List of works by Michael N Weedon

A Common Allele in FGF21 Associated with Sugar Intake Is Associated with Body Shape, Lower Total Body-Fat Percentage, and Higher Blood Pressure.

scientific article published in April 2018

A Large-Scale Association Analysis of Common Variation of the HNF1 Gene With Type 2 Diabetes in the U.K. Caucasian Population

article

A Type 1 Diabetes Genetic Risk Score Can Aid Discrimination Between Type 1 and Type 2 Diabetes in Young Adults

scientific article published on 17 November 2015

A Type 1 Diabetes Genetic Risk Score Can Identify Patients With GAD65 Autoantibody-Positive Type 2 Diabetes Who Rapidly Progress to Insulin Therapy

scientific article published on 23 October 2018

A Type 1 Diabetes Genetic Risk Score Predicts Progression of Islet Autoimmunity and Development of Type 1 Diabetes in Individuals at Risk

article

A cautionary tale: the non-causal association between type 2 diabetes risk SNP, rs7756992, and levels of non-coding RNA, CDKAL1-v1

scientific article

A central role for GRB10 in regulation of islet function in man.

scientific article published on 3 April 2014

A common allele in FGF21 associated with preference for sugar consumption lowers body fat in the lower body and increases blood pressure

scholarly article published 6 November 2017

A common genetic variant in the 15q24 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) is associated with a reduced ability of women to quit smoking in pregnancy

scientific article published on 09 May 2009

A common haplotype of the glucokinase gene alters fasting glucose and birth weight: association in six studies and population-genetics analyses

scientific article published on 6 October 2006

A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

scientific article

A common variant of HMGA2 is associated with adult and childhood height in the general population

scientific article

A common variant of the interleukin 6 receptor (IL-6r) gene increases IL-6r and IL-6 levels, without other inflammatory effects.

scientific article published on 02 August 2007

A common variation in deiodinase 1 gene DIO1 is associated with the relative levels of free thyroxine and triiodothyronine

scientific article published on 20 May 2008

A genome-wide association search for type 2 diabetes genes in African Americans

scientific article published on 4 January 2012

A genome-wide association study identifies protein quantitative trait loci (pQTLs)

scientific article

A genome-wide association study of early menopause and the combined impact of identified variants

scientific article published on 9 January 2013

A partially inactivating mutation in the sodium-dependent lysophosphatidylcholine transporter MFSD2A causes a non-lethal microcephaly syndrome

scientific article published on 25 May 2015

A role for coding functional variants in HNF4A in type 2 diabetes susceptibility

scientific article (publication date: 2011)

A single nucleotide polymorphism genetic risk score to aid diagnosis of coeliac disease: a pilot study in clinical care

scientific article published on 13 August 2020

A study of association between common variation in the growth hormone-chorionic somatomammotropin hormone gene cluster and adult fasting insulin in a UK Caucasian population

scientific article

Adherence to Oral Glucose-Lowering Therapies and Associations With 1-Year HbA1c: A Retrospective Cohort Analysis in a Large Primary Care Database.

scientific article published on 17 December 2015

Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data

scientific article

Adult height variants affect birth length and growth rate in children

scientific article

Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association

scientific article

An FTO variant is associated with Type 2 diabetes in South Asian populations after accounting for body mass index and waist circumference

scientific article

An in-frame deletion at the polymerase active site of POLD1 causes a multisystem disorder with lipodystrophy

scientific article

An interleukin-18 polymorphism is associated with reduced serum concentrations and better physical functioning in older people

scientific article published on January 2007

Analysis of large-scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemia.

scientific article

Another explanation for apparent epistasis

scientific article published in Nature

Assessing the Causal Role of Sleep Traits on Glycated Hemoglobin: A Mendelian Randomization Study

scientific article published in 2022

Assessing the combined impact of 18 common genetic variants of modest effect sizes on type 2 diabetes risk

scientific article published on 30 June 2008

Assessing the pathogenicity, penetrance and expressivity of putative disease-causing variants in a population setting

