J. Bradfield

James T. Elder, H. Hakonarson, S. Grant, 2018, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

John A. Sweeney, Geraldine Dawson, Daniel H. Geschwind, 2009, PLoS genetics.

Genome-wide association study of the age of onset of type 1 diabetes reveals HTATIP2 as a novel T cell regulator

H. Hakonarson, C. Polychronakos, J. Bradfield, 2023, Frontiers in Immunology.

Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patients

John J. Connolly, Joseph T. Glessner, J. Glessner, 2021, Scientific Reports.

Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci

John J. Connolly, Joseph T. Glessner, J. Glessner, 2021, Communications biology.

Genetics of Low Polygenic Risk Score Type 1 Diabetes Patients: rare variants in 22 novel loci

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2020, medRxiv.

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

Robert T. Schultz, Takeshi Sakurai, Joseph Piven, 2009, Nature.

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

Susanne Walitza, Aribert Rothenberger, Takeshi Sakurai, 2011, Nature Genetics.

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

Tom R. Gaunt, Tom S. Price, Joseph T. Glessner, 2011, American journal of human genetics.

A Trans-ancestral Meta-Analysis of Genome-Wide Association Studies Reveals Loci Associated with Childhood Obesity.

Christopher D. Brown, A. Uitterlinden, M. McCarthy, 2019, Human molecular genetics.

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

Joseph T. Glessner, Hakon Hakonarson, J. Glessner, 2011, Obesity.

The Role of Obesity‐associated Loci Identified in Genome‐wide Association Studies in the Determination of Pediatric BMI

Joseph T. Glessner, Ryan M. Smith, J. Glessner, 2009, Obesity.

A Saturated Map of Common Genetic Variants Associated with Human Height from 5.4 Million Individuals of Diverse Ancestries

Aaron F. McDaid, Yan V. Sun, Cassandra N. Spracklen, 2022 .

The type I diabetes association of the IL2RA locus

C Polychronakos, H. Hakonarson, S. Grant, 2009, Genes and Immunity.

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

Joseph T. Glessner, Hakon Hakonarson, J. Glessner, 2009, The Journal of pediatrics.

A Genome-Wide Meta-Analysis of Six Type 1 Diabetes Cohorts Identifies Multiple Associated Loci

Constantin Polychronakos, Struan F. A. Grant, Joseph T. Glessner, 2011, PLoS genetics.

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

Samuel E. Jones, David M. Evans, K. Lunetta, 2017, bioRxiv.

Running Head: Genetic Correlations: Brain & Immune Phenotypes-1 1 Title: Genetic correlations among neuro-behavioral and immune-related phenotypes based on genome-

Annegret, James T. Elder, H. Hakonarson, 2017 .

Maternal genome-wide association study identifies a fasting glucose variant associated with offspring birth weight

Samuel E. Jones, David M. Evans, M. Jarvelin, 2015 .

Genetic studies of birth weight give biological insights into links with adult disease

Kyle J. Gaulton, Sara M. Willems, Samuel E. Jones, 2016 .

Imputation of TPMT defective alleles for the identification of patients with high-risk phenotypes

John J. Connolly, H. Hakonarson, J. Bradfield, 2014, Front. Genet..

Examination of genetic variants influencing lipid traits in pediatric populations

Joseph T. Glessner, Alexa J Moy, J. Glessner, 2012, Journal of Pediatric Genetics.

Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

Christian Gieger, Norman Delanty, Ellen Campbell, 2018, Nature Communications.

Genetic sharing and heritability of paediatric age of onset autoimmune diseases

Hongzhe Li, Constantin Polychronakos, Yiran Guo, 2015, Nature Communications.

Associations of autozygosity with a broad range of human phenotypes

May E. Montasser, Annelot M. Dekker, Blair H. Smith, 2019, Nature Communications.

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

Olli Simell, Mark I. McCarthy, Karen L. Mohlke, 2012, Nature Genetics.

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

Christopher D. Brown, Aaron F. McDaid, Yan V. Sun, 2021, bioRxiv.

Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy

H. Hakonarson, S. Grant, M. Sperling, 2021, Genes.

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

S. Grant, B. Voight, J. Bradfield, 2020, Nature Communications.

Association of HMGA2 Gene Variation with Height in Specific Pediatric Age Categories

Ryan M. Smith, J. Glessner, H. Hakonarson, 2008 .

