Lista de obras - Frank Geller - Dominio Público Uruguay

5-HT2A promoter polymorphism -1438G/A in children and adolescents with obsessive-compulsive disorders

artículo científico publicado en 2002

A bivariate Haseman-Elston method and application to the analysis of asthma-related phenotypes on chromosome 5q.

artículo científico publicado en 2001

A novel common variant in DCST2 is associated with length in early life and height in adulthood

artículo científico publicado en 2014

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

artículo científico publicado en 2008

Absence of the wild-type allele (192 base pairs) of a polymorphism in the promoter region of the IGF-I gene but not a polymorphism in the insulin gene variable number of tandem repeat locus is associated with accelerated weight gain in infancy

artículo científico publicado en 2006

Addictions and their familiality in Iceland

artículo científico publicado en 2010

Association of the 103I MC4R allele with decreased body mass in 7937 participants of two population based surveys

artículo científico publicado en 2005

Binge-eating episodes are not characteristic of carriers of melanocortin-4 receptor gene mutations

artículo científico publicado en 2004

Bladder cancer and occupational exposures in North Rhine-Westphalia, Germany

artículo científico publicado en 2008

Brain-derived neurotrophic factor V66M polymorphism in childhood-onset obsessive-compulsive disorder

artículo científico publicado en 2005

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

artículo científico publicado en 2017

CPT1A Missense Mutation Associated With Fatty Acid Metabolism and Reduced Height in Greenlanders

artículo científico publicado en 2017

Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa

artículo científico publicado en 2004

Common variants associated with general and MMR vaccine-related febrile seizures

artículo científico publicado en 2014

Common variants at 12q15 and 12q24 are associated with infant head circumference

artículo científico publicado en 2012

Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis

artículo científico publicado en 2012

Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits

artículo científico publicado en 2008

Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations

artículo científico publicado en 2009

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer

artículo científico publicado en 2007

Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis

artículo científico publicado en 2016

Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

artículo científico publicado en 2022

Consortium genome-wide meta-analysis for childhood dental caries traits

Consortium-based genome-wide meta-analysis for childhood dental caries traits

scholarly article by Simon Haworth published in September 2018

Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2016

Defining the role of common variation in the genomic and biological architecture of adult human height

artículo científico publicado en 2014

Detection rates for genotyping errors in SNPs using the trio design

artículo científico publicado en 2002

Determination of NAT2 acetylation status in the Greenlandic population

artículo científico publicado en 2015

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

Dopamine receptor gene polymorphisms in Parkinson's disease patients reporting "sleep attacks".

artículo científico publicado en 2004

Elevated bladder cancer risk due to colorants--a statewide case-control study in North Rhine-Westphalia, Germany

artículo científico

Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference

scholarly article published in Nature Genetics

Evaluation of BMP4 and its specific inhibitor NOG as candidates in human neural tube defects (NTDs)

GSTP1 A1578G (Ile105Val) polymorphism in benzidine-exposed workers: an association with cytological grading of exfoliated urothelial cells

artículo científico publicado en 2003

GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI

artículo científico publicado en 2019

Genetic Associations with Gestational Duration and Spontaneous Preterm Birth

artículo científico publicado en 2017

Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight

artículo científico publicado en 2016

Genetic architecture of early childhood growth phenotypes gives insights into their link with later obesity

Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

scientific article published on 25 November 2020

Genetic predisposition to obesity in bulimia nervosa: a mutation screen of the melanocortin-4 receptor gene

article

Genetic studies of body mass index yield new insights for obesity biology

artículo científico publicado en 2015

Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight

artículo científico publicado en 2012

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

artículo científico publicado en 2018

Genome scan for body mass index and height in the Framingham Heart Study

artículo científico publicado en 2003

Genome scan for childhood and adolescent obesity in German families

artículo científico publicado en 2003

Genome-wide association analyses identify variants in developmental genes associated with hypospadias

artículo científico publicado en 2014

Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index

artículo científico publicado en 2015

Genome-wide association scan for childhood caries implicates novel genes

scientific journal article

Genome-wide association study identifies 48 common genetic variants associated with handedness

artículo científico publicado en 2020

Genome-wide association study identifies four loci associated with eruption of permanent teeth

artículo científico publicado en 2011

Genome-wide association study identifies variants in HORMAD2 associated with tonsillectomy

artículo científico publicado en 2016

Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus

artículo científico publicado en 2018

Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics

article

Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

artículo científico publicado en 2018

Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances

artículo científico publicado en 2013

Genome-wide associations for birth weight and correlations with adult disease

artículo científico publicado en 2016

Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis

artículo científico publicado en 2019

Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption

artículo científico publicado en 2014

Ghrelin gene: identification of missense variants and a frameshift mutation in extremely obese children and adolescents and healthy normal weight students

artículo científico publicado en 2002

Ghrelin receptor gene: identification of several sequence variants in extremely obese children and adolescents, healthy normal-weight and underweight students, and children with short normal stature

artículo científico publicado en 2004

Glucose transporter 4 gene: association studies pertaining to alleles of two polymorphisms in extremely obese children and adolescents and in normal and underweight controls.

