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/vufind/Search/Results?lookfor=%22Yinjie+Gao%22&type=Person&sort=year
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PubPharm (15)
1
The underlying cause of the simple virilizing phenotype in patients with 21-hydroxylase deficiency harboring P31L variant
in:
Frontiers in Endocrinology
| 2023
von
Zhiyuan Zhao
|
Yinjie Gao
|
Lin Lu
| +10
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2
181 Associations between multimodal immune biomarkers and clinical outcomes in a real-world non-small cell lung cancer cohort
in:
Journal for ImmunoTherapy of Cancer
| 2023
von
Justin Guinney
|
Rotem Ben-Shachar
|
Michelle M Stein
| +5
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3
Development and internal validation of a novel predictive model for SDHB mutations in pheochromocytomas and retroperitoneal paragangliomas
in:
Frontiers in Endocrinology
| 2023
von
Yue Zhou
|
Yinjie Gao
|
Xiaosen Ma
| +6
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4
Desmopressin Suppresses Gonadotropin-Induced Spermatogenesis in Patients With Pituitary Stalk Interruption Syndrome : A Retrospective, Single-Center Cohort Study
enthalten in:
Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
| 2021
von
Wen, J.
|
Jiangfeng, M.
|
Min, N.
| +7
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5
Recurrent Germline Mutations of CHEK2 as a New Susceptibility Gene in Patients with Pheochromocytomas and Paragangliomas
in:
International Journal of Endocrinology
| 2021
von
Yinjie Gao
|
Chao Ling
|
Xiaosen Ma
| +4
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6
The Bioinformatics Analysis of Aldosterone-Producing Adenoma and Verification of Differentially Expressed Genes
in:
International Journal of Endocrinology
| 2021
von
Yinjie Gao
|
Xiaosen Ma
|
Huiping Wang
| +4
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7
VariantStore: an index for large-scale genomic variant search
in:
Genome Biology
| 2021
von
Prashant Pandey
|
Yinjie Gao
|
Carl Kingsford
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8
Mutation of c.244G
in:
Orphanet Journal of Rare Diseases
| 2021
von
Bingqing Yu
|
Yinjie Gao
|
Jiangfeng Mao
| +3
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9
Local-Regional Recurrence of Pheochromocytoma/Paraganglioma: Characteristics, Risk Factors and Outcomes
in:
Frontiers in Endocrinology
| 2021
von
Yunying Cui
|
Xiaosen Ma
|
Yinjie Gao
| +4
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10
Clinical Characteristics and Spermatogenesis in Patients with Congenital Hypogonadotropic Hypogonadism Caused by FGFR1 Mutations
in:
International Journal of Endocrinology
| 2020
von
Shuying Li
|
Yaling Zhao
|
Min Nie
| +9
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