Assessment of MTNR1B Type 2 Diabetes Genetic Risk Modification by Shift Work and Morningness-Eveningness Preference in the UK Biobank

scientific article published on 22 November 2019

Assessment of the role of common genetic variation in the transient neonatal diabetes mellitus (TNDM) region in type 2 diabetes: a comparative genomic and tagging single nucleotide polymorphism approach

scientific article

Association Analysis of 6,736 U.K. Subjects Provides Replication and ConfirmsTCF7L2as a Type 2 Diabetes Susceptibility Gene With a Substantial Effect on Individual Risk

article

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

scientific article (publication date: November 2010)

Association analysis of 29,956 individuals confirms that a low-frequency variant at CCND2 halves the risk of type 2 diabetes by enhancing insulin secretion

scientific article published on 20 January 2015

Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses

article

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

scientific article

Beta cell glucose sensitivity is decreased by 39% in non-diabetic individuals carrying multiple diabetes-risk alleles compared with those with no risk alleles.

scientific article

Biological and clinical insights from genetics of insomnia symptoms

article

Biological and clinical insights from genetics of insomnia symptoms

scientific article published on 25 February 2019

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

scientific article published on 29 September 2017

Chapter 1 Transcription factor genes in type 2 diabetes

article

Clinical Features and HLA Association of 5-Aminosalicylate (5-ASA)-induced Nephrotoxicity in Inflammatory Bowel Disease.

scientific article published on 29 November 2015

Clinical and research uses of genetic risk scores in type 1 diabetes

article

Cohort profile for the MASTERMIND study: using the Clinical Practice Research Datalink (CPRD) to investigate stratification of response to treatment in patients with type 2 diabetes

scientific article

Combining information from common type 2 diabetes risk polymorphisms improves disease prediction

scientific article

Common Variants of the Hepatocyte Nuclear Factor-4 P2 Promoter Are Associated With Type 2 Diabetes in the U.K. Population

scientific article published on 01 November 2004

Common genetic variants are significant risk factors for early menopause: results from the Breakthrough Generations Study

scientific article

Common genetic variation in the gene encoding interleukin-1-receptor antagonist (IL-1RA) is associated with altered circulating IL-1RA levels

article

Common variants in WFS1 confer risk of type 2 diabetes

scientific article published on July 2007

Common variants near MC4R are associated with fat mass, weight and risk of obesity

scientific article

Common variants of the novel type 2 diabetes genes CDKAL1 and HHEX/IDE are associated with decreased pancreatic beta-cell function

scientific article

Common variants show predicted polygenic effects on height in the tails of the distribution, except in extremely short individuals

scientific article

Common variation in the FTO gene alters diabetes-related metabolic traits to the extent expected given its effect on BMI

scientific article

Common variations in the ALMS1 gene do not contribute to susceptibility to type 2 diabetes in a large white UK population.

scientific article published on 7 April 2006

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

scientific article published on 18 March 2012

Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution.

scientific article published on 27 July 2009

Corrigendum: Clinical Features and HLA Association of 5-Aminosalicylate (5-ASA)-induced Nephrotoxicity in Inflammatory Bowel Disease

scientific article published on 01 December 2017

Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

scholarly article published in Nature Genetics

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

scientific article

Disentangling the genetics of lean mass

article

Effects of the diabetes linked TCF7L2 polymorphism in a representative older population

scientific article

Epigenetic regulation of mitochondrial function in neurodegenerative disease: New insights from advances in genomic technologies

scientific article published on 10 February 2016

Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

scientific article

Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

scientific article published in November 2011

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

scientific article published in May 2010

Estimating sleep parameters using an accelerometer without sleep diary

article

Estimating sleep parameters using an accelerometer without sleep diary

scientific article published in Scientific Reports

Evaluation of Common Variants in the Six Known Maturity-Onset Diabetes of the Young (MODY) Genes for Association With Type 2 Diabetes

article

Events in Early Life are Associated with Female Reproductive Ageing: A UK Biobank Study

scientific article published on 20 April 2016

Evidence that low socioeconomic position accentuates genetic susceptibility to obesity

article published in 2016

Exome sequencing identifies a DYNC1H1 mutation in a large pedigree with dominant axonal Charcot-Marie-Tooth disease

scientific article

FTO gene variants are strongly associated with type 2 diabetes in South Asian Indians.

