You-ying Mao

发表

Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT.

S. Mane, S. Bauer, V. Tasic, 2021, Genetics in medicine : official journal of the American College of Medical Genetics.

DAAM2 Variants Cause Nephrotic Syndrome via Actin Dysregulation.

Thomas M. Kitzler, S. Mane, R. Lifton, 2020, American journal of human genetics.

Immunometabolism in the pathogenesis of systemic lupus erythematosus

You-ying Mao, Chenxing Zhang, Huiyu Wang, 2020, Journal of translational autoimmunity.

Addition of cyclosporine/tacrolimus for pediatric relapsed lupus nephritis during mycophenolate mofetil maintenance therapy

Tong-Xin Chen, Wei Zhou, You-ying Mao, 2018, The Journal of international medical research.

Clinical manifestations, immunological features and prognosis of Chinese pediatric systemic lupus erythematosus: A single‐center study

Tong-Xin Chen, W. Zhou, You-ying Mao, 2019, International journal of rheumatic diseases.

Henoch–Schönlein purpura in 535 Chinese children: clinical features and risk factors for renal involvement

Tong-Xin Chen, W. Zhou, You-ying Mao, 2014, The Journal of international medical research.

Generation of Monogenic Candidate Genes for Human Nephrotic Syndrome Using 3 Independent Approaches

Thomas M. Kitzler, S. Mane, H. Rehm, 2020, Kidney international reports.

Microscopic Polyangitis in Pediatric Systemic Lupus Erythematosus: A Unique Presentation of Pulmonary - Renal Syndrome and Case Report of an Overlap Syndrome

Wei Zhou, You-ying Mao, Chenxing Zhang, 2020 .

Incidence and clinical features of paediatric vasculitis in Eastern China: 14-year retrospective study, 1999–2013

Tong-Xin Chen, Wei Zhou, You-ying Mao, 2016, The Journal of international medical research.

De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis.

Thomas M. Kitzler, V. Jobanputra, D. Goldstein, 2021, American journal of human genetics.

A retrospective study of nine patients with progressive pseudorheumatoid dysplasia: to explore early diagnosis and further treatment

Jian Wang, You-ying Mao, Yongguo Yu, 2021, Clinical Rheumatology.

Systematical analysis of nine Chinese patients with progressive pseudorheumatoid dysplasia and assessment of calcitriol treatment

Wei Zhou, Jian Wang, You-ying Mao, 2020 .

Recessive Mutations in SYNPO2 as a Candidate of Monogenic Nephrotic Syndrome

Thomas M. Kitzler, S. Mane, R. Lifton, 2020, Kidney international reports.

Vincristine alleviates adriamycin-induced nephropathy through stabilizing actin cytoskeleton

W. Zhou, You-ying Mao, Zhen Zhang, 2017, Cell & Bioscience.

Recessive NOS1AP variants impair actin remodeling and cause glomerulopathy in humans and mice

S. Mane, S. Howden, R. Lifton, 2021, Science Advances.

Donor-derived hypouricemia in irrelevant recipients caused by kidney transplantation

Jianghua Chen, Hong Jiang, Jianyong Wu, 2020, Annals of translational medicine.

Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome.

M. Skalej, S. Mane, R. Lifton, 2021, Journal of the American Society of Nephrology : JASN.

Treatment and outcome of IgA nephropathy in children from one single center experience

Wei Zhou, You-ying Mao, Chenxing Zhang, 2023, BMC Pediatrics.

Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models

Thomas M. Kitzler, S. Mane, R. Lifton, 2022, American journal of medical genetics. Part A.

Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.

Kristen M. Laricchia, Thomas M. Kitzler, D. MacArthur, 2020, American journal of human genetics.