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

Xiaowu Gai, Laura K Conlin, Livija Medne, 2009, Genome research.

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

Joseph T. Glessner, Ryan M. Smith, E. Zackai, 2009 .

ANGPT2 genetic variant is associated with trauma-associated acute lung injury and altered plasma angiopoietin-2 isoform ratio.

H. Hakonarson, Mingyao Li, R. Gallop, 2011, American journal of respiratory and critical care medicine.

Midazolam Dose Optimization in Critically Ill Pediatric Patients With Acute Respiratory Failure: A Population Pharmacokinetic-Pharmacogenomic Study

H. Hakonarson, J. Bradfield, A. Zuppa, 2019, Critical care medicine.

Morphine Dose Optimization in Critically Ill Pediatric Patients With Acute Respiratory Failure: A Population Pharmacokinetic-Pharmacogenomic Study

H. Hakonarson, J. Bradfield, A. Zuppa, 2019, Critical care medicine.

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

Hakon Hakonarson, Cuiping Hou, J. Glessner, 2010, American journal of human genetics.

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

J. Glessner, H. Hakonarson, Cecilia Kim, 2012, Obesity.

Investigation of the Locus Near MC4R With Childhood Obesity in Americans of European and African Ancestry

Joseph T. Glessner, Ryan M. Smith, J. Glessner, 2009, Obesity.

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

Hakon Hakonarson, J. Glessner, H. Hakonarson, 2008, Arthritis and rheumatism.

Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits - the Hispanic/Latino Anthropometry Consortium

H. Hakonarson, S. Grant, G. Bedoya, 2021, bioRxiv.

Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes

H. Hakonarson, A. Paterson, S. Grant, 2020, Diabetes.

Progress in Understanding Type 1 Diabetes Through Its Genetic Overlap with Other Autoimmune Diseases

H. Hakonarson, J. Bradfield, J. Roizen, 2015, Current Diabetes Reports.

Genome Wide Association Identifies PPFIA1 as a Candidate Gene for Acute Lung Injury Risk Following Major Trauma

H. Hakonarson, Cecilia Kim, Mingyao Li, 2012, PloS one.

Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche.

K. Lunetta, H. Hakonarson, S. Grant, 2021, Human reproduction.

Variants of DENND1B associated with asthma in children.

Ingo Ruczinski, James Flory, Terri H Beaty, 2010, The New England journal of medicine.

Whole-genome DNA/RNA sequencing identifies truncating mutations in RBCK1 in a novel Mendelian disease with neuromuscular and cardiac involvement

H. Hakonarson, Cecilia Kim, J. Bradfield, 2013, Genome Medicine.

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

Joseph T. Glessner, Hakon Hakonarson, Ryan M. Smith, 2008, Nature Genetics.

Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease.

Judy H. Cho, David T. Okou, Claire L. Simpson, 2017, Gastroenterology.

Crohn's disease and genetic hitchhiking at IBD5.

Chandler D. Gatenbee, H. Hakonarson, M. Bamshad, 2012, Molecular biology and evolution.

Crohn ’ s Disease and Genetic Hitchhiking at IBD 5

Chandler D. Gatenbee, H. Hakonarson, M. Bamshad, 2011 .

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

H. Hakonarson, Cecilia Kim, S. Grant, 2018, Diabetes Care.

Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

H. Hakonarson, Cecilia Kim, Yiran Guo, 2017, Scientific Reports.

A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

John J. Connolly, I. Ntalla, E. Zeggini, 2017, Scientific Reports.

BMD‐Associated Variation at the Osterix Locus Is Correlated With Childhood Obesity in Females

J. Glessner, H. Hakonarson, Cecilia Kim, 2011, Obesity.

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

David M. Evans, H. Hakonarson, X. Estivill, 2016, Human molecular genetics.

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

David M. Evans, H. Hakonarson, X. Estivill, 2016 .

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

Aad van der Lugt, Xavier Estivill, Sudha Seshadri, 2013, Nature Genetics.

