| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Absence of association between SERPINE2 genetic polymorphisms and chronic obstructive pulmonary disease in Han Chinese: a case-control cohort study
|
Zhong, Li
|
|
2009
|
10 |
1 |
|
artikel
|
| 2 |
ACE (I/D) polymorphism and response to treatment in coronary artery disease: a comprehensive database and meta-analysis involving study quality evaluation
|
Kitsios, Georgios
|
|
2009
|
10 |
1 |
|
artikel
|
| 3 |
Additive effect of LRP8/APOER2 R952Q variant to APOE ε2/ε3/ε4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study
|
Martinelli, Nicola
|
|
2009
|
10 |
1 |
|
artikel
|
| 4 |
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review
|
Fernández, Luis
|
|
2009
|
10 |
1 |
|
artikel
|
| 5 |
A functional polymorphism in the SPINK5 gene is associated with asthma in a Chinese Han Population
|
Liu, Qiji
|
|
2009
|
10 |
1 |
|
artikel
|
| 6 |
ALDH1A2 (RALDH2) genetic variation in human congenital heart disease
|
Pavan, Marilene
|
|
2009
|
10 |
1 |
|
artikel
|
| 7 |
A MANBA mutation resulting in residual beta-mannosidase activity associated with severe leukoencephalopathy: a possible pseudodeficiency variant
|
Sabourdy, Frédérique
|
|
2009
|
10 |
1 |
|
artikel
|
| 8 |
A mitotic recombination map proximal to the APC locus on chromosome 5q and assessment of influences on colorectal cancer risk
|
Howarth, Kimberley
|
|
2009
|
10 |
1 |
|
artikel
|
| 9 |
A mutation in CTSK gene in an autosomal recessive pycnodysostosis family of Pakistani origin
|
Naeem, Muhammad
|
|
2009
|
10 |
1 |
|
artikel
|
| 10 |
Analyses of associations between three positionally cloned asthma candidate genes and asthma or asthma-related phenotypes in a Chinese population
|
Zhou, Huanyu
|
|
2009
|
10 |
1 |
|
artikel
|
| 11 |
Analysis of TACI mutations in CVID & RESPI patients who have inherited HLA B*44 or HLA*B8
|
Waldrep, Manda L
|
|
2009
|
10 |
1 |
|
artikel
|
| 12 |
A new CYP21A1P/CYP21A2 chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form
|
Concolino, Paola
|
|
2009
|
10 |
1 |
|
artikel
|
| 13 |
An extension to a statistical approach for family based association studies provides insights into genetic risk factors for multiple sclerosis in the HLA-DRB1 gene
|
Ramagopalan, Sreeram V
|
|
2009
|
10 |
1 |
|
artikel
|
| 14 |
An investigation of ribosomal protein L10 gene in autism spectrum disorders
|
Gong, Xiaohong
|
|
2009
|
10 |
1 |
|
artikel
|
| 15 |
An Open Access Database of Genome-wide Association Results
|
Johnson, Andrew D
|
|
2009
|
10 |
1 |
|
artikel
|
| 16 |
A novel c.-22T>C mutation in GALK1 promoter is associated with elevated galactokinase phenotype
|
Park, Hyung-Doo
|
|
2009
|
10 |
1 |
|
artikel
|
| 17 |
A novel study of Copy Number Variations in Hirschsprung disease using the Multiple Ligation-dependent Probe Amplification (MLPA) technique
|
Núñez-Torres, Rocío
|
|
2009
|
10 |
1 |
|
artikel
|
| 18 |
A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS)
|
Castro-Giner, Francesc
|
|
2009
|
10 |
1 |
|
artikel
|
| 19 |
A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness
|
Bardien, Soraya
|
|
2009
|
10 |
1 |
|
artikel
|
| 20 |
Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples
|
Menten, Björn
|
|
2009
|
10 |
1 |
|
artikel
|
| 21 |
Association analyses of the INSIG2 polymorphism in the obesity and cholesterol levels of Korean populations
|
Cha, Seongwon
|
|
2009
|
10 |
1 |
|
artikel
|
| 22 |
Association between ACE gene I/D polymorphisms and hyperandrogenism in women with Polycystic Ovary Syndrome (PCOS) and controls
|
sun, Jing
|
|
2009
|
10 |
1 |
|
artikel
|
| 23 |
Association between a rare SNP in the second intron of human Agouti related protein gene and increased BMI
|
Kalnina, Ineta
|
|
2009
|
10 |
1 |
|
artikel
|
| 24 |
Association between CYP19 gene SNP rs2414096 Polymorphism and polycystic ovary syndrome in Chinese women
|
Jin, Jia-Li
|
|
2009
|
10 |
1 |
|
artikel
|
| 25 |
Association between TCF7L2 gene polymorphisms and susceptibility to Type 2 Diabetes Mellitus: a large Human Genome Epidemiology (HuGE) review and meta-analysis
|
Tong, Yu
|
|
2009
|
10 |
1 |
|
artikel
|
| 26 |
Association of ADAM33 gene polymorphisms with COPD in a northeastern Chinese population
|
Wang, Xinyan
|
|
2009
|
10 |
1 |
|
artikel
|
| 27 |
Association of a de novo 16q copy number variant with a phenotype that overlaps with Lenz microphthalmia and Townes-Brocks syndromes
|
Bardakjian, Tanya M
|
|
2009
|
10 |
1 |
|
artikel
|
| 28 |
Association of a functional microsatellite within intron 1 of the BMP5 gene with susceptibility to osteoarthritis
|
Wilkins, James M
|
|
2009
|
10 |
1 |
|
artikel
|
| 29 |
