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Lista de obras de Struan F.A. Grant

17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestry

article

3D promoter architecture re-organization during iPSC-derived neuronal cell differentiation implicates target genes for neurodevelopmental disorders

artículo científico publicado en 2021

A ChIP-seq-defined genome-wide map of MEF2C binding reveals inflammatory pathways associated with its role in bone density determination.

artículo científico publicado en 2013

A Dementia-Associated Risk Variant near TMEM106B Alters Chromatin Architecture and Gene Expression.

artículo científico publicado en 2017

A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites.

artículo científico publicado en 2017

A Global Perspective of Latent Autoimmune Diabetes in Adults

artículo científico publicado en 2018

A Unified Pathophysiological Construct of Diabetes and its Complications

artículo científico publicado en 2017

A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls.

artículo científico publicado en 2013

A genome-wide association meta-analysis identifies new childhood obesity loci

artículo científico publicado en 2012

A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.

artículo científico publicado en 2016

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

artículo científico publicado en 2007

A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.

artículo científico publicado en 2009

A genome-wide association study on obesity and obesity-related traits

artículo científico publicado en 2011

A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci

scientific journal article

A genome-wide study reveals copy number variants exclusive to childhood obesity cases

artículo científico publicado en 2010

A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry

artículo científico publicado en 2013

A meta-analysis of the transferability of bone mineral density genetic loci associations from European to African ancestry populations

artículo científico publicado en 2020

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

artículo científico publicado en 2014

A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study

artículo científico publicado en 2008

A trans-ethnic genome-wide association study identifies gender-specific loci influencing pediatric aBMD and BMC at the distal radius.

artículo científico publicado en 2015

ATOM: a powerful gene-based association test by combining optimally weighted markers

artículo científico publicado en 2008

Advances in Whole Genome Sequencing Technology ⬇️

artículo científico publicado el 1 de febrero de 2011

Allelic expression imbalance: tipping the scales to elucidate the function of type 2 diabetes-associated loci.

artículo científico publicado en 2015

An Sp1 Binding Site Polymorphism in the COLIA1 Gene Predicts Osteoporotic Fractures in Both Men and Women ⬇️

artículo científico publicado el 1 de septiembre de 1998

Association Between Linear Growth and Bone Accrual in a Diverse Cohort of Children and Adolescents

artículo científico publicado en 2017

Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP.

artículo científico publicado en 2008

Association analysis of type 2 diabetes Loci in type 1 diabetes.

artículo científico publicado en 2008

Association between a high-risk autism locus on 5p14 and social communication spectrum phenotypes in the general population

artículo científico publicado en 2010

Association of RASGRP1 with type 1 diabetes is revealed by combined follow-up of two genome-wide studies.

artículo científico publicado en 2009

Association of TCF7L2 variation with single islet autoantibody expression in children with type 1 diabetes

artículo científico publicado en 2014

Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry.

artículo científico publicado en 2009

Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's disease

artículo científico publicado en 2007

Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis

scientific article published on 01 July 2008

Association of variants of the interleukin-23 receptor gene with susceptibility to pediatric Crohn's disease

artículo científico publicado en 2007

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

artículo científico publicado en 2009

BMD-associated variation at the Osterix locus is correlated with childhood obesity in females

artículo científico publicado en 2011

Body mass index (BMI) trajectories in infancy differ by population ancestry and may presage disparities in early childhood obesity

artículo científico publicado en 2015

CRISPR-Cas9-Mediated Genome Editing Confirms <i>EPDR1</i> as an Effector Gene at the BMD GWAS-Implicated '<i>STARD3NL</i>' Locus

artículo científico publicado en 2021

Can the genetics of type 1 and type 2 diabetes shed light on the genetics of latent autoimmune diabetes in adults?

artículo científico publicado en 2009

Characterization of the transcriptional machinery bound across the widely presumed type 2 diabetes causal variant, rs7903146, within TCF7L2.