Relative contribution of type 1 and type 2 diabetes loci to the genetic etiology of adult-onset, non-insulin-requiring autoimmune diabetes

H. Hakonarson, S. Grant, B. Voight, 2017, BMC Medicine.

GWAS-implicated in type 1 and type 2 diabetes loci: insight into their relative roles in the pathogenesis of Latent Autoimmune Diabetes in Adults (LADA)

H. Hakonarson, S. Grant, J. Bradfield, 2015 .

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

H. Hakonarson, S. Grant, J. Bradfield, 2015, Human molecular genetics.

Genome‐wide single nucleotide polymorphism‐based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa

H. Hakonarson, Cecilia Kim, J. Bradfield, 2019, Experimental dermatology.

Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.

Scott M. Williams, Yu-Han H. Hsu, Nicholette D. Palmer, 2021, American journal of human genetics.

Dominant Form of Congenital Hyperinsulinism Maps to HK1 Region on 10q

H. Hakonarson, J. Bradfield, C. Stanley, 2013, Hormone Research in Paediatrics.

Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder

Struan F. A. Grant, Joseph T. Glessner, Hakon Hakonarson, 2010, PloS one.

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

C Polychronakos, H. Hakonarson, S. Grant, 2009, Journal of Medical Genetics.

Using common genetic variants to find drugs for common epilepsies

David F. Smith, C. Gieger, I. Scheffer, 2021, Brain Communications.

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

Joseph T. Glessner, Ryan M. Smith, J. Glessner, 2007, Gut.

Remapping the type I diabetes association of the CTLA4 locus

C Polychronakos, H. Hakonarson, S. Grant, 2009, Genes and Immunity.

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

Ryan M. Smith, J. Glessner, Cecilia Kim, 2008, The Journal of allergy and clinical immunology.

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.

Joseph T. Glessner, Ryan M. Smith, J. Glessner, 2009, The Journal of allergy and clinical immunology.

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

H. Hakonarson, S. Grant, J. Bradfield, 2015, Bone.

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

H. Hakonarson, S. Grant, W. Pu, 2014, Molecular endocrinology.

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

H. Hakonarson, S. Grant, J. Bradfield, 2017, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

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

Joseph T. Glessner, Ryan M. Smith, J. Glessner, 2008, The application of clinical genetics.

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

Joseph T. Glessner, Bradley P. Coe, B. Coe, 2020, Nature Communications.

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

S. Grant, E. Lange, J. Bradfield, 2016, Pediatric obesity.

University of Southern Denmark Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC Mishra,

H. Hakonarson, L. Groop, K. Khunti, 2020 .

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

H. Hakonarson, S. Grant, L. Groop, 2019, Diabetes Care.

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

B. Coe, E. Eichler, J. Glessner, 2020, Nature Communications.

Understanding the genetic complexity of puberty timing across the allele frequency spectrum

M. P. Concas, M. Jarvelin, E. Demerath, 2023, medRxiv.

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

Marcelo P. Segura-Lepe, A. J. Slater, Dajiang J. Liu, 2018, Nature Genetics.

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

H. Hakonarson, Cecilia Kim, S. Grant, 2010, Human molecular genetics.

Germline Exome Sequencing for Men with Testicular Germ Cell Tumor Reveals Coding Defects in Chromosomal Segregation and Protein-targeting Genes.

H. Hakonarson, D. Rader, M. Greene, 2023, European urology.

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

Joseph T. Glessner, Ryan M. Smith, J. Glessner, 2007, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

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

Marcelo P. Segura-Lepe, A. J. Slater, Dajiang J. Liu, 2019, Nature Genetics.

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

J. Glessner, H. Hakonarson, Cecilia Kim, 2010, BMC Medical Genetics.

The ubiquitin ligase adaptor Ndfip1 regulates T cell-mediated gastrointestinal inflammation and inflammatory bowel disease susceptibility

H. Hakonarson, J. Bradfield, C. Riling, 2011, Mucosal Immunology.

Examination of All Type 2 Diabetes GWAS Loci Reveals HHEX-IDE as a Locus Influencing Pediatric BMI

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2009, Diabetes.

Examination of Type 2 Diabetes Loci Implicates CDKAL1 as a Birth Weight Gene

Joseph T. Glessner, Hakon Hakonarson, Patrick Sleiman, 2009, Diabetes.