artículo científico publicado en 2002

Human galanin (GAL) and galanin 1 receptor (GALR1) variations are not involved in fat intake and early onset obesity

artículo científico publicado en 2005

Increased body mass index (BMI) in male narcoleptic patients, but not in HLA-DR2-positive healthy male volunteers

artículo científico publicado en 2002

Increased body-mass index in patients with narcolepsy.

artículo científico publicado en 2000

Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology

artículo científico publicado en 2013

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

artículo científico publicado en 2012

Independent confirmation of a major locus for obesity on chromosome 10.

artículo científico publicado en 2000

Lack of support for the association between GAD2 polymorphisms and severe human obesity

artículo científico publicado en 2005

Large quantitative effect of melanocortin-4 receptor gene mutations on body mass index

artículo científico publicado en 2004

Lower serum leptin levels in female students of the nutritional sciences with eating disorders

artículo científico publicado en 2003

Male-pattern baldness susceptibility locus at 20p11.

artículo científico publicado en 2008

Maternal and fetal genetic contribution to gestational weight gain

article

Maternal and fetal genetic contribution to gestational weight gain.

artículo científico publicado en 2017

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

Melanocortin-4 receptor gene variant I103 is negatively associated with obesity

artículo científico publicado en 2004

Melanocortin-4 receptor gene: case-control study and transmission disequilibrium test confirm that functionally relevant mutations are compatible with a major gene effect for extreme obesity.

artículo científico publicado en 2003

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

artículo científico publicado en 2012

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

artículo científico publicado en 2015

Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.

artículo científico publicado en 2017

Mutation analysis of the MCHR1 gene in human obesity

artículo científico publicado en 2005

Mutation screen of the brain derived neurotrophic factor gene (BDNF): Identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention-deficit/hyperactivity disorder

article

N-Acetyltransferase 1 in Colon and Rectal Cancer Cases from an Industrialized Area

N-Acetyltransferase 2 and glutathione s-transferase M1 in colon and rectal cancer cases from an industrialized area

artículo científico

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

artículo científico publicado en 2012

No association between age at menarche and sex of offspring

No evidence for involvement of alleles of the 825-C/T polymorphism of the G-protein subunit beta 3 in body weight regulation

artículo científico publicado en 2001

No evidence for involvement of the calpain-10 gene `high-risk' haplotype combination for non-insulin-dependent diabetes mellitus in early onset obesity

article

No evidence for involvement of the promoter polymorphism -866 G/A of the UCP2 gene in childhood-onset obesity in humans.

artículo científico publicado en 2003

No observed association for mitochondrial SNPs with preterm delivery and related outcomes

artículo científico publicado en 2012

On the total expected study cost in two-stage genome-wide search designs for linkage analysis using the mean test for affected sib pairs

article

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

artículo científico publicado en 2014

Perspectives: molecular genetic research in human obesity

artículo científico publicado en 2003

Perzentile für den Body-mass-Index für das Kindes- und Jugendalter unter Heranziehung verschiedener deutscher Stichproben

article by K. Kromeyer-Hauschild et al published August 2001 in Monatsschrift Kinderheilkunde

Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis

scientific journal article

Possible genomic imprinting of three human obesity-related genetic loci

artículo científico publicado en 2005

Preprohypocretin polymorphisms in Parkinson disease patients reporting "sleep attacks".

artículo científico publicado en 2005

Prevalence of obesity in adolescent and young adult patients with and without schizophrenia and in relationship to antipsychotic medication

artículo científico publicado en 2001

Rare and Common Variants Conferring Risk of Tooth Agenesis.

artículo científico publicado en 2018

Replication of a genome-wide association study of birth weight in preterm neonates

artículo científico publicado en 2011

Secular trends in body mass index measurements in preschool children from the City of Aachen, Germany

artículo científico publicado en 2003

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

artículo científico publicado en 2008

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

artículo científico publicado en 2010

Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption

artículo científico publicado en 2011

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

artículo científico publicado en 2009

Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study

artículo científico publicado en 2013

Serotonergic effects of clozapine and its metabolites in hippocampal HT22 cells

artículo científico publicado en 2002

Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases

artículo científico publicado en 2012

Study of correlation between the NAT2 phenotype and genotype status among Greenlandic Inuit

The 103I variant of the melanocortin 4 receptor is associated with low serum triglyceride levels

artículo científico publicado en 2005

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2015

The genetics of obesity: practical implications

article

The use of sequential designs in genome scans for asthma susceptibility loci with affected sib pairs

artículo científico publicado en 2001

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

artículo científico publicado en 2010

Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorder

artículo científico publicado en 2005

Transmission disequilibrium studies in children and adolescents with obsessive-compulsive disorders pertaining to polymorphisms of genes of the serotonergic pathway

artículo científico publicado en 2004

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

article

X-chromosomal maternal and fetal SNPs and the risk of spontaneous preterm delivery in a Danish/Norwegian genome-wide association study

artículo científico publicado en 2013

Lista de obras de Frank Geller

5-HT2A promoter polymorphism -1438G/A in children and adolescents with obsessive-compulsive disorders

A bivariate Haseman-Elston method and application to the analysis of asthma-related phenotypes on chromosome 5q.

