| Year |
Citation |
Score |
| 2020 |
Li YR, Glessner JT, Coe BP, Li J, Mohebnasab M, Chang X, Connolly J, Kao C, Wei Z, Bradfield J, Kim C, Hou C, Khan M, Mentch F, Qiu H, ... ... Hadley D, et al. Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations. Nature Communications. 11: 255. PMID 31937769 DOI: 10.1038/S41467-019-13624-1 |
0.374 |
|
| 2019 |
Khorfan K, Aljabban J, Gurakar M, Khan H, Aljabban N, Mukhtar M, Hadley D. 682 Investigating the Pathogenesis of Ulcerative Colitis Through Meta-Analysis of Gene Expression Omnibus Data The American Journal of Gastroenterology. 114. DOI: 10.14309/01.Ajg.0000592264.60606.11 |
0.323 |
|
| 2019 |
Aljabban J, Chen D, Cottini F, Syed S, Aljabban N, Syed S, Hughes T, Feldman D, Hadley D, Benson DM. Characterization of Monoclonal Gammopathy of Undetermined Significance Progression to Multiple Myeloma through Meta-Analysis of GEO Data Blood. 134: 4395-4395. DOI: 10.1182/Blood-2019-129699 |
0.341 |
|
| 2018 |
Kido T, Sikora-Wohlfeld W, Kawashima M, Kikuchi S, Kamatani N, Patwardhan A, Chen R, Sirota M, Kodama K, Hadley D, Butte AJ. Are minor alleles more likely to be risk alleles? Bmc Medical Genomics. 11: 3. PMID 29351777 DOI: 10.1186/S12920-018-0322-5 |
0.321 |
|
| 2018 |
Rappoport N, Toung J, Hadley D, Wong RJ, Fujioka K, Reuter J, Abbott CW, Oh S, Hu D, Eng C, Huntsman S, Bodian DL, Niederhuber JE, Hong X, Zhang G, et al. A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth. Scientific Reports. 8: 226. PMID 29317701 DOI: 10.1038/S41598-017-18246-5 |
0.346 |
|
| 2017 |
Glessner JT, Li J, Wang D, March M, Lima L, Desai A, Hadley D, Kao C, Gur RE, Cohen N, Sleiman PMA, Li Q, Hakonarson H. Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders. Genome Medicine. 9: 106. PMID 29191242 DOI: 10.1186/S13073-017-0494-1 |
0.347 |
|
| 2017 |
Hadley D, Pan J, El-Sayed O, Aljabban J, Aljabban I, Azad TD, Hadied MO, Raza S, Rayikanti BA, Chen B, Paik H, Aran D, Spatz J, Himmelstein D, Panahiazar M, et al. Precision annotation of digital samples in NCBI's gene expression omnibus. Scientific Data. 4: 170125. PMID 28925997 DOI: 10.1038/Sdata.2017.125 |
0.323 |
|
| 2017 |
Hoffman JD, Graff RE, Emami NC, Tai CG, Passarelli MN, Hu D, Huntsman S, Hadley D, Leong L, Majumdar A, Zaitlen N, Ziv E, Witte JS. Cis-eQTL-based trans-ethnic meta-analysis reveals novel genes associated with breast cancer risk. Plos Genetics. 13: e1006690. PMID 28362817 DOI: 10.1371/Journal.Pgen.1006690 |
0.327 |
|
| 2015 |
Hadied MO, El-Sayed O, Zaidi B, Al-Jabban J, Raza S, Al-Jabban I, Pan J, Azad T, Hadley D. Novel Meta-Analyses of Microarray Data First Step Toward Malaria Disease Signature Development Open Forum Infectious Diseases. 2. DOI: 10.1093/Ofid/Ofv133.1161 |
0.334 |
|
| 2014 |
Hadley D, Wu ZL, Kao C, Kini A, Mohamed-Hadley A, Thomas K, Vazquez L, Qiu H, Mentch F, Pellegrino R, Kim C, Connolly J, Glessner J, Hakonarson H. The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism. Nature Communications. 5: 4074. PMID 24927284 DOI: 10.1038/Ncomms5074 |