Association of APOE polymorphism with chronic kidney disease in a nationally representative sample: a Third National Health and Nutrition Examination Survey (NHANES III) Genetic Study
|
Chu, Audrey Y
|
|
2009
|
10 |
1 |
|
artikel
|
| 30 |
Association of DRD4 uVNTR and TP53 codon 72 polymorphisms with schizophrenia: a case-control study
|
Lung, For-Wey
|
|
2009
|
10 |
1 |
|
artikel
|
| 31 |
Association of hypoxia inducible factor-1 alpha gene polymorphism with both type 1 and type 2 diabetes in a Caucasian (Hungarian) sample
|
Nagy, Geza
|
|
2009
|
10 |
1 |
|
artikel
|
| 32 |
Association of vitamin D receptor polymorphisms with the risk of prostate cancer in the Han population of Southern China
|
Bai, Yongheng
|
|
2009
|
10 |
1 |
|
artikel
|
| 33 |
Association study between vitamin D receptor gene polymorphisms and asthma in the chinese han population: a case-control study
|
Saadi, Ahlem
|
|
2009
|
10 |
1 |
|
artikel
|
| 34 |
Association study of SHANK3 gene polymorphisms with autism in Chinese Han population
|
Qin, Jian
|
|
2009
|
10 |
1 |
|
artikel
|
| 35 |
A tagging SNP in INSIG2 is associated with obesity-related phenotypes among Samoans
|
Deka, Ranjan
|
|
2009
|
10 |
1 |
|
artikel
|
| 36 |
Autism genetic database (AGD): a comprehensive database including autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites
|
Matuszek, Gregory
|
|
2009
|
10 |
1 |
|
artikel
|
| 37 |
BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1
|
Brunet, Anna
|
|
2009
|
10 |
1 |
|
artikel
|
| 38 |
Candidate genetic analysis of plasma high-density lipoprotein-cholesterol and severity of coronary atherosclerosis
|
Chen, Suet Nee
|
|
2009
|
10 |
1 |
|
artikel
|
| 39 |
Characterisation of CYP2C8, CYP2C9 and CYP2C19 polymorphisms in a Ghanaian population
|
Kudzi, William
|
|
2009
|
10 |
1 |
|
artikel
|
| 40 |
Common genetic variants of the ion channel transient receptor potential membrane melastatin 6 and 7 (TRPM6 and TRPM7), magnesium intake, and risk of type 2 diabetes in women
|
Song, Yiqing
|
|
2009
|
10 |
1 |
|
artikel
|
| 41 |
Common polymorphisms within the NR4A3 locus, encoding the orphan nuclear receptor Nor-1, are associated with enhanced β-cell function in non-diabetic subjects
|
Weyrich, Peter
|
|
2009
|
10 |
1 |
|
artikel
|
| 42 |
Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitis
|
Carr, Edward J
|
|
2009
|
10 |
1 |
|
artikel
|
| 43 |
Constitutive RB1 mutation in a child conceived by in vitro fertilization: implications for genetic counseling
|
Barbosa, Raquel H
|
|
2009
|
10 |
1 |
|
artikel
|
| 44 |
Contrasting genetic association of IL2RA with SLE and ANCA – associated vasculitis
|
Carr, Edward J
|
|
2009
|
10 |
1 |
|
artikel
|
| 45 |
Contribution of type 2 diabetes associated loci in the Arabic population from Tunisia: a case-control study
|
Ezzidi, Intissar
|
|
2009
|
10 |
1 |
|
artikel
|
| 46 |
Copy-number variation in BMPR2 is not associated with the pathogenesis of pulmonary arterial hypertension
|
Johnson, Jennifer A
|
|
2009
|
10 |
1 |
|
artikel
|
| 47 |
C-Reactive protein gene variants are associated with postoperative C-reactive protein levels after coronary artery bypass surgery
|
Perry, Tjörvi E
|
|
2009
|
10 |
1 |
|
artikel
|
| 48 |
Differentially expressed alternatively spliced genes in Malignant Pleural Mesothelioma identified using massively parallel transcriptome sequencing
|
Dong, Lingsheng
|
|
2009
|
10 |
1 |
|
artikel
|
| 49 |
DNA instability in replicating Huntington's disease lymphoblasts
|
Cannella, Milena
|
|
2009
|
10 |
1 |
|
artikel
|
| 50 |
Do the mutations of C1GALT1C1 gene play important roles in the genetic susceptibility to Chinese IgA nephropathy?
|
Li, Gui-Sen
|
|
2009
|
10 |
1 |
|
artikel
|
| 51 |
DYRK1A genetic variants are not linked to Alzheimer's disease in a Spanish case-control cohort
|
Vázquez-Higuera, José Luis
|
|
2009
|
10 |
1 |
|
artikel
|
| 52 |
Emilin1 gene and essential hypertension: a two-stage association study in northern Han Chinese population
|
Shen, Chong
|
|
2009
|
10 |
1 |
|
artikel
|
| 53 |
Evaluating NAT2PRED for inferring the individual acetylation status from unphased genotype data
|
Sabbagh, Audrey
|
|
2009
|
10 |
1 |
|
artikel
|
| 54 |
Evaluating the association of common APOA2 variants with type 2 diabetes
|
Duesing, Konsta
|
|
2009
|
10 |
1 |
|
artikel
|
| 55 |
Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study
|
Wolf, Christiane
|
|
2009
|
10 |
1 |
|
artikel
|
| 56 |
Evidence for an association of HLA-DRB1*15 and DRB1*09 with leprosy and the impact of DRB1*09 on disease onset in a Chinese Han population
|
Zhang, Furen
|
|
2009
|
10 |
1 |
|
artikel
|
| 57 |
Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2
|
Bernard, Veronica
|
|
2009
|
10 |
1 |
|
artikel
|
| 58 |
