Publications by authors named "Anthony Musolf"

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Next generation sequencing analysis reveals complex genetic architecture of childhood-onset systemic lupus erythematosus.
Laura Lewandowski, Linda Hiraki, Christiaan Scott, Ana Barrera-Vargas, Jorge Romo Tena, Anthony M Musolf

Lupus Sci Med· June 2025

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Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428.
Anthony M Musolf, Cristina M Justice, Zeynep Erdogan-Yildirim, Seppe Goovaerts, Araceli Cuellar

Sci Rep· April 2024

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Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape.
Seppe Goovaerts, Hanne Hoskens, Ryan J Eller, Noah Herrick, Anthony M Musolf

Nat Commun· November 2023

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Transmission disequilibrium analysis of whole genome data in childhood-onset systemic lupus erythematosus.
Kathleen M Vazzana, Anthony M Musolf, Joan E Bailey-Wilson, Linda T Hiraki, Earl D Silverman

Genes Immun· August 2023

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A likely HOXC4 predisposition variant for Chiari malformations.
Douglas L Brockmeyer, Samuel H Cheshier, Jeff Stevens, Julio C Facelli, Kerry Rowe, Anthony Musolf

J Neurosurg· July 2023

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A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall-cell lung cancer.
Lisa A Cannon-Albright, Craig C Teerlink, Jeff Stevens, Julio C Facelli, Shamus R Carr, Anthony M Musolf

Int J Cancer· July 2023

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Rare variant analyses across multiethnic cohorts identify novel genes for refractive error.
Anthony M Musolf, Annechien E G Haarman, Robert N Luben, Jue-Sheng Ong, Karina Patasova

Commun Biol· January 2023

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What makes a good prediction? Feature importance and beginning to open the black box of machine learning in genetics.
Anthony M Musolf, Emily R Holzinger, James D Malley, Joan E Bailey-Wilson

Hum Genet· September 2022

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Association analyses of rare variants identify two genes associated with refractive error.
Karina Patasova, Annechien E G Haarman, Anthony M Musolf, Omar A Mahroo, Jugnoo S Rahi

PLoS One· September 2022

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and Variant in a Family with Ulnar-Mammary Syndrome and Sagittal Craniosynostosis.
Moon Ley Tung, Bharatendu Chandra, Jaclyn Kotlarek, Marcelo Melo, Elizabeth Phillippi, Anthony Musolf

Genes (Basel)· September 2022

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Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia.
Jeremy A Guggenheim, Rosie Clark, Jiangtian Cui, Louise Terry, Karina Patasova, Anthony M Musolf

Hum Mol Genet· June 2022

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Genome-wide linkage search for cancer susceptibility loci in a cohort of non BRCA1/2 families in Sri Lanka.
Prabhavi Wijesiriwardhana, Anthony M Musolf, Joan E Bailey-Wilson, T Kalum Wetthasinghe, Vajira H W Dissanayake

BMC Res Notes· June 2022

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Targeted Sequencing of Candidate Regions Associated with Sagittal and Metopic Nonsyndromic Craniosynostosis.
Cristina M Justice, Anthony M Musolf, Araceli Cuellar, Wanda Lattanzi, Emil Simeonov

Genes (Basel)· May 2022

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Myopia in African Americans Is Significantly Linked to Chromosome 7p15.2-14.2.
Claire L Simpson, Anthony M Musolf, Roberto Y Cordero, Jennifer B Cordero, Laura Portas

Invest Ophthalmol Vis Sci· July 2021

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Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer.
Anthony M Musolf, Claire L Simpson, Bilal A Moiz, Claudio W Pikielny, Candace D Middlebrooks

Cancer Res· June 2021

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IMI 2021 Yearly Digest.
Monica Jong, Jost B Jonas, James S Wolffsohn, David A Berntsen, Pauline Cho, Anthony M Musolf

Invest Ophthalmol Vis Sci· April 2021

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Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q.
Anthony M Musolf, Bilal A Moiz, Haiming Sun, Claudio W Pikielny, Yohan Bossé

Cancer Epidemiol Biomarkers Prev· February 2020

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Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencing.
Anthony M Musolf, Winson S C Ho, Kyle A Long, Zhengping Zhuang, Davis P Argersinger

Eur J Hum Genet· October 2019

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Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33.
Anthony M Musolf, Claire L Simpson, Theresa A Alexander, Laura Portas, Federico Murgia

Hum Genet· April 2019

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Linear mixed models for association analysis of quantitative traits with next-generation sequencing data.
Chi-Yang Chiu, Fang Yuan, Bing-Song Zhang, Ao Yuan, Xin Li, Anthony M Musolf

Genet Epidemiol· March 2019

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Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families.
Claire L Simpson, Anthony M Musolf, Qing Li, Laura Portas, Federico Murgia

BMC Med Genet· January 2019

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Myopia in Chinese families shows linkage to 10q26.13.
Anthony M Musolf, Claire L Simpson, Kyle A Long, Bilal A Moiz, Deyana D Lewis

Mol Vis· November 2018

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Parametric Linkage Analysis Identifies Five Novel Genome-Wide Significant Loci for Familial Lung Cancer.
Anthony M Musolf, Claire L Simpson, Mariza de Andrade, Diptasri Mandal, Colette Gaba

Hum Hered· August 2017

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Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p.
Anthony M Musolf, Claire L Simpson, Bilal A Moiz, Kyle A Long, Laura Portas

Invest Ophthalmol Vis Sci· July 2017

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Familial Lung Cancer: A Brief History from the Earliest Work to the Most Recent Studies.
Anthony M Musolf, Claire L Simpson, Mariza de Andrade, Diptasri Mandal, Colette Gaba

Genes (Basel)· January 2017

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