Detalhe da pesquisa
1.
Novel frameshift mutation in STK33 is associated with asthenozoospermia and multiple morphological abnormalities of the flagella.
Hum Mol Genet
; 30(21): 1977-1984, 2021 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-34155512
2.
PedMiner: a tool for linkage analysis-based identification of disease-associated variants using family based whole-exome sequencing data.
Brief Bioinform
; 22(3)2021 05 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32393981
3.
A recessive ACTL7A founder variant leads to male infertility due to acrosome detachment in Pakistani Pashtuns.
Clin Genet
; 104(5): 564-570, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37286336
4.
Research on hand, foot and mouth disease incidence forecasting using hybrid model in mainland China.
BMC Public Health
; 23(1): 619, 2023 03 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-37003988
5.
The research on TBATS and ELM models for prediction of human brucellosis cases in mainland China: a time series study.
BMC Infect Dis
; 22(1): 934, 2022 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36510150
6.
Research of Combined ES-BP Model in Predicting Syphilis Incidence 1982-2020 in Mainland China.
Iran J Public Health
; 52(10): 2063-2072, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37899935
7.
A new hybrid model SARIMA-ETS-SVR for seasonal influenza incidence prediction in mainland China.
J Infect Dev Ctries
; 17(11): 1581-1590, 2023 11 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38064398
8.
Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and mice.
JCI Insight
; 8(3)2023 02 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36752199
9.
Loss-of-function variants in KCTD19 cause non-obstructive azoospermia in humans.
iScience
; 26(7): 107193, 2023 Jul 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37485353
10.
Prediction of global omicron pandemic using ARIMA, MLR, and Prophet models.
Sci Rep
; 12(1): 18138, 2022 10 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36307471
11.
The research of SARIMA model for prediction of hepatitis B in mainland China.
Medicine (Baltimore)
; 101(23): e29317, 2022 Jun 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35687775
12.
The research of ARIMA, GM(1,1), and LSTM models for prediction of TB cases in China.
PLoS One
; 17(2): e0262734, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35196309
13.
FertilityOnline: A Straightforward Pipeline for Functional Gene Annotation and Disease Mutation Discovery.
Genomics Proteomics Bioinformatics
; 20(3): 455-465, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34954426
14.
MeiosisOnline: A Manually Curated Database for Tracking and Predicting Genes Associated With Meiosis.
Front Cell Dev Biol
; 9: 673073, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34485275
15.
Novel Loss-of-Function Mutations in DNAH1 Displayed Different Phenotypic Spectrum in Humans and Mice.
Front Endocrinol (Lausanne)
; 12: 765639, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34867808
16.
Biallelic Variants in CFAP61 Cause Multiple Morphological Abnormalities of the Flagella and Male Infertility.
Front Cell Dev Biol
; 9: 803818, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35174165
17.
Novel biallelic loss-of-function mutations in CFAP43 cause multiple morphological abnormalities of the sperm flagellum in Pakistani families.
Asian J Androl
; 23(6): 627-632, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34100391
18.
Computationally predicted pathogenic USP9X mutation identified in infertile men does not affect spermatogenesis in mice.
Zool Res
; 43(2): 225-228, 2022 03 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-35084129