Frequency of single nucleotide polymorphisms in NOD1 gene of ulcerative colitis patients: a case-control study in the Indian population
|
Verma, Ravi
|
|
2009
|
10 |
1 |
|
artikel
|
| 59 |
FTO gene variation and measures of body mass in an African population
|
Hennig, Branwen J
|
|
2009
|
10 |
1 |
|
artikel
|
| 60 |
Functional analysis of the C-reactive protein (CRP) gene -717A>G polymorphism associated with coronary heart disease
|
Wang, Laiyuan
|
|
2009
|
10 |
1 |
|
artikel
|
| 61 |
Functional and genetic analysis in type 2 diabetes of Liver X receptor alleles – a cohort study
|
Dahlman, Ingrid
|
|
2009
|
10 |
1 |
|
artikel
|
| 62 |
Functional polymorphism of the NFKB1 gene promoter is related to the risk of dilated cardiomyopathy
|
Zhou, Bin
|
|
2009
|
10 |
1 |
|
artikel
|
| 63 |
Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs
|
Blom, Elin S
|
|
2009
|
10 |
1 |
|
artikel
|
| 64 |
Gastric inhibitory polypeptide receptor: association analyses for obesity of several polymorphisms in large study groups
|
Vogel, Carla IG
|
|
2009
|
10 |
1 |
|
artikel
|
| 65 |
Genetic and other factors determining mannose-binding lectin levels in American Indians: the Strong Heart Study
|
Best, Lyle G
|
|
2009
|
10 |
1 |
|
artikel
|
| 66 |
Genetic association study of selected candidate genes (ApoB, LPL, Leptin) and telomere length in obese and hypertensive individuals
|
Das, Birajalaxmi
|
|
2009
|
10 |
1 |
|
artikel
|
| 67 |
Genetic effect of CysLTR2 polymorphisms on its mRNA synthesis and stabilization
|
Shin, Jeong-Ah
|
|
2009
|
10 |
1 |
|
artikel
|
| 68 |
Genetic variants of the promoter of the heme oxygenase-1 gene and their influence on cardiovascular disease (The Ludwigshafen Risk and Cardiovascular Health Study)
|
Lüblinghoff, Nicola
|
|
2009
|
10 |
1 |
|
artikel
|
| 69 |
Genetic variation in Fcγ receptor IIa and risk of coronary heart disease: negative results from two large independent populations
|
Karakas, Mahir
|
|
2009
|
10 |
1 |
|
artikel
|
| 70 |
Genetic variation in the NBS1, MRE11, RAD50 and BLM genes and susceptibility to non-Hodgkin lymphoma
|
Schuetz, Johanna M
|
|
2009
|
10 |
1 |
|
artikel
|
| 71 |
Genetic variation of NEDD4L is associated with essential hypertension in female Kazakh general population: a case-control study
|
Li, Nanfang
|
|
2009
|
10 |
1 |
|
artikel
|
| 72 |
Genome screen in familial intracranial aneurysm
|
Foroud, Tatiana
|
|
2009
|
10 |
1 |
|
artikel
|
| 73 |
Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis
|
Sha, Qiuying
|
|
2009
|
10 |
1 |
|
artikel
|
| 74 |
Genomewide association study for onset age in Parkinson disease
|
Latourelle, Jeanne C
|
|
2009
|
10 |
1 |
|
artikel
|
| 75 |
Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: The HyperGEN Study
|
Arnett, Donna K
|
|
2009
|
10 |
1 |
|
artikel
|
| 76 |
Haplotype frequencies in a sub-region of chromosome 19q13.3, related to risk and prognosis of cancer, differ dramatically between ethnic groups
|
Schierup, Mikkel H
|
|
2009
|
10 |
1 |
|
artikel
|
| 77 |
HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q
|
Lloyd, Sarah E
|
|
2009
|
10 |
1 |
|
artikel
|
| 78 |
High-throughput mutational analysis of TOR1A in primary dystonia
|
Xiao, Jianfeng
|
|
2009
|
10 |
1 |
|
artikel
|
| 79 |
Homozygosity and risk of childhood death due to invasive bacterial disease
|
Lyons, Emily J
|
|
2009
|
10 |
1 |
|
artikel
|
| 80 |
Identification of a novel functional deletion variant in the 5'-UTR of the DJ-1 gene
|
Keyser, Rowena J
|
|
2009
|
10 |
1 |
|
artikel
|
| 81 |
Identification of a pleiotropic locus on chromosome 7q for a composite left ventricular wall thickness factor and body mass index: the HyperGEN Study
|
Tang, Weihong
|
|
2009
|
10 |
1 |
|
artikel
|
| 82 |
Identification of a region required for TSC1 stability by functional analysis of TSC1 missense mutations found in individuals with tuberous sclerosis complex
|
Mozaffari, Melika
|
|
2009
|
10 |
1 |
|
artikel
|
| 83 |
IL6 and CRP haplotypes are associated with COPD risk and systemic inflammation: a case-control study
|
Yanbaeva, Dilyara G
|
|
2009
|
10 |
1 |
|
artikel
|
| 84 |
IL23R in the Swedish, Finnish, Hungarian and Italian populations: association with IBD and psoriasis, and linkage to celiac disease
|
Einarsdottir, Elisabet
|
|
2009
|
10 |
1 |
|
artikel
|
| 85 |
Influences of polymorphic variants of DRD2 and SLC6A3 genes, and their combinations on smoking in Polish population
|
Sieminska, Alicja
|
|
2009
|
10 |
1 |
|
artikel
|
| 86 |
Innate immunity in ocular Chlamydia trachomatis infection: contribution of IL8 and CSF2 gene variants to risk of trachomatous scarring in Gambians
|
Natividad, Angels
|
|
2009
|
10 |
1 |
|
artikel
|
| 87 |
Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels
|
Domanska, Katarina
|
|
2009
|
10 |
1 |
|
artikel
|
| 88 |
Lack of association between polymorphisms of the IL18R1 and IL18RAP genes and cardiovascular risk: the MORGAM Project
|
Grisoni, Marie-Lise
|
|
2009
|
10 |
1 |
|
artikel
|
| 89 |
Lack of association between PRNP 1368 polymorphism and Alzheimer's disease or vascular dementia
|
Jeong, Byung-Hoon
|
|
2009
|
10 |
1 |
|
artikel
|
| 90 |
Lack of association of TIM3 polymorphisms and allergic phenotypes
|
Zhang, Jian
|
|
2009
|
10 |
1 |
|
artikel
|
| 91 |
Locations and patterns of meiotic recombination in two-generation pedigrees
|
Ting, Jason C
|
|
2009
|
10 |
1 |
|
artikel
|
| 92 |
Low frequency of the TIRAP S180L polymorphism in Africa, and its potential role in malaria, sepsis, and leprosy
|
Hamann, Lutz
|
|
2009
|
10 |
1 |
|
artikel
|
| 93 |
Melusin gene (ITGB1BP2) nucleotide variations study in hypertensive and cardiopathic patients
|
Palumbo, Valeria
|
|
2009
|
10 |
1 |
|
artikel
|
| 94 |
Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations
|
Mocci, Evelina
|
|
2009
|
10 |
1 |
|
artikel
|
| 95 |
Mild forms of hypophosphatasia mostly result from dominant negative effect of severe alleles or from compound heterozygosity for severe and moderate alleles
|
Fauvert, Delphine
|
|
2009
|
10 |
1 |
|
artikel
|
| 96 |
Mitochondrial DNA haplogroup T is associated with coronary artery disease and diabetic retinopathy: a case control study
|
Kofler, Barbara
|
|
2009
|
10 |
1 |
|
artikel
|
| 97 |
Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia
|
Alsmadi, Osama
|
|
2009
|
10 |
1 |
|
artikel
|
| 98 |
Molecular analysis of the APC and MUTYH genes in Galician and Catalonian FAP families: a different spectrum of mutations?
|
Gómez-Fernández, Nuria
|
|
2009
|
10 |
1 |
|
artikel
|
| 99 |
Mosaicism for combined tetrasomy of chromosomes 8 and 18 in a dysmorphic child: A result of failed tetraploidy correction?
|
Houge, Gunnar
|
|
2009
|
10 |
1 |
|
artikel
|
| 100 |
Multiple splice defects in ABCA1 cause low HDL-C in a family with Hypoalphalipoproteinemia and premature coronary disease
|
Rhyne, Jeffrey
|
|
2009
|
10 |
1 |
|
artikel
|
| 101 |
Mutation analysis of "Endoglin" and "Activin receptor-like kinase" genes in German patients with hereditary hemorrhagic telangiectasia and the value of rapid genotyping using an allele-specific PCR-technique
|
Haneen, Sadick
|
|
2009
|
10 |
1 |
|
artikel
|
| 102 |
Mutations in STK11 gene in Czech Peutz-Jeghers patients
|
Vasovčák, Peter
|
|
2009
|
10 |
1 |
|
artikel
|
| 103 |
New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease
|
Stekrova, Jitka
|
|
2009
|
10 |
1 |
|
artikel
|
| 104 |
Nitric oxide synthase 2A (NOS2A) polymorphisms are not associated with invasive pneumococcal disease
|
Payton, Antony
|
|
2009
|
10 |
1 |
|
artikel
|
| 105 |
No association of CDK5 genetic variants with Alzheimer's disease risk
|
Vázquez-Higuera, José Luis
|
|
2009
|
10 |
1 |
|
artikel
|
| 106 |
Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry
|
Vogel, Carla IG
|
|
2009
|
10 |
1 |
|
artikel
|
| 107 |
No relationship between 2',3'-cyclic nucleotide 3'-phosphodiesterase and schizophrenia in the Chinese Han population: an expression study and meta-analysis
|
Che, Ronglin
|
|
2009
|
10 |
1 |
|
artikel
|
| 108 |
Novel quantitative trait locus is mapped to chromosome 12p11 for left ventricular mass in Dominican families: the Family Study of Stroke Risk and Carotid Atherosclerosis
|
Wang, Liyong
|
|
2009
|
10 |
1 |
|
artikel
|
| 109 |
OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background
|
Pierron, Denis
|
|
2009
|
10 |
1 |
|
artikel
|
| 110 |
Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions
|
Casselbrant, Margaretha L
|
|
2009
|
10 |
1 |
|
artikel
|
| 111 |
Parental diabetes status reveals association of mitochondrial DNA haplogroup J1 with type 2 diabetes
|
Feder, Jeanette
|
|
2009
|
10 |
1 |
|
artikel
|
| 112 |
Pathogenesis of vestibular schwannoma in ring chromosome 22
|
Denayer, Ellen
|
|
2009
|
10 |
1 |
|
artikel
|
| 113 |
PIN1 gene variants in Alzheimer's disease
|
Maruszak, Aleksandra
|
|
2009
|
10 |
1 |
|
artikel
|
| 114 |
PLAUR polymorphisms and lung function in UK smokers
|
Stewart, Ceri E
|
|
2009
|
10 |
1 |
|
artikel
|
| 115 |
PLCL1 rs7595412 variation is not associated with hip bone size variation in postmenopausal Danish women
|
Cauchi, Stéphane
|
|
2009
|
10 |
1 |
|
artikel
|
| 116 |
Polymorphisms in the ADRB2 gene and Graves disease: a case-control study and a meta-analysis of available evidence
|
Chu, Xun
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2009
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10 |
1 |