artículo científico publicado en 2014

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma

artículo científico publicado en 2008

Cis-regulatory architecture of human ESC-derived hypothalamic neuron differentiation aids in variant-to-gene mapping of relevant complex traits

artículo científico publicado en 2021

Collagen Iα1 Sp1 Polymorphism, Bone Mass, and Bone Turnover in Healthy French Premenopausal Women: The OFELY Study ⬇️

artículo científico publicado el 1 de mayo de 1998

Colorectal Cancer-Associated Smad4 R361 Hotspot Mutations Boost Wnt/β-Catenin Signaling through Enhanced Smad4-LEF1 Binding

artículo científico publicado en 2021

Common genetic variants on 5p14.1 associate with autism spectrum disorders

artículo científico publicado en 2009

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

artículo científico publicado en 2012

Common variants at 5q22 associate with pediatric eosinophilic esophagitis

scientific journal article

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

artículo científico publicado en 2009

Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects

artículo científico publicado en 2010

Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals

artículo científico publicado en 2015

Contribution of the collagen I alpha1 and vitamin D receptor genes to the risk of hip fracture in elderly women.

artículo científico publicado en 2005

Copy number variation at 1q21.1 associated with neuroblastoma

artículo científico publicado en 2009

Copy number variation on chromosome 10q26.3 for obesity identified by a genome-wide study

artículo científico publicado en 2012

Copy number variations in alternative splicing gene networks impact lifespan

artículo científico publicado en 2013

Correction: A Genome-Wide Association Study on Obesity and Obesity-Related Traits.

artículo científico publicado en 2012

DNA binding by FOXP3 domain-swapped dimer suggests mechanisms of long-range chromosomal interactions.

artículo científico publicado en 2015

Developmental origins of genotype-phenotype correlations in chronic diseases of old age.

artículo científico publicado en 2012

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.

artículo científico publicado en 2017

Dissecting heterogeneity in paediatric Type 1 diabetes: association of TCF7L2 rs7903146 TT and low-risk human leukocyte antigen (HLA) genotypes.

artículo científico publicado en 2016

Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease

artículo científico publicado en 2009

Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder

artículo científico publicado en 2010

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

article by Matthew B. Lanktree et al published June 2012 in American Journal of Human Genetics

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

scholarly article published in Nature Genetics

Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume

article

Ethnic disparities in DNA methylation and risk of type 2 diabetes.

artículo científico publicado en 2015

Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI.

artículo científico publicado en 2009

Examination of genetic variants influencing lipid traits in pediatric populations.

artículo científico publicado en 2012

Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene.

artículo científico publicado en 2009

FGF21 deficiency is associated with childhood obesity, insulin resistance and hypoadiponectinaemia: The BCAMS Study

artículo científico publicado en 2017

First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes

artículo científico publicado en 2018

Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes

artículo científico publicado en 2008

From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes.

artículo científico publicado en 2009

GATA factors promote ER integrity and β-cell survival and contribute to type 1 diabetes risk.

artículo científico publicado en 2013

GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children ⬇️

artículo científico publicado el 20 de diciembre de 2012

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

artículo científico publicado en 2019

Generation of High Quality Chromatin Immunoprecipitation DNA Template for High-throughput Sequencing (ChIP-seq) ⬇️

artículo científico publicado el 19 de abril de 2013

Genes and osteoporosis

scientific article published on 01 August 1997

Genetic Determinants of Childhood Obesity

scientific article published on 01 October 2020

Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC

scientific article published on 16 December 2019

Genetic Risk Scores Implicated in Adult Bone Fragility Associate With Pediatric Bone Density.

artículo científico publicado en 2015

Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans.

artículo científico publicado en 2010

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

artículo científico publicado en 2011

Genetic sharing and heritability of paediatric age of onset autoimmune diseases.

