Report of the APOE4 National Institute on Aging/Alzheimer Disease Sequencing Project Consortium Working Group: Reducing APOE4 in Carriers is a Therapeutic Goal for Alzheimer's Dise... von Vance, Jeffery M, Farrer, Lindsay A, Huang, Yadong, Cruchaga, Carlos, Hyman, Bradley T, Pericak-Vance, Margaret A, Goate, Alison M, Greicius, Michael D, Griswold, Anthony J, Haines, Jonathan L, Tcw, Julia, Schellenberg, Gerard D, Tsai, Li-Huei, Herz, Joachim, Holtzman, David M

Volltext

Polygenic Risk Score for Alzheimer's Disease in Caribbean Hispanics von Sariya, Sanjeev, Felsky, Daniel, Reyes‐Dumeyer, Dolly, Lali, Ricky, Lantigua, Rafael A., Vardarajan, Badri, Jiménez‐Velázquez, Ivonne Z., Haines, Jonathan L., Shellenberg, Gerard D., Pericak‐Vance, Margaret A, Paré, Guillaume, Mayeux, Richard, Tosto, Giuseppe

Volltext

Assessment of intraretinal hyperreflective foci using multimodal imaging in eyes with age‐related macular degeneration von Oncel, Deniz, Corradetti, Giulia, He, Ye, Ashrafkhorasani, Maryam, Nittala, Muneeswar Gupta, Stambolian, Dwight, Pericak‐Vance, Margaret A., Haines, Jonathan L., Sadda, Srinivas R.

Volltext

DNA from multiple viral species is associated with Alzheimer's disease risk von Tejeda, Marlene, Farrell, John, Zhu, Congcong, Wetzler, Lee, Lunetta, Kathryn L., Bush, William S., Martin, Eden R., Wang, Li‐San, Schellenberg, Gerard D., Pericak‐Vance, Margaret A., Haines, Jonathan L., Farrer, Lindsay A., Sherva, Richard

Volltext

Psychometric approaches to defining cognitive phenotypes in the Old Order Amish von Zaman, Andrew, Caywood, Laura, Prough, Michael, Clouse, Jason, Harrington, Sharlene, Adams, Larry, Fuzzell, Denise, Fuzzell, Sarada, Laux, Renee, Hochstetler, Sherri D., Ogrocki, Paula, Lerner, Alan, Vance, Jeffery M., Haines, Jonathan L., Scott, William K., Pericak‐Vance, Margaret A., Cuccaro, Michael L.

Volltext

Neuropsychiatric features in a multi‐ethnic population with Alzheimer disease and mild cognitive impairment von Celis, Katrina, Zaman, Andrew, Adams, Larry Deon, Gardner, Olivia, Farid, Rajabli, Starks, Takiyah D., Lacroix, Faina C., Hamilton‐Nelson, Kara, Mena, Pedro, Tejada, Sergio, Laux, Renee, Song, Yeunjoo E., Caban‐Holt, Allison, Feliciano‐Astacio, Briseida, Vance, Jeffery M., Haines, Jonathan L., Byrd, Goldie S., Beecham, Gary W., Pericak‐Vance, Margaret A., Cuccaro, Michael L.

Volltext

Coronary collateralization shows sex and racial-ethnic differences in obstructive artery disease patients von Liu, Zhi, Pericak-Vance, Margaret A, Goldschmidt-Clermont, Pascal, Seo, David, Wang, Liyong, Rundek, Tatjana, Beecham, Gary W

Volltext

One for all and all for One: Improving replication of genetic studies through network diffusion von Lancour, Daniel, Naj, Adam, Mayeux, Richard, Haines, Jonathan L, Pericak-Vance, Margaret A, Schellenberg, Gerard D, Crovella, Mark, Farrer, Lindsay A, Kasif, Simon

Volltext

Longitudinal change in memory performance as a strong endophenotype for Alzheimer's disease von Archer, Derek B., Eissman, Jaclyn M., Mukherjee, Shubhabrata, Lee, Michael L., Choi, Seo‐Eun, Scollard, Phoebe, Trittschuh, Emily H., Mez, Jesse B., Bush, William S., Kunkle, Brian W., Naj, Adam C., Gifford, Katherine A., Cuccaro, Michael L., Pericak‐Vance, Margaret A., Farrer, Lindsay A., Wang, Li‐San, Schellenberg, Gerard D., Mayeux, Richard P., Haines, Jonathan L., Jefferson, Angela L., Kukull, Walter A., Keene, C. Dirk, Saykin, Andrew J., Thompson, Paul M., Martin, Eden R., Bennett, David A., Barnes, Lisa L., Schneider, Julie A., Crane, Paul K., Dumitrescu, Logan, Hohman, Timothy J.