scientific article

Frequency and phenotype of type 1 diabetes in the first six decades of life: a cross-sectional, genetically stratified survival analysis from UK Biobank

scientific article published on 30 November 2017

Functional variation in VEGF is not associated with type 2 diabetes in a United Kingdom Caucasian population

scientific article published on 09 May 2006

GWAS identifies novel risk locus for erectile dysfunction and implicates hypothalamic neurobiology and diabetes in etiology

GWAS in 446,118 European adults identifies 78 genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates

article

Gene-obesogenic environment interactions in the UK Biobank study

scientific article published on 10 January 2017

Genetic Evidence for a Link Between Favorable Adiposity and Lower Risk of Type 2 Diabetes, Hypertension, and Heart Disease

scientific article published on 26 April 2016

Genetic Variation in the Small Heterodimer Partner Gene and Young-Onset Type 2 Diabetes, Obesity, and Birth Weight in U.K. Subjects

article

Genetic evidence of assortative mating in humans

article

Genetic evidence that lower circulating FSH levels lengthen menstrual cycle, increase age at menopause and impact female reproductive health

scientific article

Genetic evidence that lower circulating FSH levels lengthen menstrual cycle, increase age at menopause, and impact reproductive health: a UK Biobank study

article

Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes

scientific article published on 18 November 2009

Genetic regulation of birth weight and fasting glucose by a common polymorphism in the islet cell promoter of the glucokinase gene

scientific article published in February 2005

Genetic risk scores in adult-onset type 1 diabetes – Authors' reply

scientific article published on 01 March 2018

Genetic scores to stratify risk of developing multiple islet autoantibodies and type 1 diabetes: A prospective study in children.

scientific article published on 3 April 2018

Genetic studies of accelerometer-based sleep measures in 85,670 individuals yield new insights into human sleep behaviour

article published in 2018

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

scientific article

Genetic variants associated with glycine metabolism and their role in insulin sensitivity and type 2 diabetes

scientific article published on February 2013

Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

scientific journal article

Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci.

scientific article

Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci

scientific article published on 14 July 2016

Genome-Wide and Abdominal MRI-Imaging Data Provides Evidence that a Genetically Determined Favourable Adiposity Phenotype is Characterized by Lower Ectopic Liver Fat and Lower Risk of Type 2 Diabetes, Heart Disease and Hypertension

scientific article published on 23 October 2018

Genome-wide association analyses in >119,000 individuals identifies thirteen morningness and two sleep duration loci

Genome-wide association analyses of chronotype in 697,828 individuals provides new insights into circadian rhythms in humans and links to disease

Genome-wide association analysis of excessive daytime sleepiness identifies 42 loci that suggest phenotypic subgroups

Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes

scientific article published on 13 August 2019

Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

scientific article

Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution

scientific article published in June 2009

Genome-wide association studies of human growth traits

scientific article published on 22 January 2013

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

scientific article

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

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

Genomic inflation factors under polygenic inheritance

scientific article

HLA-DQA1-HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants.

scientific article published on 14 September 2014

HUMAN LONGEVITY IS INFLUENCED BY MANY GENETIC VARIANTS: EVIDENCE FROM 75,000 UK BIOBANK PARTICIPANTS

Height, body mass index, and socioeconomic status: mendelian randomisation study in UK Biobank

scientific article

Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance

scientific article published on 12 October 2017

Heterozygous RFX6 protein truncating variants cause Maturity-Onset Diabetes of the Young (MODY) with reduced penetrance

Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants

scientific article published on 23 March 2016

Hundreds of variants clustered in genomic loci and biological pathways affect human height

scientific article

Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene

scientific article published on 23 March 2015

Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene

scientific article published on 4 January 2016

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

scientific article published on 14 April 2013

Improved genetic testing for monogenic diabetes using targeted next-generation sequencing.