artículo científico publicado en 2015

Genetic susceptibility to type 2 diabetes and obesity: follow-up of findings from genome-wide association studies.

artículo científico publicado en 2014

Genetic variation in genes encoding airway epithelial potassium channels is associated with chronic rhinosinusitis in a pediatric population.

artículo científico publicado en 2014

Genetically Determined Birthweight Associates with Atrial Fibrillation: A Mendelian Randomization Study

scientific article published on 27 April 2020

Genetics of Bone Mass in Childhood and Adolescence: Effects of Sex and Maturation Interactions

artículo científico publicado en 2015

Genetics of childhood obesity

artículo científico publicado en 2011

Genetics of obesity and type 2 diabetes in African Americans.

artículo científico publicado en 2013

Genetics of pediatric bone strength

artículo científico publicado en 2016

Genome-scale Capture C promoter interactions implicate effector genes at GWAS loci for bone mineral density

article

Genome-wide analyses of ChIP-Seq derived FOXA2 DNA occupancy in liver points to genetic networks underpinning multiple complex traits.

artículo científico publicado en 2014

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

artículo científico publicado en 2009

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

artículo científico publicado en 2015

Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity

artículo científico publicado en 2013

Genome-wide association of body fat distribution in African ancestry populations suggests new loci

artículo científico publicado en 2013

Genome-wide association studies (GWAS): impact on elucidating the aetiology of diabetes.

scientific article published on October 2011

Genome-wide association studies in type 1 diabetes, inflammatory bowel disease and other immune-mediated disorders.

artículo científico publicado en 2009

Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.

artículo científico publicado en 2011

Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).

artículo científico publicado en 2011

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

artículo científico publicado en 2016

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

artículo científico publicado en 2011

Genotype and Tissue-Specific Effects on Alternative Splicing of the Transcription Factor 7-Like 2 Gene in Humans.

artículo científico publicado en 2010

Genotype and tissue-specific effects on alternative splicing of the transcription factor 7-like 2 gene in humans

artículo científico publicado en 2010

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

artículo científico publicado en 2009

IL-1 Transcriptional Responses to Lipopolysaccharides Are Regulated by a Complex of RNA Binding Proteins

artículo científico publicado en 2020

Identical osteochondritis dissecans lesions of the knee in sets of monozygotic twins.

artículo científico publicado en 2013

Identification of Genetic and Environmental Factors Predicting Metabolically Healthy Obesity in Children: Data From the BCAMS Study

artículo científico publicado en 2016

Impact of Common Diabetes Risk Variant in MTNR1B on Sleep, Circadian, and Melatonin Physiology.

artículo científico publicado en 2016

Implicating candidate genes at GWAS signals by leveraging topologically associating domains.

artículo científico

In silico replication of the genome-wide association results of the Type 1 Diabetes Genetics Consortium.

artículo científico publicado en 2010

Infant BMI or Weight-for-Length and Obesity Risk in Early Childhood.

artículo científico publicado en 2016

Influence of SNP*SNP interaction on BMI in European American adolescents: findings from the National Longitudinal Study of Adolescent Health

artículo científico publicado en 2015

Integrative genomics identifies LMO1 as a neuroblastoma oncogene

artículo científico publicado en 2010

Investigation of the locus near MC4R with childhood obesity in Americans of European and African ancestry

artículo científico publicado en 2009

Lack of relationship between mitochondrial heteroplasmy or variation and childhood obesity.

artículo científico publicado en 2011

Large copy-number variations are enriched in cases with moderate to extreme obesity.

artículo científico publicado en 2010

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

artículo científico publicado en 2012

Leveraging epigenomics and contactomics data to investigate SNP pairs in GWAS

artículo científico publicado en 2018

Leveraging genetic discoveries for sleep to determine causal relationships with common complex traits

artículo científico publicado en 2022

Leveraging putative enhancer-promoter interactions to investigate two-way epistasis in Type 2 Diabetes GWAS.

