Yiming Wu

发表

Developing a one-step triplet-repeat primed PCR assay for diagnosing myotonic dystrophy.

Bai-Lin Wu, Y. An, Xiaoping Lan, 2018, Journal of genetics and genomics = Yi chuan xue bao.

Non-syndromic Oculocutaneous Albinism: Novel Genetic Variants and Clinical Follow Up of a Brazilian Pediatric Cohort

Y. Itan, R. Rosati, Aayushee Jain, 2020, Frontiers in Genetics.

LHCGR and ALMS1 defects likely cooperate in the development of polycystic ovary syndrome indicated by double-mutant mice.

Bai-Lin Wu, Rong Li, W. Tao, 2021, Journal of genetics and genomics = Yi chuan xue bao.

Genetic architecture, epigenetic influence and environment exposure in the pathogenesis of Autism

Bai-Lin Wu, Bai-Lin Wu, Yiming Wu, 2015, Science China Life Sciences.

Genome-wide prediction of pathogenic gain-and loss-of-function variants from ensemble learning of diverse feature set

P. Stenson, D. Cooper, A. Schlessinger, 2022 .

A feasibility study of noninvasive prenatal diagnosis in facioscapulohumeral muscular dystrophy type 1 in a Chinese family

Bo Wang, Yiming Wu, Hui Li, 2022, Frontiers in Genetics.

Genome-wide prediction of pathogenic gain- and loss-of-function variants from ensemble learning of a diverse feature set

P. Stenson, D. Cooper, A. Schlessinger, 2022, bioRxiv.

Identifying shared genetic factors underlying epilepsy and congenital heart disease in Europeans

P. Stenson, D. Cooper, C. S. Bayrak, 2022, Human Genetics.

Genetic architecture, epigenetic influence and environment exposure in the pathogenesis of Autism

Bai-Lin Wu, Yiming Wu, Li Yu, 2015, Science China Life Sciences.

Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population

Yiping Shen, Y. An, Hongyan Wang, 2015, BMC Medical Genomics.

Common and rare variant prediction and penetrance of IBD in a large, multi-ethnic, health system-based biobank cohort.

Judy H. Cho, M. Daly, J. Rioux, 2020, Gastroenterology.

A computational approach for detecting physiological homogeneity in the midst of genetic heterogeneity.

J. Casanova, L. Vallée, C. S. Bayrak, 2021, American journal of human genetics.

Human CRY1 variants associate with attention deficit/hyperactivity disorder.

J. Casanova, I. Kavakli, K. Bilguvar, 2020, The Journal of clinical investigation.

Haplotype-based non-invasive prenatal diagnosis of recessive dystrophic epidermolysis bullosa via targeted capture sequencing of maternal plasma.

Yiming Wu, Ming Li, J. Dou, 2023, The Journal of dermatology.

Genetic susceptibility to diabetic kidney disease is linked to promoter variants of XOR

Y. Itan, Liping Yu, G. Casalena, 2023, Nature Metabolism.

Recalling the pathology of Parkinson's disease; lacking exact figure of prevalence and genetic evidence in Asia with an alarming outcome: A time to step‐up

Muhammad Umair, A. Shah, Yiming Wu, 2021, Clinical genetics.

Analysis of CGG repeats in FMR1 in Chinese women with idiopathic premature ovarian failure.

Min Zhang, Bai-Lin Wu, Y. An, 2014, Reproductive biomedicine online.

Association study of CRP gene polymorphism and hypertension in Han Chinese population.

Chong Shen, Yiming Wu, Junming Tang, 2012, Gene.

Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients

Judy H. Cho, H. Ostrer, M. Daly, 2023, Nature communications.