A novel common variant in DCST2 is associated with length in early life and height in adulthood

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

Absence of the wild-type allele (192 base pairs) of a polymorphism in the promoter region of the IGF-I gene but not a polymorphism in the insulin gene variable number of tandem repeat locus is associated with accelerated weight gain in infancy

Addictions and their familiality in Iceland

Association of the 103I MC4R allele with decreased body mass in 7937 participants of two population based surveys

Binge-eating episodes are not characteristic of carriers of melanocortin-4 receptor gene mutations

Bladder cancer and occupational exposures in North Rhine-Westphalia, Germany

Brain-derived neurotrophic factor V66M polymorphism in childhood-onset obsessive-compulsive disorder

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

CPT1A Missense Mutation Associated With Fatty Acid Metabolism and Reduced Height in Greenlanders

Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa

Common variants associated with general and MMR vaccine-related febrile seizures

Common variants at 12q15 and 12q24 are associated with infant head circumference

Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis

Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits

Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer

Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis

Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

Consortium genome-wide meta-analysis for childhood dental caries traits

Consortium-based genome-wide meta-analysis for childhood dental caries traits

Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

Defining the role of common variation in the genomic and biological architecture of adult human height

Detection rates for genotyping errors in SNPs using the trio design

Determination of NAT2 acetylation status in the Greenlandic population

Directional dominance on stature and cognition in diverse human populations

Dopamine receptor gene polymorphisms in Parkinson's disease patients reporting "sleep attacks".

Elevated bladder cancer risk due to colorants--a statewide case-control study in North Rhine-Westphalia, Germany

Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference

Evaluation of BMP4 and its specific inhibitor NOG as candidates in human neural tube defects (NTDs)

GSTP1 A1578G (Ile105Val) polymorphism in benzidine-exposed workers: an association with cytological grading of exfoliated urothelial cells

GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI

Genetic Associations with Gestational Duration and Spontaneous Preterm Birth

Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight

Genetic architecture of early childhood growth phenotypes gives insights into their link with later obesity

Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

Genetic predisposition to obesity in bulimia nervosa: a mutation screen of the melanocortin-4 receptor gene

Genetic studies of body mass index yield new insights for obesity biology

Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

Genome scan for body mass index and height in the Framingham Heart Study

Genome scan for childhood and adolescent obesity in German families

Genome-wide association analyses identify variants in developmental genes associated with hypospadias

Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index

Genome-wide association scan for childhood caries implicates novel genes

Genome-wide association study identifies 48 common genetic variants associated with handedness

Genome-wide association study identifies four loci associated with eruption of permanent teeth

Genome-wide association study identifies variants in HORMAD2 associated with tonsillectomy

Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus

Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics

Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances

Genome-wide associations for birth weight and correlations with adult disease

Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis

Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption

Ghrelin gene: identification of missense variants and a frameshift mutation in extremely obese children and adolescents and healthy normal weight students

Ghrelin receptor gene: identification of several sequence variants in extremely obese children and adolescents, healthy normal-weight and underweight students, and children with short normal stature

Glucose transporter 4 gene: association studies pertaining to alleles of two polymorphisms in extremely obese children and adolescents and in normal and underweight controls.

Human galanin (GAL) and galanin 1 receptor (GALR1) variations are not involved in fat intake and early onset obesity

Increased body mass index (BMI) in male narcoleptic patients, but not in HLA-DR2-positive healthy male volunteers

Increased body-mass index in patients with narcolepsy.

Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

Independent confirmation of a major locus for obesity on chromosome 10.

Lack of support for the association between GAD2 polymorphisms and severe human obesity

Large quantitative effect of melanocortin-4 receptor gene mutations on body mass index

Lower serum leptin levels in female students of the nutritional sciences with eating disorders

Male-pattern baldness susceptibility locus at 20p11.

Maternal and fetal genetic contribution to gestational weight gain

Maternal and fetal genetic contribution to gestational weight gain.

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

Melanocortin-4 receptor gene variant I103 is negatively associated with obesity

Melanocortin-4 receptor gene: case-control study and transmission disequilibrium test confirm that functionally relevant mutations are compatible with a major gene effect for extreme obesity.

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.

Mutation analysis of the MCHR1 gene in human obesity