妇女的病例报告揭示了生殖细胞在性别决定中的关键作用

HUMAN REPRODUCTION

IF6.1

2024-02-281

PRE

Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia

MOLECULAR HUMAN REPRODUCTION

IF3.5

2024-01-222

PRE

Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice

DNAH3中的双等位基因变体导致人类和小鼠的男性不育和弱畸形性精子症

HUMAN REPRODUCTION OPEN

IF11.1

2024-01-115

OAAI

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

HUMAN GENETICS AND GENOMICS ADVANCES

IF3.6

2024-01-013

OAAI

Transcriptomic profiles reveal the characteristics of oocytes and cumulus cells at GV, MI, and MII in follicles before ovulation

转录组图谱揭示了排卵前卵泡中GV，MI和MII处卵母细胞和卵丘细胞的特征

JOURNAL OF OVARIAN RESEARCH

IF4.2

2023-11-228

OAAI

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

ASIAN JOURNAL OF ANDROLOGY

IF2.7

2023-11-172

OAAI

Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression

CELL DISCOVERY

IF12.5

2023-08-221

OAAI

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

免疫分析和rna-seq揭示了部分原因不明的复发性植入失败的原因

INTERNATIONAL IMMUNOPHARMACOLOGY

IF4.7

2023-08-012

PRE

Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia

HUMAN REPRODUCTION

IF6.1

2023-05-169

PRE

Single-cell transcriptome analysis of NEUROG3+cells during pancreatic endocrine differentiation with small molecules

STEM CELL RESEARCH & THERAPY

IF7.3

2023-04-250

OAAI

Guangxiu Lu

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