Assessing the functional consequence of loss of function variants using electronic medical record and large-scale genomics consortium efforts

H. Hakonarson, J. Bradfield, F. Mentch, 2014, Front. Genet..

GWAS on longitudinal growth traits reveals different genetic factors influencing infant , child and adult 1 BMI 2 3

Frayling, P. O’Reilly, L. Coin, 2019 .

Associations of autozygosity with a broad range of human phenotypes

Peter K. Joshi, M. P. Concas, May E. Montasser, 2019, Nature Communications.

A saturated map of common genetic variants associated with human height

Aaron F. McDaid, M. P. Concas, Cassandra N. Spracklen, 2022, Nature.

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

I. Ntalla, D. Postma, D. Lawlor, 2012, Nature Genetics.

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

John J. Connolly, J. Glessner, H. Hakonarson, 2015, Nature Medicine.

Association Analysis of Type 2 Diabetes Loci in Type 1 Diabetes

Constantin Polychronakos, Hakon Hakonarson, Cecilia Kim, 2008, Diabetes.

Crohn's disease and genetic hitchhiking at IBD5.

Chandler D. Gatenbee, H. Hakonarson, M. Bamshad, 2012, Molecular biology and evolution.

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

Ethan M. Goldberg, Andreas M. Koupparis, W. C. Stewart, 2023, Nature Genetics.

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.

Christopher D. Brown, Aaron F. McDaid, M. P. Concas, 2022, American journal of human genetics.

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

T. Spector, D. Lawlor, H. Hakonarson, 2016, JAMA.

Implicating genes, pleiotropy and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

Anurag, Cassandra N. Spracklen, I. Ntalla, 2021, medRxiv.

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

J. Glessner, H. Hakonarson, Cecilia Kim, 2015, Nature Medicine.

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

John J. Connolly, J. Glessner, H. Hakonarson, 2015, Nature Medicine.

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

P. Elliott, M. Jarvelin, D. Postma, 2012, Nature Genetics.

The Role of Obesity‐associated Loci Identified in Genome‐wide Association Studies in the Determination of Pediatric BMI

Ryan M. Smith, J. Glessner, H. Hakonarson, 2009, Obesity.

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

Kyle J. Gaulton, Sara M. Willems, Samuel E. Jones, 2018, Nature Genetics.

Genetic correlations among psychiatric and immune-related Genetic correlations among psychiatric and immune-related phenotypes based on genome-wide association data [preprint] phenotypes based on genome-wide association data [preprint]

James T. Elder, H. Hakonarson, S. Grant, 2020 .

A Meta-Analysis Identifies New Loci Associated with Body Mass index in Individuals of African Ancestry

Gary K. Chen, Scott M. Williams, Nicholette D. Palmer, 2013, Nature Genetics.

Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3′ UTR of FAIM2

J. A. Maguire, S. Grant, J. Bradfield, 2024, Cell genomics.

Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits—The Hispanic/Latino Anthropometry Consortium

H. Hakonarson, S. Grant, G. Bedoya, 2022, HGG advances.

Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study

James T. Elder, T. Spector, H. Hakonarson, 2016, PLoS medicine.

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

Ryan M. Smith, J. Glessner, H. Hakonarson, 2008, The application of clinical genetics.

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

P. O’Reilly, P. Elliott, M. Jarvelin, 2010, Nature Genetics.

A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

John J. Connolly, I. Ntalla, E. Zeggini, 2017, Scientific Reports.

Analysis of shared heritability in common disorders of the brain

Janice M. Fullerton, Thomas W. Mühleisen, C. Sudlow, 2018, Science.

The Impact of Patterns in Linkage Disequilibrium and Sequencing Quality on the Imprint of Balancing Selection

J. Bradfield, Tychele N. Turner, Tristan J. Hayeck, 2024, Genome biology and evolution.

A framework for conducting time-varying genome-wide association studies: An application to body mass index across childhood in six multiethnic cohorts

H. Hakonarson, N. Warrington, J. Bradfield, 2024, medRxiv.

Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes

T. Lehtimäki, J. Glessner, H. Hakonarson, 2024, Genome biology.

Understanding the genetic complexity of puberty timing across the allele frequency spectrum

M. P. Concas, J. Murabito, S. Bandinelli, 2024, Nature genetics.