scientific article published on 15 June 2013

Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation

scientific article

Insights on pathogenesis of type 2 diabetes from MODY genetics

scientific article published on April 2007

Interactions between light and growing season temperatures on, growth and development and gas exchange of Semillon (Vitis vinifera L.) vines grown in an irrigated vineyard

article

Interrogating type 2 diabetes genome-wide association data using a biological pathway-based approach

scientific article

Investigating causal relations between sleep traits and risk of breast cancer in women: mendelian randomisation study

scientific article published on 26 June 2019

Investigating causal relationships between sleep traits and risk of breast cancer: a Mendelian randomization study

Is disrupted sleep a risk factor for Alzheimer's disease? Evidence from a two-sample Mendelian randomization analysis

scientific article published on 05 November 2020

Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

scientific article

Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes

scientific article published in February 2003

Length of FMR1 repeat alleles within the normal range does not substantially affect the risk of early menopause

scientific article published on 09 September 2016

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

scientific article published on 01 May 2019

Mendelian randomization studies do not support a role for raised circulating triglyceride levels influencing type 2 diabetes, glucose levels, or insulin resistance

scientific article

Meta-analysis and a large association study confirm a role for calpain-10 variation in type 2 diabetes susceptibility

scientific article published on November 2003

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

scientific article

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

scientific article

Meta-analysis of genome-wide association data identifies two loci influencing age at menarche

scientific article

Meta-analysis of genome-wide association studies for height and body mass index in ~700,000 individuals of European ancestry

scholarly article published 2 March 2018

Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry

article

Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes

scientific article published on 5 February 2018

Modelling photosynthetic responses to temperature of grapevine (Vitis vinifera cv. Semillon) leaves on vines grown in a hot climate

article

Mosaic Turner syndrome shows reduced penetrance in an adult population study

scientific article published on 05 September 2018

Mosaic Turner syndrome shows reduced phenotypic penetrance in an adult population study compared to clinically ascertained cases

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

scientific article

Next generation sequencing of chromosomal rearrangements in patients with split-hand/split-foot malformation provides evidence for DYNC1I1 exonic enhancers of DLX5/6 expression in humans

scientific article published on 23 January 2014

Next-generation sequencing reveals deep intronic cryptic ABCC8 and HADH splicing founder mutations causing hyperinsulinism by pseudoexon activation

scientific article

No Evidence of Association of ENPP1 Variants With Type 2 Diabetes or Obesity in a Study of 8,089 U.K. Caucasians

scientific article published on 01 November 2006

Novel homozygous missense mutation in GAN associated with Charcot-Marie-Tooth disease type 2 in a large consanguineous family from Israel

scientific article

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

scientific article

PLIN1 Haploinsufficiency Is Not Associated With Lipodystrophy

Phosphodiesterase 8B Gene Polymorphism Is Associated with Subclinical Hypothyroidism in Pregnancy

article

Pitfalls of haplotype phasing from amplicon-based long-read sequencing

scientific article

Pleiotropic Effects of Trait-Associated Genetic Variation on DNA Methylation: Utility for Refining GWAS Loci.

scientific article

Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2.

scientific article published on 3 April 2017

Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A diabetes

scientific article

Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies

scientific article published on 26 August 2008

Precision Medicine in Type 2 Diabetes: Clinical Markers of Insulin Resistance Are Associated With Altered Short- and Long-Term Glycemic Response to DPP-4 Inhibitor Therapy.

scientific article published on 31 January 2018

Predicting human height by Victorian and genomic methods

scientific article

Quantifying the extent to which index event biases influence large genetic association studies

scientific article published on 30 December 2016

Quantifying the extent to which index event biases influence large genetic association studies

article

Quantitative traits associated with the Type 2 diabetes susceptibility allele in Kir6.2

scientific article published on 18 June 2003

Reaching new heights: insights into the genetics of human stature

scientific article published on 22 October 2008

Recent Progress in Identifying Genes Contributing to Type 2 Diabetes and Metabolic Syndrome

article

Recent Progress in the Identification of Genes Predisposing to the Metabolic Syndrome

article

Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis.

