Introducing COCOS: codon consequence scanner for annotating reading frame changes induced by stop-lost and frame shift variants

por Butkiewicz, Mariusz, Haines, Jonathan L, Bush, William S
Publicado 2017

Dissecting trait heterogeneity: a comparison of three clustering methods applied to genotypic data

por Thornton-Wells, Tricia A, Moore, Jason H, Haines, Jonathan L
Publicado 2006

The Impact of the Human Genome Project on Complex Disease

por Cooke Bailey, Jessica N., Pericak-Vance, Margaret A., Haines, Jonathan L.
Publicado 2014

DRUG-DRUG INTERACTION PROFILES OF MEDICATION REGIMENS EXTRACTED FROM A DE-IDENTIFIED ELECTRONIC MEDICAL RECORDS SYSTEM

por Butkiewicz, Mariusz, Restrepo, Nicole A., Haines, Jonathan L., Crawford, Dana C.
Publicado 2016

The GABBR1 locus and the G1465A variant is not associated with temporal lobe epilepsy preceded by febrile seizures

por Ma, Shaochun, Abou-Khalil, Bassel, Sutcliffe, James S, Haines, Jonathan L, Hedera, Peter
Publicado 2005

Automated extraction of clinical traits of multiple sclerosis in electronic medical records

por Davis, Mary F, Sriram, Subramaniam, Bush, William S, Denny, Joshua C, Haines, Jonathan L
Publicado 2013

Extracting Primary Open-Angle Glaucoma from Electronic Medical Records for Genetic Association Studies

por Restrepo, Nicole A., Farber-Eger, Eric, Goodloe, Robert, Haines, Jonathan L., Crawford, Dana C.
Publicado 2015

Enabling Genomic-Phenomic Association Discovery without Sacrificing Anonymity

por Heatherly, Raymond D., Loukides, Grigorios, Denny, Joshua C., Haines, Jonathan L., Roden, Dan M., Malin, Bradley A.
Publicado 2013

Correction: Enabling Genomic-Phenomic Association Discovery without Sacrificing Anonymity

por Heatherly, Raymond D., Loukides, Grigorios, Denny, Joshua C., Haines, Jonathan L., Roden, Dan M., Malin, Bradley A.
Publicado 2013

Pathway Analysis Integrating Genome-Wide and Functional Data Identifies PLCG2 as a Candidate Gene for Age-Related Macular Degeneration

por Waksmunski, Andrea R., Grunin, Michelle, Kinzy, Tyler G., Igo, Robert P., Haines, Jonathan L., Cooke Bailey, Jessica N.
Publicado 2019

Statistical driver genes as a means to uncover missing heritability for age-related macular degeneration

por Waksmunski, Andrea R., Grunin, Michelle, Kinzy, Tyler G., Igo, Robert P., Haines, Jonathan L., Cooke Bailey, Jessica N.
Publicado 2020

Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes

por Hutcheson, Holli B, Olson, Lana M, Bradford, Yuki, Folstein, Susan E, Santangelo, Susan L, Sutcliffe, James S, Haines, Jonathan L
Publicado 2004

Lack of association of polymorphisms in homocysteine metabolism genes with pseudoexfoliation syndrome and glaucoma

por Fan, Bao Jian, Chen, Teresa, Grosskreutz, Cynthia, Pasquale, Louis, Rhee, Douglas, DelBono, Elizabeth, Haines, Jonathan L., Wiggs, Janey L.
Publicado 2008

The Application of Genetic Risk Scores in Age-Related Macular Degeneration: A Review

por Cooke Bailey, Jessica N., Hoffman, Joshua D., Sardell, Rebecca J., Scott, William K., Pericak-Vance, Margaret A., Haines, Jonathan L.
Publicado 2016

FE65 Binds Teashirt, Inhibiting Expression of the Primate-Specific Caspase-4

por Kajiwara, Yuji, Akram, Afia, Katsel, Pavel, Haroutunian, Vahram, Schmeidler, James, Beecham, Gary, Haines, Jonathan L., Pericak-Vance, Margaret A., Buxbaum, Joseph D.
Publicado 2009

Mapping of the Disease Locus and Identification of ADAMTS10 As a Candidate Gene in a Canine Model of Primary Open Angle Glaucoma

por Kuchtey, John, Olson, Lana M., Rinkoski, Tommy, MacKay, Edward O., Iverson, T. M., Gelatt, Kirk N., Haines, Jonathan L., Kuchtey, Rachel W.
Publicado 2011

Hadoop and PySpark for reproducibility and scalability of genomic sequencing studies

por WHEELER, NICHOLAS R., BENCHEK, PENELOPE, KUNKLE, BRIAN W., HAMILTON-NELSON, KARA L., WARFE, MIKE, FONDRAN, JEREMY R., HAINES, JONATHAN L., BUSH, WILLIAM S.
Publicado 2020

A comparative analysis of the information content in long and short SAGE libraries

por Li, Yi-Ju, Xu, Puting, Qin, Xuejun, Schmechel, Donald E, Hulette, Christine M, Haines, Jonathan L, Pericak-Vance, Margaret A, Gilbert, John R
Publicado 2006

Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

por McCauley, Jacob L, Li, Chun, Jiang, Lan, Olson, Lana M, Crockett, Genea, Gainer, Kimberly, Folstein, Susan E, Haines, Jonathan L, Sutcliffe, James S
Publicado 2005

One for all and all for One: Improving replication of genetic studies through network diffusion

por Lancour, Daniel, Naj, Adam, Mayeux, Richard, Haines, Jonathan L., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Crovella, Mark, Farrer, Lindsay A., Kasif, Simon
Publicado 2018