Author details

Full Name

Jonathan P Bradfield

Affiliation

ORCID

Career Start Year

2005

Papers

117

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37246069	Germline Exome Sequencing for Men with Testicular Germ Cell Tumor Reveals Coding Defects in Chromosomal Segregation and Protein-targeting Genes.	Eur Urol	2024
37503126	Understanding the genetic complexity of puberty timing across the allele frequency spectrum.	medRxiv	2023
36817429	Genome-wide association study of the age of onset of type 1 diabetes reveals HTATIP2 as a novel T cell regulator.	Front Immunol	2023
37012456	Genetic effects on the timing of parturition and links to fetal birth weight.	Nat Genet	2023
35347896	Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis.	Arthritis Rheumatol	2022
36268164	Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022
35399580	Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022
34362956	Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patients.	Sci Rep	2021
33950547	Combined application of genetic and polygenic risk scores for type 1 diabetes risk prediction.	Diabetes Obes Metab	2021
33713608	Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.	Am J Hum Genet	2021
34302048	Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci.	Commun Biol	2021
34021356	Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche.	Hum Reprod	2021
33157082	Association of DLL1 with type 1 diabetes in patients characterized by low polygenic risk score.	Metabolism	2021
34799566	Cis-regulatory architecture of human ESC-derived hypothalamic neuron differentiation aids in variant-to-gene mapping of relevant complex traits.	Nat Commun	2021
34573423	Genetic Variation in <i>PADI6-PADI4</i> on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy.	Genes (Basel)	2021
33045005	Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits.	PLoS Genet	2020
31843946	Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC.	Diabetes Care	2020
32005708	Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes.	Diabetes	2020
31937769	Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations.	Nat Commun	2020
32271392	Regulation of Janus Kinase 2 by an Inflammatory Bowel Disease Causal Non-coding Single Nucleotide Polymorphism.	J Crohns Colitis	2020
30672747	Midazolam Dose Optimization in Critically Ill Pediatric Patients With Acute Respiratory Failure: A Population Pharmacokinetic-Pharmacogenomic Study.	Crit Care Med	2019
31840077	GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI.	Sci Adv	2019
29364557	Genome-wide single nucleotide polymorphism-based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa.	Exp Dermatol	2019
30920410	Morphine Dose Optimization in Critically Ill Pediatric Patients With Acute Respiratory Failure: A Population Pharmacokinetic-Pharmacogenomic Study.	Crit Care Med	2019
31160809	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2019
29273807	Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29930110	Analysis of shared heritability in common disorders of the brain.	Science	2018
30254083	First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes.	Diabetes Care	2018
30325587	Genetic correlations among psychiatric and immune-related phenotypes based on genome-wide association data.	Am J Med Genet B Neuropsychiatr Genet	2018
29309628	Genome-wide association study of offspring birth weight in 86â¿¿577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics.	Hum Mol Genet	2018
29549330	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29549329	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29325163	Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations.	J Clin Endocrinol Metab	2018
28181694	A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites.	J Bone Miner Res	2017
28430825	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.	PLoS Genet	2017
28630421	A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.	Sci Rep	2017
28438156	Relative contribution of type 1 and type 2 diabetes loci to the genetic etiology of adult-onset, non-insulin-requiring autoimmune diabetes.	BMC Med	2017
28827695	Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.	Sci Rep	2017
27693347	Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease.	Gastroenterology	2017
27680694	Genome-wide associations for birth weight and correlations with adult disease.	Nature	2016
25893265	Influence of SNP*SNP interaction on BMI in European American adolescents: findings from the National Longitudinal Study of Adolescent Health.	Pediatr Obes	2016
26978208	Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight.	JAMA	2016
27327646	Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study.	PLoS Med	2016
26604143	Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index.	Hum Mol Genet	2016
27559109	A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.	Hum Mol Genet	2016
27554823	Mendelian randomization analysis demonstrates that low vitamin D is unlikely causative for pediatric asthma.	J Allergy Clin Immunol	2016
26450413	Genetic sharing and heritability of paediatric age of onset autoimmune diseases.	Nat Commun	2015
25498973	The type 2 diabetes associated rs7903146 T allele within TCF7L2 is significantly under-represented in Hereditary Multiple Exostoses: insights into pathogenesis.	Bone	2015
25281659	A novel common variant in DCST2 is associated with length in early life and height in adulthood.	Hum Mol Genet	2015
26131930	Directional dominance on stature and cognition inÂ diverse human populations.	Nature	2015