artículo científico publicado en 2018

Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects

artículo científico publicado en 2018

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

artículo científico publicado en 2008

Long PCR detection of the C4A null allele in B8-C4AQ0-C4B1-DR3

scientific article published on 01 October 2000

Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis

artículo científico publicado en 2017

Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis

scientific article published on 01 December 2018

Mapping effector genes at lupus GWAS loci using promoter Capture-C in follicular helper T cells

artículo científico publicado en 2020

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

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

artículo científico publicado en 2019

Mendelian randomization in the era of genomewide association studies.

artículo científico publicado en 2010

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

artículo científico publicado en 2010

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

artículo científico publicado en 2015

Microarray technology and applications in the arena of genome-wide association.

artículo científico publicado en 2008

Modeling genetic inheritance of copy number variations.

artículo científico publicado en 2008

Multi-dimensional bone density phenotyping reveals new insights in to genetic regulation of the pediatric skeleton

artículo científico publicado en 2017

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

artículo científico publicado en 2012

Next steps in the identification of gene targets for type 1 diabetes

artículo científico publicado en 2020

Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits

artículo científico publicado en 2020

ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry.

artículo científico publicado en 2008

Obesity-susceptibility loci and the tails of the pediatric BMI distribution.

artículo científico publicado en 2013

Overlap of genetic susceptibility to type 1 diabetes, type 2 diabetes, and latent autoimmune diabetes in adults.

artículo científico

PARP-1 Inhibition Rescues Short Lifespan in Hyperglycemic C. Elegans And Improves GLP-1 Secretion in Human Cells.

artículo científico publicado en 2018

Pathway-Based Genome-Wide Association Studies for Plasma Triglycerides in Obese Females and Normal-Weight Controls

artículo científico publicado en 2015

Pathway-Based Genome-wide Association Studies Reveal That the Rac1 Pathway Is Associated with Plasma Adiponectin Levels.

artículo científico publicado en 2015

Pathway-Wide Association Study Implicates Multiple Sterol Transport and Metabolism Genes in HDL Cholesterol Regulation.

artículo científico publicado en 2011

Pharmacogenetics and pharmacogenomics: tailored drug therapy for the 21st century

artículo científico publicado en 2001

Physical Activity Benefits the Skeleton of Children Genetically Predisposed to Lower Bone Density in Adulthood

artículo científico publicado en 2016

Physical activity and physical fitness: standardizing assessment with the PhenX Toolkit

artículo científico publicado en 2012

Polymorphisms of the interleukin-6 gene are associated with bone mineral density

artículo científico publicado en 1997

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2017

Public resources aid diabetes gene discovery

article

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2019

Rare EN1 Variants and Pediatric Bone Mass

artículo científico publicado en 2016

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

scientific article published on 14 January 2020

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

artículo científico publicado en 2010

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.

artículo científico publicado en 2010

Re: Ward K, Ogilvie JW, Singleton, et al. Validation of DNA-based prognostic testing to predict spinal curve progression in adolescent idiopathic scoliosis. Spine 2010;35:E1455-64

scientific article published on 01 July 2011

Recent development in pharmacogenomics: from candidate genes to genome-wide association studies.

artículo científico publicado en 2007

Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution

article

Relation of alleles of the collagen type Ialpha1 gene to bone density and the risk of osteoporotic fractures in postmenopausal women

artículo científico publicado en 1998

Relative Skeletal Maturation and Population Ancestry in Nonobese Children and Adolescents.

artículo científico publicado en 2016

Relevance of polymorphisms in MC4R and BDNF in short normal stature

scientific article published on 22 August 2018

Remapping the type I diabetes association of the CTLA4 locus

artículo científico publicado en 2009

Response to Comment on Schwartz et al. The Time Is Right for a New Classification System for Diabetes: Rationale and Implications of the β-Cell-Centric Classification Schema. Diabetes Care 2016;39:179-186.

