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J

Jinghua Yin

zhejiang international studies university

H指数:16

被引数:813

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Smart governance for sustainable development: Stage-specific effects and regional heterogeneity in a global empirical framework

可持续发展背景下的智慧治理：全球实证框架中的阶段性效应与区域异质性

Structural Change and Economic Dynamics

IF5.5

2025-12-270

PRE

Association between in vitro fertilization-embryo transfer and hearing loss: risk factors for hearing loss among twin infants in a cohort study

EUROPEAN JOURNAL OF PEDIATRICS

IF2.6

2023-01-130

OA

The individual and joint associations of depression and sleep duration with cardiometabolic diseases and mortality: A prospective cohort study

抑郁症和睡眠时间与心脏代谢疾病和死亡率的个体和联合关联: 一项前瞻性队列研究

ATHEROSCLEROSIS

IF5.7

2022-11-0110

OAAI

Association between healthy lifestyle and the occurrence of cardiometabolic multimorbidity in hypertensive patients: a prospective cohort study of UK Biobank

健康生活方式与高血压患者心脏代谢多发病的关系: 英国生物银行的前瞻性队列研究

CARDIOVASCULAR DIABETOLOGY

IF10.6

2022-10-0133

OAAI

Shift Work and the Risk of Cardiometabolic Multimorbidity Among Patients With Hypertension: A Prospective Cohort Study of UK Biobank

JOURNAL OF THE AMERICAN HEART ASSOCIATION

IF5.3

2022-09-0626

OAAI

Association of mood disorder with cardiometabolic multimorbidity trajectory and life expectancy, a prospective cohort study

心境障碍与心脏代谢多发病轨迹和预期寿命的关联，一项前瞻性队列研究

JOURNAL OF AFFECTIVE DISORDERS

IF4.9

2022-09-016

PRE

Association of healthy sleep pattern with the risk of cardiovascular disease and all-cause mortality among people with diabetes: A prospective cohort study

DIABETES RESEARCH AND CLINICAL PRACTICE

IF7.4

2022-04-0121

PRE

E4BP4-mediated inhibition of T follicular helper cell differentiation is compromised in autoimmune diseases

JOURNAL OF CLINICAL INVESTIGATION

IF13.6

2020-06-0242

OA

Effectiveness and Safety of Different Once-Daily Doses of Adrenocorticotropic Hormone for Infantile Spasms

PEDIATRIC DRUGS

IF3.3

2017-04-1817

PREAI

Organ-specific biomarkers in lupus

AUTOIMMUNITY REVIEWS

IF8.3

2017-04-0151

PREAI

Compound heterozygous PLEC mutations in a patient of consanguineous parentage with epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia

INTERNATIONAL JOURNAL OF DERMATOLOGY

IF3.2

2014-09-1010

PREAI

Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome

HUMAN MOLECULAR GENETICS

IF3.2

2014-08-2845

OAAI

New and Recurrent SERPINB7 Mutations in Seven Chinese Patients with Nagashima-Type Palmoplantar Keratosis

JOURNAL OF INVESTIGATIVE DERMATOLOGY

IF5.7

2014-08-0141

OAAI

Mutation in AQP5, Encoding Aquaporin 5, Causes Palmoplantar Keratoderma Bothnia Type

JOURNAL OF INVESTIGATIVE DERMATOLOGY

IF5.7

2014-01-0136

OAAI

A new germline mutation in KIT associated with diffuse cutaneous mastocytosis in a Chinese family

CLINICAL AND EXPERIMENTAL DERMATOLOGY

IF2.8

2013-12-0221

PREAI

A novel nonsense mutation in the CDSN gene underlying hypotrichosis simplex of the scalp in a Chinese family

CLINICAL AND EXPERIMENTAL DERMATOLOGY

IF2.8

2013-06-087

PREAI

New mutations in the PLEC gene in a Chinese patient with epidermolysis bullosa simplex with muscular dystrophy

CLINICAL AND EXPERIMENTAL DERMATOLOGY

IF2.8

2013-03-184

PREAI

Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2012-11-0158

OAAI