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Page 1
Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry.
Genetics of Glaucoma in People of African Descent (GGLAD) Consortium; Hauser MA, Allingham RR, Aung T, Van Der Heide CJ, Taylor KD, Rotter JI, Wang SJ, Bonnemaijer PWM, Williams SE, Abdullahi SM, Abu-Amero KK, Anderson MG, Akafo S, Alhassan MB, Asimadu I, Ayyagari R, Bakayoko S, Nyamsi PB, Bowden DW, Bromley WC, Budenz DL, Carmichael TR, Challa P, Chen YI, Chuka-Okosa CM, Cooke Bailey JN, Costa VP, Cruz DA, DuBiner H, Ervin JF, Feldman RM, Flamme-Wiese M, Gaasterland DE, Garnai SJ, Girkin CA, Guirou N, Guo X, Haines JL, Hammond CJ, Herndon L, Hoffmann TJ, Hulette CM, Hydara A, Igo RP Jr, Jorgenson E, Kabwe J, Kilangalanga NJ, Kizor-Akaraiwe N, Kuchtey RW, Lamari H, Li Z, Liebmann JM, Liu Y, Loos RJF, Melo MB, Moroi SE, Msosa JM, Mullins RF, Nadkarni G, Napo A, Ng MCY, Nunes HF, Obeng-Nyarkoh E, Okeke A, Okeke S, Olaniyi O, Olawoye O, Oliveira MB, Pasquale LR, Perez-Grossmann RA, Pericak-Vance MA, Qin X, Ramsay M, Resnikoff S, Richards JE, Schimiti RB, Sim KS, Sponsel WE, Svidnicki PV, Thiadens AAHJ, Uche NJ, van Duijn CM, de Vasconcellos JPC, Wiggs JL, Zangwill LM, Risch N, Milea D, Ashaye A, Klaver CCW, Weinreb RN, Ashley Koch AE, Fingert JH, Khor CC. Genetics of Glaucoma in People of African Descent (GGLAD) Consortium, et al. Among authors: ashley koch ae. JAMA. 2019 Nov 5;322(17):1682-1691. doi: 10.1001/jama.2019.16161. JAMA. 2019. PMID: 31688885 Free PMC article.
Genomic screen and follow-up analysis for autistic disorder.
Shao Y, Wolpert CM, Raiford KL, Menold MM, Donnelly SL, Ravan SA, Bass MP, McClain C, von Wendt L, Vance JM, Abramson RH, Wright HH, Ashley-Koch A, Gilbert JR, DeLong RG, Cuccaro ML, Pericak-Vance MA. Shao Y, et al. Am J Med Genet. 2002 Jan 8;114(1):99-105. doi: 10.1002/ajmg.10153. Am J Med Genet. 2002. PMID: 11840513
No association between the WNT2 gene and autistic disorder.
McCoy PA, Shao Y, Wolpert CM, Donnelly SL, Ashley-Koch A, Abel HL, Ravan SA, Abramson RK, Wright HH, DeLong GR, Cuccaro ML, Gilbert JR, Pericak-Vance MA. McCoy PA, et al. Am J Med Genet. 2002 Jan 8;114(1):106-9. doi: 10.1002/ajmg.10182. Am J Med Genet. 2002. PMID: 11840514
Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes.
Rabionet R, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Rabionet R, et al. Among authors: ashley koch ae. Neurosci Lett. 2004 Dec 6;372(3):209-14. doi: 10.1016/j.neulet.2004.09.037. Neurosci Lett. 2004. PMID: 15542242
Analysis of the RELN gene as a genetic risk factor for autism.
Skaar DA, Shao Y, Haines JL, Stenger JE, Jaworski J, Martin ER, DeLong GR, Moore JH, McCauley JL, Sutcliffe JS, Ashley-Koch AE, Cuccaro ML, Folstein SE, Gilbert JR, Pericak-Vance MA. Skaar DA, et al. Among authors: ashley koch ae. Mol Psychiatry. 2005 Jun;10(6):563-71. doi: 10.1038/sj.mp.4001614. Mol Psychiatry. 2005. PMID: 15558079 Clinical Trial.
An autosomal genomic screen for dementia in an extended Amish family.
Ashley-Koch AE, Shao Y, Rimmler JB, Gaskell PC, Welsh-Bohmer KA, Jackson CE, Scott WK, Haines JL, Pericak-Vance MA. Ashley-Koch AE, et al. Neurosci Lett. 2005 May 13;379(3):199-204. doi: 10.1016/j.neulet.2004.12.065. Neurosci Lett. 2005. PMID: 15843063
256 results