scientific article

Red Blood Cell Distribution Width: genetic evidence for aging pathways in 116,666 volunteers

Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers.

scientific article published on 28 September 2017

Refinement of the critical genomic region for hypoglycaemia in the Chromosome 9p deletion syndrome

scientific article published on 08 October 2019

Regional differences in mitochondrial DNA methylation in human post-mortem brain tissue

scientific article

Relationship between E23K (an established type II diabetes-susceptibility variant within KCNJ11), polycystic ovary syndrome and androgen levels

article published in 2007

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

scientific article (publication date: June 2007)

Retrovirally expressed metal response element-binding transcription factor-1 normalizes metallothionein-1 gene expression and protects cells against zinc, but not cadmium, toxicity

scientific article

SavvyCNV: Genome-wide CNV calling from off-target reads

scientific article published on 16 March 2022

Sex and BMI Alter the Benefits and Risks of Sulfonylureas and Thiazolidinediones in Type 2 Diabetes: A Framework for Evaluating Stratification Using Routine Clinical and Individual Trial Data

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

scientific article

Socio-economic and clinical factors predictive of paediatric quality of life post burn

scientific article published on 19 January 2011

Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases

scientific article

Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity

scientific article

Tall stories: the fundamental difficulties of genetic association studies

scientific article published on 01 January 2004

Targeted Allelic Expression Profiling in Human Islets Identifiescis-Regulatory Effects for Multiple Variants Identified by Type 2 Diabetes Genome-Wide Association Studies

scientific article published on 12 November 2014

The Common Variant I27L Is a Modifier of Age at Diabetes Diagnosis in Individuals With HNF1A-MODY

scientific article published on 12 June 2018

The Common p.R114W HNF4A Mutation Causes a Distinct Clinical Subtype of Monogenic Diabetes

scientific article published on 02 August 2016

The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype

scientific article

The acute transcriptional response to resistance exercise: impact of age and contraction mode

The functional "KL-VS" variant of KLOTHO is not associated with type 2 diabetes in 5028 UK Caucasians

scientific article

The impact of high temperatures on Vitis vinifera cv. Semillon grapevine performance and berry ripening.

scientific article published on 03 December 2013

The importance of TCF7L2.

scientific article published on October 2007

The transcription factor 7-like 2 (TCF7L2) gene is associated with Type 2 diabetes in UK community-based cases, but the risk allele frequency is reduced compared with UK cases selected for genetic studies.

scientific article published on 24 August 2007

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

scientific article

Triglyceride associated polymorphisms of the APOA5 gene have very different allele frequencies in Pune, India compared to Europeans

scientific article

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

scientific article

Type 1 Diabetes Genetic Risk Score: A Novel Tool to Discriminate Monogenic and Type 1 Diabetes

scientific article published on 05 April 2016

Type 1 diabetes genetic risk score is discriminative of diabetes in non-Europeans: evidence from a study in India

scientific article published on 11 June 2020

Type 2 diabetes TCF7L2 risk genotypes alter birth weight: a study of 24,053 individuals

scientific article published on 23 April 2007

Type 2 diabetes risk alleles are associated with reduced size at birth

scientific article published on 19 February 2009

Using Genetic Variants to Assess the Relationship Between Circulating Lipids and Type 2 Diabetes

scientific article published on 6 May 2015

Using genetics to understand the causal influence of higher BMI on depression

article

Variants in the FTO and CDKAL1 loci have recessive effects on risk of obesity and type 2 diabetes respectively

Variants in the FTO and CDKAL1 loci have recessive effects on risk of obesity and type 2 diabetes, respectively

scientific article published on 10 March 2016

Variants in the aromatase gene and on the Y-chromosome are not associated with adult height or insulin resistance in a UK population

scientific article published in August 2003

Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes

scientific article

Zinc Transporter 8 Autoantibodies (ZnT8A) and a Type 1 Diabetes Genetic Risk Score Can Exclude Individuals With Type 1 Diabetes From Inappropriate Genetic Testing for Monogenic Diabetes

scientific article published on 08 November 2018

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