Volltext

Sex‐specific genetic architecture of late‐life memory performance von Eissman, Jaclyn M., Archer, Derek B., Mukherjee, Shubhabrata, Lee, Michael L., Choi, Seo‐Eun, Scollard, Phoebe, Trittschuh, Emily H., Mez, Jesse B., Bush, William S., Kunkle, Brian W., Naj, Adam C., Gifford, Katherine A., Cuccaro, Michael L., Cruchaga, Carlos, Pericak‐Vance, Margaret A., Farrer, Lindsay A., Wang, Li‐San, Schellenberg, Gerard D., Mayeux, Richard P., Haines, Jonathan L., Jefferson, Angela L., Kukull, Walter A., Keene, C. Dirk, Saykin, Andrew J., Thompson, Paul M., Martin, Eden R., Bennett, David A., Barnes, Lisa L., Schneider, Julie A., Crane, Paul K., Hohman, Timothy J., Dumitrescu, Logan

Volltext

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia von Deng, Han-Xiang, Chen, Wenjie, Hong, Seong-Tshool, Boycott, Kym M., Gorrie, George H., Siddique, Nailah, Yang, Yi, Fecto, Faisal, Shi, Yong, Zhai, Hong, Jiang, Hujun, Hirano, Makito, Rampersaud, Evadnie, Jansen, Gerard H., Donkervoort, Sandra, Bigio, Eileen H., Brooks, Benjamin R., Ajroud, Kaouther, Sufit, Robert L., Haines, Jonathan L., Mugnaini, Enrico, Pericak-Vance, Margaret A., Siddique, Teepu

Volltext

Factor Analysis of the Aberrant Behavior Checklist in Individuals with Autism Spectrum Disorders von Brinkley, Jason, Nations, Laura, Abramson, Ruth K, Hall, Alicia, Wright, Harry H, Gabriels, Robin, Gilbert, John R, Pericak-Vance, Margaret A. O, Cuccaro, Michael L

Volltext

Three Brothers With Autism Carry a Stop‐Gain Mutation in the HPA‐Axis Gene NR3C2 von Cukier, Holly N., Griswold, Anthony J., Hofmann, Natalia K., Gomez, Lissette, Whitehead, Patrice L., Abramson, Ruth K., Gilbert, John R., Cuccaro, Michael L., Dykxhoorn, Derek M., Pericak‐Vance, Margaret A.

Volltext

Family History of Eating Disorder and the Broad Autism Phenotype in Autism von Barrionuevo, Bianca A., Chowdhury, Aneesa R., Lee, Joycelyn M., Dueker, Nicole D., Martin, Eden R., Pericak‐Vance, Margaret A., Cuccaro, Michael

Volltext

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism von Hussman, John P, Chung, Ren-Hua, Griswold, Anthony J, Jaworski, James M, Salyakina, Daria, Ma, Deqiong, Konidari, Ioanna, Whitehead, Patrice L, Vance, Jeffery M, Martin, Eden R, Cuccaro, Michael L, Gilbert, John R, Haines, Jonathan L, Pericak-Vance, Margaret A

Volltext

Identification of TMEM230 mutations in familial Parkinson's disease von Deng, Han-Xiang, Shi, Yong, Yang, Yi, Ahmeti, Kreshnik B, Miller, Nimrod, Huang, Cao, Cheng, Lijun, Zhai, Hong, Deng, Sheng, Nuytemans, Karen, Corbett, Nicola J, Kim, Myung Jong, Deng, Hao, Tang, Beisha, Yang, Ziquang, Xu, Yanming, Chan, Piu, Huang, Bo, Gao, Xiao-Ping, Song, Zhi, Liu, Zhenhua, Fecto, Faisal, Siddique, Nailah, Foroud, Tatiana, Jankovic, Joseph, Ghetti, Bernardino, Nicholson, Daniel A, Krainc, Dimitri, Melen, Onur, Vance, Jeffery M, Pericak-Vance, Margaret A, Ma, Yong-Chao, Rajput, Ali H, Siddique, Teepu

Volltext

Causal Associations Between Modifiable Risk Factors and the Alzheimer's Phenome von Andrews, Shea J., Fulton‐Howard, Brian, O'Reilly, Paul, Marcora, Edoardo, Goate, Alison M., Farrer, Lindsay A., Haines, Jonathan L., Mayeux, Richard, Naj, Adam C., Pericak‐Vance, Margaret A., Schellenberg, Gerard D., Wang, Li‐San

Volltext

Neuropathological lesions and their contribution to dementia and cognitive impairment in a heterogeneous clinical population von Godrich, Dana, Martin, Eden R., Schellenberg, Gerard, Pericak‐Vance, Margaret A., Cuccaro, Michael, Scott, William K., Kukull, Walter, Montine, Thomas, Beecham, Gary W.

Volltext

The Expanding Role of MBD Genes in Autism: Identification of a MECP2 Duplication and Novel Alterations in MBD5, MBD6, and SETDB1 von Cukier, Holly N., Lee, Joycelyn M., Ma, Deqiong, Young, Juan I., Mayo, Vera, Butler, Brittany L., Ramsook, Sandhya S., Rantus, Joseph A., Abrams, Alexander J., Whitehead, Patrice L., Wright, Harry H., Abramson, Ruth K., Haines, Jonathan L., Cuccaro, Michael L., Pericak-Vance, Margaret A., Gilbert, John R.

Volltext

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism von Gregory, Simon G, Connelly, Jessica J, Towers, Aaron J, Johnson, Jessica, Biscocho, Dhani, Markunas, Christina A, Lintas, Carla, Abramson, Ruth K, Wright, Harry H, Ellis, Peter, Langford, Cordelia F, Worley, Gordon, Delong, G Robert, Murphy, Susan K, Cuccaro, Michael L, Persico, Antonello, Pericak-Vance, Margaret A

Volltext