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artikel
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| 117 |
Power of multifactor dimensionality reduction and penalized logistic regression for detecting gene-gene Interaction in a case-control study
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He, Hua
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2009
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10 |
1 |
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artikel
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| 118 |
PPARγ Pro12Ala polymorphism and risk of acute coronary syndrome in a prospective study of Danes
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Vogel, Ulla
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2009
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10 |
1 |
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artikel
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| 119 |
Prevalence of pathogenetic MC4R mutations in Italian children with early Onset obesity, tall stature and familial history of obesity
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Santoro, Nicola
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2009
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10 |
1 |
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artikel
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| 120 |
PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism
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Bishop, Matthew T
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2009
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10 |
1 |
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artikel
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| 121 |
Rapid detection of the CYP2A6*12 hybrid allele by Pyrosequencing® technology
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Koontz, Deborah A
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2009
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10 |
1 |
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artikel
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| 122 |
Rapid diagnosis of spinal muscular atrophy using High-Resolution Melting Analysis
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Chen, Wan Jin
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2009
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10 |
1 |
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artikel
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| 123 |
Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients
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Masotti, Cibele
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2009
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10 |
1 |
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artikel
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| 124 |
Relationship of circulating cell-free DNA levels to cell-free fetal DNA levels, clinical characteristics and laboratory parameters in preeclampsia
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Lazar, Levente
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2009
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10 |
1 |
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artikel
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| 125 |
Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia
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Marjamaa, Annukka
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2009
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10 |
1 |
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artikel
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| 126 |
Single nucleotide polymorphisms in obesity-related genes and all-cause and cause-specific mortality: a prospective cohort study
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Gallicchio, Lisa
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2009
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10 |
1 |
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artikel
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| 127 |
SLC6A3 and body mass index in the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial
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Azzato, Elizabeth M
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2009
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10 |
1 |
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artikel
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| 128 |
118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects
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Shaw, Gary M
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2009
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10 |
1 |
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artikel
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| 129 |
STK39 polymorphisms and blood pressure: an association study in British Caucasians and assessment of cis-acting influences on gene expression
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Cunnington, Michael S
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2009
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10 |
1 |
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artikel
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| 130 |
Studies of CTNNBL1 and FDFT1 variants and measures of obesity: analyses of quantitative traits and case-control studies in 18,014 Danes
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Andreasen, Camilla Helene
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2009
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10 |
1 |
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artikel
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| 131 |
Suggestion for linkage of chromosome 1p35.2 and 3q28 to plasma adiponectin concentrations in the GOLDN Study
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Rasmussen-Torvik, Laura J
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2009
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10 |
1 |
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artikel
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| 132 |
Suggestive linkage detected for blood pressure related traits on 2q and 22q in the population on the Samoan islands
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Åberg, Karolina
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2009
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10 |
1 |
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artikel
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| 133 |
Telomere shortening may be associated with human keloids
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De Felice, Bruna
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2009
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10 |
1 |
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artikel
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| 134 |
The common FTO variant rs9939609 is not associated with BMI in a longitudinal study on a cohort of Swedish men born 1920-1924
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Jacobsson, Josefin A
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2009
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10 |
1 |
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artikel
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| 135 |
The first Dutch SDHB founder deletion in paraganglioma – pheochromocytoma patients
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Bayley, Jean-Pierre
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2009
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10 |
1 |
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artikel
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| 136 |
The INSIG2 rs7566605 genetic variant does not play a major role in obesity in a sample of 24,722 individuals from four cohorts
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Bressler, Jan
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2009
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10 |
1 |
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artikel
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| 137 |
The mitochondrial DNA T16189C polymorphism and HIV-associated cardiomyopathy: a genotype-phenotype association study
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Shaboodien, Gasnat
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2009
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10 |
1 |
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artikel
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| 138 |
The multidrug resistance 1 (MDR1) gene polymorphism G-rs3789243-A is not associated with disease susceptibility in Norwegian patients with colorectal adenoma and colorectal cancer; a case control study
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Andersen, Vibeke
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2009
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10 |
1 |
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artikel
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| 139 |
