Jinong Feng

发表

Increased risk of idiopathic chronic pancreatitis in cystic fibrosis carriers

W. Greenhalf, J. Neoptolemos, S. Sommer, 2005, Human mutation.

SNPs in human miRNA genes affect biogenesis and function.

John J Rossi, Jin Yan, Guihua Sun, 2009, RNA.

Candidate gene analyses by scanning or brute force fluorescent sequencing: a comparison of DOVAM-S with gel-based and capillary-based sequencing.

S. Sommer, Jinong Feng, Jin Yan, 2007, Genetic testing.

Detection of mutations by single-strand conformation polymorphism (SSCP) analysis and SSCP-hybrid methods.

E. Hovig, W. H. Warren, A. Børresen, 2001, Current protocols in human genetics.

Three‐tiered noninvasive diagnosis in 96% of patients with Duchenne muscular dystrophy (DMD)

J. Mendell, S. Sommer, Jinong Feng, 2004, Human mutation.

Mutations in the dystrophin gene are associated with sporadic dilated cardiomyopathy.

J. Towbin, S. Sommer, Jinong Feng, 2002, Molecular genetics and metabolism.

MECP2 structural and 3′‐UTR variants in schizophrenia, autism and other psychiatric diseases: A possible association with autism

N. Craddock, E. Cook, I. Jones, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Comprehensive mutation scanning of the dystrophin gene in patients with nonsyndromic X-linked dilated cardiomyopathy.

J. Towbin, S. Sommer, Jinong Feng, 2002, Journal of the American College of Cardiology.

Identification of novel variants of the flavin-containing monooxygenase gene family in African Americans.

S. Sommer, Jinong Feng, D. Schlenk, 2003, Drug metabolism and disposition: the biological fate of chemicals.

Toward a Fluorescent SSCP Technique that Detects all Mutations: F-DOVAM-S

C. Mroske, Jinong Feng, Jin Yan, 2009 .

Scanning of estrogen receptor a and thyroid hormone receptor a genes in patients with psychiatric diseases

L. Peltonen, N. Craddock, D. Goldman, 2001 .

Mutations in the factor IX gene (F9) during the past 150 years have relative rates similar to ancient mutations

S. Sommer, Jinong Feng, W. Scaringe, 2002, Human mutation.

Mutation rates in the dystrophin gene: A hotspot of mutation at a CpG dinucleotide

J. Mendell, J. D. den Dunnen, S. Sommer, 2005, Human mutation.

Evidence for X-Chromosomal Schizophrenia Associated with microRNA Alterations

Jin Yan, John Rossi, Guihua Sun, 2009, PloS one.

High frequency of neurexin 1β signal peptide structural variants in patients with autism

Charles E. Schwartz, Edwin H. Cook, Jin Yan, 2006, Neuroscience Letters.

Neurexin 1α structural variants associated with autism

C. Skinner, C. Schwartz, S. Sommer, 2008, Neuroscience Letters.

Epidemiology of Doublet/Multiplet Mutations in Lung Cancers: Evidence that a Subset Arises by Chronocoordinate Events

S. Sommer, Jinong Feng, Jinong Feng, 2008, PloS one.

Identification of high risk DISC1 protein structural variants in patients with bipolar spectrum disorder

D. Grozeva, N. Craddock, E. Green, 2010, Neuroscience Letters.

Identification of high risk DISC1 structural variants with a 2% attributable risk for schizophrenia.

