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List of works by Frank Geller

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

scientific article published in January 2002

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

scientific article published in January 2001

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

scientific article published on 3 October 2014

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

scientific article (publication date: 3 April 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

scientific article published in December 2006

Addictions and their familiality in Iceland

scientific article

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

scientific article published in April 2005

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

scientific article published in August 2004

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

scientific article published in January 2008

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

scientific article published on 10 January 2005

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

scientific article published on 29 September 2017

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

scientific article published on June 2017

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

scientific article published in January 2004

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

scientific article published on 26 October 2014

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

scientific article published on 15 April 2012

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

scientific article published on 05 February 2012

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

scientific article published on 12 October 2008

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

scientific article published on 6 February 2009

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

scientific article

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

scientific article published on 25 July 2016

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

scientific article published on 09 June 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

scientific article

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

scientific article

Detection rates for genotyping errors in SNPs using the trio design

scientific article published in January 2002

Determination of NAT2 acetylation status in the Greenlandic population

scientific article published on 21 March 2015

Directional dominance on stature and cognition in diverse human populations

scientific article published in July 2015

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

scientific article published in November 2004

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

scientific article published on January 2008

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

scientific article published in July 2003

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

scientific article published on 04 September 2019

Genetic Associations with Gestational Duration and Spontaneous Preterm Birth

scientific article published on 6 September 2017

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

scientific article published on March 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

scientific article

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

scientific article

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

scientific article published in November 2018

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

scientific article

Genome scan for childhood and adolescent obesity in German families

scientific article published in February 2003

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

scientific article published on 10 August 2014

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

scientific article published on 24 November 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

scientific article published on 28 September 2020

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

scientific article

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

scientific article published on 9 December 2016

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

scientific article

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

scientific article published on 3 January 2018

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

scientific article published on 23 May 2013

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

scientific article

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

scientific article published on 01 January 2019

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

scientific article

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

scientific article published in June 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

scientific article

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

scientific article

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

scientific article

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

scientific article published in July 2002

Increased body-mass index in patients with narcolepsy.

scientific article

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

scientific article

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

scientific article

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

scientific article published in August 2000

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

scientific article published on 30 August 2005

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

scientific article published in October 2004

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

scientific article published in June 2003

Male-pattern baldness susceptibility locus at 20p11.

scientific article

Maternal and fetal genetic contribution to gestational weight gain

article

Maternal and fetal genetic contribution to gestational weight gain.

scientific article published on 9 October 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

scientific article

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.

scientific article

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

scientific article

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

scientific article published on 19 October 2015

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

scientific article published on 22 December 2017

Mutation analysis of the MCHR1 gene in human obesity

scientific article published in June 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

scientific article published on January 2012

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

scientific article published on 2 December 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

scientific article published in January 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.

scientific article

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

scientific article published on 17 August 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

scientific article

Perspectives: molecular genetic research in human obesity

scientific article

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

scientific article

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

scientific article published in July 2005

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

scientific article

Rare and Common Variants Conferring Risk of Tooth Agenesis.

scientific article

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

scientific article published on 31 August 2011

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

scientific article published on 9 January 2003

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

scientific article

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

scientific article

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

scientific article

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

scientific article (publication date: February 2009)

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

scientific article

Serotonergic effects of clozapine and its metabolites in hippocampal HT22 cells

scientific article

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

scientific article

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

scientific article published on 8 November 2005

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

scientific article

The genetics of obesity: practical implications

article

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

scientific article published in January 2001

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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