PubRank

Cuiping Hou

Author PubWeight™ 85.86‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature 2009 9.47
2 Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature 2009 7.39
3 Identification of ALK as a major familial neuroblastoma predisposition gene. Nature 2008 7.38
4 Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms. Nucleic Acids Res 2008 4.22
5 Variants of DENND1B associated with asthma in children. N Engl J Med 2009 4.18
6 Copy number variation at 1q21.1 associated with neuroblastoma. Nature 2009 4.10
7 Common variants at five new loci associated with early-onset inflammatory bowel disease. Nat Genet 2009 3.82
8 Chromosome 6p22 locus associated with clinically aggressive neuroblastoma. N Engl J Med 2008 3.80
9 No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics. Am J Psychiatry 2008 3.23
10 Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease. Am J Hum Genet 2009 3.19
11 From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes. PLoS Genet 2009 2.99
12 Common variations in BARD1 influence susceptibility to high-risk neuroblastoma. Nat Genet 2009 2.47
13 Integrative genomics identifies LMO1 as a neuroblastoma oncogene. Nature 2010 2.21
14 Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy. Genome Res 2009 2.02
15 Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample. Am J Hum Genet 2006 1.89
16 Strong synaptic transmission impact by copy number variations in schizophrenia. Proc Natl Acad Sci U S A 2010 1.85
17 Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects. Hum Mol Genet 2010 1.81
18 Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma. Nat Genet 2012 1.74
19 Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis. Am J Hum Genet 2013 1.63
20 Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. Nat Genet 2011 1.63
21 Genome-wide association identifies diverse causes of common variable immunodeficiency. J Allergy Clin Immunol 2011 1.60
22 A genome-wide study reveals copy number variants exclusive to childhood obesity cases. Am J Hum Genet 2010 1.36
23 Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene. Diabetes 2009 1.34
24 The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature. BMC Med Genet 2010 1.17
25 Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI. Diabetes 2009 1.10
26 Common variation at BARD1 results in the expression of an oncogenic isoform that influences neuroblastoma susceptibility and oncogenicity. Cancer Res 2012 1.09
27 GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. Hum Mol Genet 2012 1.09
28 Autosomal dominant hypoparathyroidism caused by germline mutation in GNA11: phenotypic and molecular characterization. J Clin Endocrinol Metab 2014 1.06
29 Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia. Am J Hum Genet 2004 1.03
30 A missense mutation in ANKRD26 segregates with thrombocytopenia. Blood 2013 0.93
31 DTNBP1 (Dystrobrevin binding protein 1) and schizophrenia: association evidence in the 3' end of the gene. Hum Hered 2007 0.93
32 Neuregulin 1 (NRG1 ) and schizophrenia: analysis of a US family sample and the evidence in the balance. Psychol Med 2005 0.89
33 The missense variation landscape of FTO, MC4R, and TMEM18 in obese children of African Ancestry. Obesity (Silver Spring) 2013 0.85
34 Cadmium accumulation and tolerance of two safflower cultivars in relation to photosynthesis and antioxidative enzymes. Bull Environ Contam Toxicol 2010 0.78
35 AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate. JIMD Rep 2014 0.76
36 Erratum to: AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate. JIMD Rep 2014 0.76
37 Molecular Barium Hydrido Complex Stabilized by a Super Bulky Hydrotris(pyrazolyl)borate Ligand. Angew Chem Int Ed Engl 2017 0.75