C. Justice

发表

Rare copy number variants in males and females with childhood attention-deficit/hyperactivity disorder

P. Shaw, K. Ahn, G. Sudre, 2022, Molecular Psychiatry.

Intra-Familial Tests of Association between Familial Idiopathic Scoliosis and Linked Regions on 9q31.3–q34.3 and 16p12.3–q22.2

Alexander F. Wilson, A. F. Wilson, K. Doheny, 2012, Human Heredity.

Gain-of-function variants and overexpression of RUNX2 in patients with nonsyndromic midline craniosynostosis.

M. Barba, W. Lattanzi, H. Drissi, 2020, Bone.

A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9

Alexander F. Wilson, A. F. Wilson, J. Richtsmeier, 2012, Nature Genetics.

A genome wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP 2 and within BBS 9

Alexander F. Wilson, A. F. Wilson, J. Richtsmeier, 2012 .

A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21

Alexander F. Wilson, A. F. Wilson, E. Jabs, 2003, Human Genetics.

Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data

Alexander F. Wilson, A. F. Wilson, Claire L. Simpson, 2011, BMC proceedings.

Targeted Sequencing of Candidate Regions Associated with Sagittal and Metopic Nonsyndromic Craniosynostosis

Alexander F. Wilson, A. F. Wilson, R. Kaneva, 2022, Genes.

A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis

Jeremy A. Sabourin, Alexander F. Wilson, A. F. Wilson, 2020, Human Genetics.

Phylogenetic Analysis of the Friedreich Ataxia GAA Trinucleotide Repeat

M. Stoneking, M. Batzer, B. Keats, 2001, Journal of Molecular Evolution.

Sequencing of the TBX6 Gene in Families With Familial Idiopathic Scoliosis

O. Pourquié, A. Perera, Olivier Tassy, 2015, Spine deformity.

Phenotypic variability in friedreich ataxia: Role of the associated GAA triplet repeat expansion

F. Andermann, J. Bouchard, S. di Donato, 1997, Annals of neurology.

Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape

Ryan J. Eller, D. Vandermeulen, M. Shriver, 2022, bioRxiv.

Identification of Candidate Regions for Familial Idiopathic Scoliosis

Alexander F. Wilson, A. F. Wilson, K. Doheny, 2005, Spine.

Idiopathic Scoliosis: Identification of Candidate Regions on Chromosome 19p13

Alexander F. Wilson, A. F. Wilson, N. Miller, 2006, Spine.

Familial Idiopathic Scoliosis: Evidence of an X-Linked Susceptibility Locus

Alexander F. Wilson, A. F. Wilson, N. Miller, 2003, Spine.

Linkage analysis of genetic loci for kyphoscoliosis on chromosomes 5p13, 13q13.3, and 13q32

Alexander F. Wilson, A. F. Wilson, K. Doheny, 2006, American journal of medical genetics. Part A.

Comparison of year-of-exam- and age-matched estimates of heritability in the Framingham Heart Study data

Alexander F. Wilson, A. F. Wilson, E. Pugh, 2003, BMC Genetics.

CHD7 Gene Polymorphisms and Familial Idiopathic Scoliosis

Alexander F. Wilson, A. F. Wilson, N. Miller, 2013, Spine.

A variant associated with sagittal nonsyndromic craniosynostosis alters the regulatory function of a non‐coding element

A. F. Wilson, R. Sood, Jinoh Kim, 2017, American journal of medical genetics. Part A.

Evaluation of IRX Genes and Conserved Noncoding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis

Alexander F. Wilson, A. F. Wilson, J. Mullikin, 2016, G3: Genes, Genomes, Genetics.

Identification of susceptibility loci for scoliosis in FIS families with triple curves

Alexander F. Wilson, A. F. Wilson, A. Zorn, 2010, American journal of medical genetics. Part A.

Males With Familial Idiopathic Scoliosis: A Distinct Phenotypic Subgroup

N. Miller, C. M. Justice, M. Clough, 2010, Spine.

Lack of Association Between the Aggrecan Gene and Familial Idiopathic Scoliosis

Alexander F. Wilson, A. F. Wilson, N. Miller, 2006, Spine.

Comparison of Variance Components, ANOVA and Regression of Offspring on Midparent (ROMP) Methods for SNP Markers

Alexander F. Wilson, A. F. Wilson, E. Pugh, 2001, Genetic epidemiology.

Critical values and variation in type I error along chromosomes in the COGA dataset using the applied pseudo-trait method

A. F. Wilson, G. Papanicolaou, A. J. Sorant, 2005, BMC Genetics.

TBX3 and EFNA4 Variant in a Family with Ulnar-Mammary Syndrome and Sagittal Craniosynostosis

B. Darbro, P. Romitti, Anthony M. Musolf, 2022, Genes.

Type I error rates of rare single nucleotide variants are inflated in tests of association with non–normally distributed traits using simple linear regression methods

Jeremy A. Sabourin, A. F. Wilson, Tae‐Hwi Schwantes‐An, 2016, BMC Proceedings.

ADHD and its neurocognitive substrates: A two sample Mendelian randomization study

P. Shaw, K. Ahn, L. Norman, 2022, Translational Psychiatry.

Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428

R. Kaneva, T. Roscioli, M. Zwienenberg, 2024, Scientific reports.

Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits

J. Richtsmeier, E. Jabs, D. Staffenberg, 2024, Genetics in medicine open.