0.337 |
|
| 2014 |
Matsunami N, Hensel CH, Baird L, Stevens J, Otterud B, Leppert T, Varvil T, Hadley D, Glessner JT, Pellegrino R, Kim C, Thomas K, Wang F, Otieno FG, Ho K, et al. Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population. Molecular Autism. 5: 5. PMID 24467814 DOI: 10.1186/2040-2392-5-5 |
0.361 |
|
| 2013 |
Sleiman P, Wang D, Glessner J, Hadley D, Gur RE, Cohen N, Li Q, Hakonarson H. GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus. Scientific Reports. 3: 3075. PMID 24166486 DOI: 10.1038/Srep03075 |
0.329 |
|
| 2013 |
Matsunami N, Hadley D, Hensel CH, Christensen GB, Kim C, Frackelton E, Thomas K, da Silva RP, Stevens J, Baird L, Otterud B, Ho K, Varvil T, Leppert T, Lambert CG, et al. Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population. Plos One. 8: e52239. PMID 23341896 DOI: 10.1371/Journal.Pone.0052239 |
0.354 |
|
| 2012 |
Sanna-Cherchi S, Kiryluk K, Burgess KE, Bodria M, Sampson MG, Hadley D, Nees SN, Verbitsky M, Perry BJ, Sterken R, Lozanovski VJ, Materna-Kiryluk A, Barlassina C, Kini A, Corbani V, et al. Copy-number disorders are a common cause of congenital kidney malformations. American Journal of Human Genetics. 91: 987-97. PMID 23159250 DOI: 10.1016/J.Ajhg.2012.10.007 |
0.347 |
|
| 2012 |
Elia J, Glessner JT, Wang K, Takahashi N, Shtir CJ, Hadley D, Sleiman PM, Zhang H, Kim CE, Robison R, Lyon GJ, Flory JH, Bradfield JP, Imielinski M, Hou C, et al. Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. Nature Genetics. 44: 78-84. PMID 22138692 DOI: 10.1038/Ng.1013 |
0.356 |
|
| 2010 |
Chen W, Stambolian D, Edwards AO, Branham KE, Othman M, Jakobsdottir J, Tosakulwong N, Pericak-Vance MA, Campochiaro PA, Klein ML, Tan PL, Conley YP, Kanda A, Kopplin L, Li Y, ... ... Hadley D, et al. Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. Proceedings of the National Academy of Sciences of the United States of America. 107: 7401-6. PMID 20385819 DOI: 10.1073/Pnas.0912702107 |
0.33 |
|
| 2010 |
Hadley D, Orlin A, Brown G, Brucker AJ, Ho AC, Regillo CD, Donoso LA, Tian L, Kaderli B, Stambolian D. Analysis of six genetic risk factors highly associated with AMD in the region surrounding ARMS2 and HTRA1 on chromosome 10, region q26. Investigative Ophthalmology & Visual Science. 51: 2191-6. PMID 19933195 DOI: 10.1167/Iovs.09-3798 |
0.346 |
|
| 2009 |
Bucan M, Abrahams BS, Wang K, Glessner JT, Herman EI, Sonnenblick LI, Alvarez Retuerto AI, Imielinski M, Hadley D, Bradfield JP, Kim C, Gidaya NB, Lindquist I, Hutman T, Sigman M, et al. Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. Plos Genetics. 5: e1000536. PMID 19557195 DOI: 10.1371/Journal.Pgen.1000536 |
0.59 |
|
| 2006 |
Hadley D, Murphy T, Valladares O, Hannenhalli S, Ungar L, Kim J, Bućan M. Patterns of sequence conservation in presynaptic neural genes. Genome Biology. 7: R105. PMID 17096848 DOI: 10.1186/Gb-2006-7-11-R105 |
0.548 |
|
| Show low-probability matches. |