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Chun-Ming Pan

Shanghai Jiao Tong University

H指数:24

被引数:3,559

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Mimecan, a Hormone Abundantly Expressed in Adipose Tissue, Reduced Food Intake Independently of Leptin Signaling

IF10.8

2015-11-0122

OAAI

Characterization of Somatic Mutations in Air Pollution-Related Lung Cancer

IF10.8

2015-06-0174

OAAI

Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations

HUMAN MOLECULAR GENETICS

IF3.2

2014-05-2233

OAAI

Genomic landscape of CD34+ hematopoietic cells in myelodysplastic syndrome and gene mutation profiles as prognostic markers

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2014-05-2153

OAAI

Phenotypic and molecular characteristics in eleven Chinese patients with 5α-reductase Type 2 deficiency

CLINICAL ENDOCRINOLOGY

IF2.4

2014-04-2134

PREAI

Refined association of TSH receptor susceptibility locus to Graves' disease in the Chinese Han population

EUROPEAN JOURNAL OF ENDOCRINOLOGY

IF5.2

2014-01-0115

OAAI

Identification of BACH2 as a susceptibility gene for Graves' disease in the Chinese Han population based on a three-stage genome-wide association study

IF3.6

2013-12-1220

PREAI

Association between the interleukin-13 gene and development of chronic obstructive pulmonary disease in southern Chinese Han population: a case-control study

CHINESE MEDICAL JOURNAL

IF7.3

2013-12-058

OA

The association of SCGB3A2 polymorphisms with the risk of Graves' disease: a meta-analysis

IF2.9

2013-08-103

PREAI

Dense mapping of IL2RA shows no association with Graves' disease in Chinese Han population

CLINICAL ENDOCRINOLOGY

IF2.4

2013-04-278

PREAI

Robust evidence for five new Graves disease risk loci from a staged genome-wide association analysis

HUMAN MOLECULAR GENETICS

IF3.2

2013-04-2383

OAAI

Aldosterone directly affects apelin expression and secretion in adipocytes

醛固酮直接影响脂肪细胞apelin的表达和分泌

JOURNAL OF MOLECULAR ENDOCRINOLOGY

IF3.8

2013-04-0216

OAAI

A novel intronic mutation and a missense mutation of MEN1 identified in two Chinese families with multiple endocrine neoplasia type 1

在两个患有多发性内分泌肿瘤1型的中国家庭中鉴定出MEN1的新型内含子突变和错义突变

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION

IF3.5

2013-03-012

PREAI

Identification of a novel mutation in CYP17A1 gene

TRANSLATIONAL RESEARCH

IF5.9

2013-01-015

PREAI

The influence of the genetic and non-genetic factors on bone mineral density and osteoporotic fractures in Chinese women

IF2.9

2012-07-1415

PREAI

Single-nucleotide polymorphisms in the TSPYL-4 and NT5DC1 genes are associated with susceptibility to chronic obstructive pulmonary disease

MOLECULAR MEDICINE REPORTS

IF3.5

2012-06-2512

PREAI

Identification of a locus (DSP2) for disseminated superficial porokeratosis at chromosome 12q21.2-24.21

CLINICAL AND EXPERIMENTAL DERMATOLOGY

IF2.8

2012-06-117

OAAI

Functional study of an aberrant splicing variant of the human luteinizing hormone (LH) receptor

MOLECULAR HUMAN REPRODUCTION

IF3.5

2011-10-145

OAAI

A unique exonic splicing mutation in the CYP17A1 gene as the cause for steroid 17α-hydroxylase deficiency

EUROPEAN JOURNAL OF ENDOCRINOLOGY

IF5.2

2011-04-0122

OAAI

Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia

NATURE GENETICS

IF31.8

2011-03-13733

PREAI