L. Heston, S. Sommer, Jinong Feng, 2008, Biochemical and biophysical research communications.

Systematic screening for mutations in the glycine receptor α2 subunit gene (GLRA2) in patients with schizophrenia and other psychiatric diseases

L. Peltonen, N. Craddock, L. DeLisi, 2001, Psychiatric genetics.

Analysis of the neuroligin 4Y gene in patients with autism

E. Cook, C. Skinner, C. Schwartz, 2008, Psychiatric genetics.

Missense Mutations in the MEFV Gene Are Associated with Fibromyalgia Syndrome and Correlate with Elevated IL-1β Plasma Levels

S. Sommer, J. Shively, Jinong Feng, 2009, PloS one.

Analysis of Cancer Mutation Signatures in Blood by a Novel Ultra-Sensitive Assay: Monitoring of Therapy or Recurrence in Non-Metastatic Breast Cancer

S. Sommer, Jinong Feng, L. Weiss, 2009, PloS one.

A mouse model for nonsense mutation bypass therapy shows a dramatic multiday response to geneticin

S. Sommer, P. Margaritis, K. High, 2007, Proceedings of the National Academy of Sciences.

Elevated frequency of ATM gene missense mutations in breast cancer relative to ethnically matched controls.

W. Bennett, M. Jung, A. Dritschilo, 2002, Cancer genetics and cytogenetics.

MECP2 coding sequence and 3′UTR variation in 172 unrelated autistic patients

Jin Yan, Catarina Correia, Astrid M Vicente, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Assessment of multiple displacement amplification in molecular epidemiology.

S. Sommer, Jinong Feng, Jin Yan, 2004, BioTechniques.

Variants in the α2A AR adrenergic receptor gene in psychiatric patients

E. Cook, D. Goldman, L. Heston, 1998 .

Vitamin D receptor variants in 192 patients with schizophrenia and other psychiatric diseases

N. Craddock, E. Cook, I. Jones, 2005, Neuroscience Letters.

ATM missense mutations are frequent in patients with breast cancer.

M. Jung, A. Dritschilo, S. Sommer, 2003, Cancer genetics and cytogenetics.

Absence of somatic ATM missense mutations in 58 mammary carcinomas.

A. Dritschilo, S. Sommer, Zefei Jiang, 2003, Cancer genetics and cytogenetics.

Highly sensitive mutation screening by REF with low concentrations of urea: A blinded analysis of a 2‐kb region of the p53 gene reveals two common haplotypes

S. Sommer, Shi Tang, Jinong Feng, 1999, Human mutation.

Toward a fluorescent single-strand conformation polymorphism technique that detects all mutations: F-DOVAM-S.

C. Mroske, Jinong Feng, Jin Yan, 2007, Analytical biochemistry.

Structural variants in the retinoid receptor genes in patients with schizophrenia and other psychiatric diseases

N. Craddock, E. Cook, I. Jones, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD‐PCR)

S. Sommer, P. Maciel, Jinong Feng, 2005, Human mutation.

Discovery of Potential New Gene Variants and Inflammatory Cytokine Associations with Fibromyalgia Syndrome by Whole Exome Sequencing

Xutao Deng, Xiwei Wu, K. Dery, 2013, PloS one.

SNPs in inflammatory genes CCL11, CCL4 and MEFV in a fibromyalgia family study

S. Neuhausen, Xiwei Wu, J. Shively, 2018, PloS one.

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients

N. Craddock, G. Oliveira, E. Cook, 2005, Molecular Psychiatry.

An in-frame deletion in the α2C adrenergic receptor is common in African–Americans

L. Peltonen, N. Craddock, L. DeLisi, 2001, Molecular Psychiatry.

Mutation scanning of the androgen receptor gene in patients with psychiatric disorders reveals highly conserved variants in alcoholic and phobia patients

N. Craddock, E. Cook, I. Jones, 2004, Psychiatric genetics.

EGFR somatic doublets in lung cancer are frequent and generally arise from a pair of driver mutations uncommonly seen as singlet mutations: one-third of doublets occur at five pairs of amino acids

S S Sommer, S. Sommer, Jinong Feng, 2008, Oncogene.

Detection of virtually all mutations-SSCP (DOVAM-S): a rapid method for mutation scanning with virtually 100% sensitivity.

Jinong Feng, J. Feng, S. Sommer, 1999, BioTechniques.

Risk factors for inhibitor formation in haemophilia: a prevalent case–control study

M. Trucco, Jinong Feng, Jin Yan, 2009, Haemophilia : the official journal of the World Federation of Hemophilia.