What makes a good prediction? Feature importance and beginning to open the black box of machine learning in genetics

por Musolf, Anthony M., Holzinger, Emily R., Malley, James D., Bailey-Wilson, Joan E.
Publicado 2021

Genome-wide linkage search for cancer susceptibility loci in a cohort of non BRCA1/2 families in Sri Lanka

por Wijesiriwardhana, Prabhavi, Musolf, Anthony M., Bailey-Wilson, Joan E., Wetthasinghe, T. Kalum, Dissanayake, Vajira H. W.
Publicado 2022

Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p

por Musolf, Anthony M., Simpson, Claire L., Moiz, Bilal A., Long, Kyle A., Portas, Laura, Murgia, Federico, Ciner, Elise B., Stambolian, Dwight, Bailey-Wilson, Joan E.
Publicado 2017

Myopia in Chinese families shows linkage to 10q26.13

por Musolf, Anthony M., Simpson, Claire L., Long, Kyle A., Moiz, Bilal A., Lewis, Deyana D., Middlebrooks, Candace D., Portas, Laura, Murgia, Federico, Ciner, Elise B., Bailey-Wilson, Joan E., Stambolian, Dwight
Publicado 2018

Myopia in African Americans Is Significantly Linked to Chromosome 7p15.2-14.2

por Simpson, Claire L., Musolf, Anthony M., Cordero, Roberto Y., Cordero, Jennifer B., Portas, Laura, Murgia, Federico, Lewis, Deyana D., Middlebrooks, Candace D., Ciner, Elise B., Bailey-Wilson, Joan E., Stambolian, Dwight
Publicado 2021

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

por Justice, Cristina M., Musolf, Anthony M., Cuellar, Araceli, Lattanzi, Wanda, Simeonov, Emil, Kaneva, Radka, Paschall, Justin, Cunningham, Michael, Wilkie, Andrew O. M., Wilson, Alexander F., Romitti, Paul A., Boyadjiev, Simeon A.
Publicado 2022

Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia

por Guggenheim, Jeremy A, Clark, Rosie, Cui, Jiangtian, Terry, Louise, Patasova, Karina, Haarman, Annechien E G, Musolf, Anthony M, Verhoeven, Virginie J M, Klaver, Caroline C W, Bailey-Wilson, Joan E, Hysi, Pirro G, Williams, Cathy
Publicado 2022

Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families

por Simpson, Claire L., Musolf, Anthony M., Li, Qing, Portas, Laura, Murgia, Federico, Cordero, Roberto Y., Cordero, Jennifer B., Moiz, Bilal A., Holzinger, Emily R., Middlebrooks, Candace D., Lewis, Deyana D., Bailey-Wilson, Joan E., Stambolian, Dwight
Publicado 2019

Familial Lung Cancer: A Brief History from the Earliest Work to the Most Recent Studies

por Musolf, Anthony M., Simpson, Claire L., de Andrade, Mariza, Mandal, Diptasri, Gaba, Colette, Yang, Ping, Li, Yafang, You, Ming, Kupert, Elena Y., Anderson, Marshall W., Schwartz, Ann G., Pinney, Susan M., Amos, Christopher I., Bailey-Wilson, Joan E.
Publicado 2017

Association analyses of rare variants identify two genes associated with refractive error

por Patasova, Karina, Haarman, Annechien E. G., Musolf, Anthony M., Mahroo, Omar A., Rahi, Jugnoo S., Falchi, Mario, Verhoeven, Virginie J. M., Bailey-Wilson, Joan E., Klaver, Caroline C. W., Duggal, Priya, Klein, Alison, Guggenheim, Jeremy A., Hammond, Chris J., Hysi, Pirro G.
Publicado 2022

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

por Goovaerts, Seppe, Hoskens, Hanne, Eller, Ryan J., Herrick, Noah, Musolf, Anthony M., Justice, Cristina M., Yuan, Meng, Naqvi, Sahin, Lee, Myoung Keun, Vandermeulen, Dirk, Szabo-Rogers, Heather L., Romitti, Paul A., Boyadjiev, Simeon A., Marazita, Mary L., Shaffer, John R., Shriver, Mark D., Wysocka, Joanna, Walsh, Susan, Weinberg, Seth M., Claes, Peter
Publicado 2023

IMI 2021 Yearly Digest

por Jong, Monica, Jonas, Jost B., Wolffsohn, James S., Berntsen, David A., Cho, Pauline, Clarkson-Townsend, Danielle, Flitcroft, Daniel I., Gifford, Kate L., Haarman, Annechien E. G., Pardue, Machelle T., Richdale, Kathryn, Sankaridurg, Padmaja, Tedja, Milly S., Wildsoet, Christine F., Bailey-Wilson, Joan E., Guggenheim, Jeremy A., Hammond, Christopher J., Kaprio, Jaakko, MacGregor, Stuart, Mackey, David A., Musolf, Anthony M., Klaver, Caroline C. W., Verhoeven, Virginie J. M., Vitart, Veronique, Smith, Earl L.
Publicado 2021

Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

por Musolf, Anthony M., Haarman, Annechien E. G., Luben, Robert N., Ong, Jue-Sheng, Patasova, Karina, Trapero, Rolando Hernandez, Marsh, Joseph, Jain, Ishika, Jain, Riya, Wang, Paul Zhiping, Lewis, Deyana D., Tedja, Milly S., Iglesias, Adriana I., Li, Hengtong, Cowan, Cameron S., Biino, Ginevra, Klein, Alison P., Duggal, Priya, Mackey, David A., Hayward, Caroline, Haller, Toomas, Metspalu, Andres, Wedenoja, Juho, Pärssinen, Olavi, Cheng, Ching-Yu, Saw, Seang-Mei, Stambolian, Dwight, Hysi, Pirro G., Khawaja, Anthony P., Vitart, Veronique, Hammond, Christopher J., van Duijn, Cornelia M., Verhoeven, Virginie J. M., Klaver, Caroline C. W., Bailey-Wilson, Joan E.
Publicado 2023