The neck-region polymorphism of DC-SIGNR in peri-centenarian from Han Chinese Population
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Li, Hui
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2009
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10 |
1 |
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artikel
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| 140 |
The promoter polymorphism -232C/G of the PCK1 gene is associated with type 2 diabetes in a UK-resident South Asian population
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Rees, Simon D
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2009
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10 |
1 |
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artikel
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| 141 |
The role of CACNA1S in predisposition to malignant hyperthermia
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Carpenter, Danielle
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2009
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10 |
1 |
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artikel
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| 142 |
The rs1990760 polymorphism within the IFIH1 locus is not associated with Graves' disease, Hashimoto's thyroiditis and Addison's disease
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Penna-Martinez, Marissa
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|
2009
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10 |
1 |
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artikel
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| 143 |
Two-stage case-control association study of dopamine-related genes and migraine
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Corominas, Roser
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2009
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10 |
1 |
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artikel
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| 144 |
Type 2 diabetes gene TCF7L2 polymorphism is not associated with fetal and postnatal growth in two birth cohort studies
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Mook-Kanamori, Dennis O
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2009
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10 |
1 |
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artikel
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| 145 |
Unambiguous molecular detections with multiple genetic approach for the complicated chromosome 22q11 deletion syndrome
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Yang, Chen
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2009
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10 |
1 |
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artikel
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| 146 |
Use of supplementary phenotype to identify additional rheumatoid arthritis loci in a linkage analysis of 342 UK affected sibling pair families
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Tayo, Bamidele O
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2009
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10 |
1 |
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artikel
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| 147 |
Variation in cytokine genes can contribute to severity of acetabular osteolysis and risk for revision in patients with ABG 1 total hip arthroplasty: a genetic association study
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Gallo, Jiri
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2009
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10 |
1 |
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artikel
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| 148 |
Variation in the UCP2 and UCP3 genes associates with abdominal obesity and serum lipids: The Finnish Diabetes Prevention Study
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Salopuro, Titta
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2009
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10 |
1 |
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artikel
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| 149 |
Voltage-dependent anion channel (VDAC) is involved in apoptosis of cell lines carrying the mitochondrial DNA mutation
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Yuqi, Liu
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2009
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10 |
1 |
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artikel
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