artículo científico publicado en 2016

Restriction enzyme selection dictates detection range sensitivity in chromatin conformation capture-based variant-to-gene mapping approaches

artículo científico publicado en 2021

Role of BMI‐Associated Loci Identified in GWAS Meta‐Analyses in the Context of Common Childhood Obesity in European Americans ⬇️

artículo científico publicado el 21 de julio de 2011

SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variation

scientific article published on March 2009

Sleep Duration and Cardiometabolic Risk Among Chinese School-aged Children: Do Adipokines Play a Mediating Role?

artículo científico publicado en 2017

Sleep duration does not mediate or modify association of common genetic variants with type 2 diabetes

artículo científico publicado en 2013

Strategies for Genetic Studies of Complex Diseases ⬇️

artículo científico publicado el 6 de agosto de 2010

Strong synaptic transmission impact by copy number variations in schizophrenia

artículo científico publicado en 2010

Teasing Diabetes Apart, One Locus at a Time

artículo científico publicado en 2018

The Dynamic Origins of Type 1 Diabetes

scientific article published on 01 December 2018

The Genetics of Pediatric Obesity.

artículo científico publicado en 2015

The TCF7L2 Locus: A Genetic Window Into the Pathogenesis of Type 1 and Type 2 Diabetes

artículo científico publicado en 2019

The Time Is Right for a New Classification System for Diabetes: Rationale and Implications of the β-Cell-Centric Classification Schema.

artículo científico publicado en 2016

The genetics of human obesity

article

The inheritance of rheumatoid arthritis in Iceland ⬇️

artículo científico publicado el 1 de octubre de 2001

The missense variation landscape of FTO, MC4R, and TMEM18 in obese children of African Ancestry.

artículo científico publicado en 2013

The relationship between selected physiological variables of rowers and rowing performance as determined by a 2000 m ergometer test.

artículo científico publicado en 1999

The role of established East Asian obesity-related loci on pediatric leptin levels highlights a neuronal influence on body weight regulation in Chinese children and adolescents: the BCAMS study

artículo científico publicado en 2017

The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature

artículo científico publicado en 2010

The role of obesity-associated loci identified in genome-wide association studies in the determination of pediatric BMI

artículo científico publicado en 2009

The type 2 diabetes associated rs7903146 T allele within TCF7L2 is significantly under-represented in Hereditary Multiple Exostoses: insights into pathogenesis

artículo científico publicado en 2014

The type 2 diabetes presumed causal variant within TCF7L2 resides in an element that controls the expression of ACSL5.

artículo científico publicado en 2016

The type I diabetes association of the IL2RA locus.

artículo científico publicado en 2009

Trans-ethnic Evaluation Identifies Novel Low Frequency Loci Associated with 25-Hydroxyvitamin D Concentrations.

artículo científico publicado en 2018

Transcriptome profiling of human ulcerative colitis mucosa reveals altered expression of pathways enriched in genetic susceptibility loci

artículo científico publicado en 2014

Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study

artículo científico publicado en 2012

Two novel type 2 diabetes loci revealed through integration of TCF7L2 DNA occupancy and SNP association data

artículo científico publicado en 2014

Understanding the elusive mechanism of action of TCF7L2 in metabolism.

artículo científico publicado en 2012

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

artículo científico publicado en 2006

Variant-to-gene-mapping analyses reveal a role for pancreatic islet cells in conferring genetic susceptibility to sleep-related traits

artículo científico publicado en 2022

Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight

artículo científico publicado en 2010

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

article

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

artículo científico publicado en 2019

Variants of DENND1B associated with asthma in children

artículo científico publicado en 2009

Vitamin D receptor polymorphism, bone mineral density, and osteoporotic vertebral fracture: studies in a UK population.

artículo científico publicado en 1996

What's New in Osteoporosis? ⬇️

artículo científico publicado el 1 de febrero de 1995

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