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Published in:
Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 2, p. N.PAG, doi. 10.1002/mgg3.1169
By:
- Akler, Gidon;
- Birch, Ashley H.;
- Schreiber‐Agus, Nicole;
- Cai, Xiaoqiang;
- Cai, Guiqing;
- Shi, Lisong;
- Yu, Chunli;
- Larmore, Anastasia M.;
- Mendiratta‐Vij, Geetu;
- Elkhoury, Lama;
- Dillon, Mitchell W.;
- Zhu, Jun;
- Mclellan, Andrew S.;
- Suer, Funda E.;
- Webb, Bryn D.;
- Schadt, Eric E.;
- Kornreich, Ruth;
- Edelmann, Lisa
Publication type:
Article
Lessons learned from expanded reproductive carrier screening in self‐reported Ashkenazi, Sephardi, and Mizrahi Jewish patients.
Published in:
Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 2, p. N.PAG, doi. 10.1002/mgg3.1053
By:
- Akler, Gidon;
- Birch, Ashley H.;
- Schreiber‐Agus, Nicole;
- Cai, Xiaoqiang;
- Cai, Guiqing;
- Shi, Lisong;
- Yu, Chunli;
- Larmore, Anastasia M.;
- Mendiratta‐Vij, Geetu;
- Elkhoury, Lama;
- Dillon, Mitchell W.;
- Zhu, Jun;
- Mclellan, Andrew S.;
- Suer, Funda E.;
- Webb, Bryn D.;
- Schadt, Eric E.;
- Kornreich, Ruth;
- Edelmann, Lisa
Publication type:
Article
Dementia revealed: Novel chromosome 6 locus for late-onset Alzheimer's disease provides genetic evidence for folate-pathway abnormalities
Published in:
2010
By:
- Naj, Adam C.;
- Beecham, Gary W.;
- Martin, Eden R.;
- Gallins, Paul J.;
- Powell, Eric H.;
- Konidari, Ioanna;
- Whitehead, Patrice L.;
- Cai, Guiqing;
- Kajiwara, Yuji;
- Haroutunian, Vahram;
- Scott, William K.;
- Vance, Jeffery M.;
- Slifer, Michael A.;
- Gwirtsman, Harry E.;
- Gilbert, John R.;
- Haines, Jonathan L.;
- Buxbaum, Joseph D.;
- Pericak-Vance, Margaret A.
Publication type:
Abstract
ELAVL4 locus confirmed in depression of Alzheimer's disease
Published in:
2009
By:
- Slifer, Michael A.;
- Naj, Adam;
- Beecham, Gary;
- Martin, Eden;
- Konidari, Ioanna;
- Whitehead, Patrice;
- Gallins, Paul;
- Cai, Guiqing;
- Kajiwara, Yuji;
- Haroutunian, Vahram;
- Vance, Jeffery;
- Haines, Jonathan;
- Buxbaum, Joseph;
- Pericak-Vance, Margaret
Publication type:
Abstract
Genome-wide association study validates associations in APOE, VDR, SORL1, WWC1, and ELAVL4 and identifies novel candidate genes for late-onset Alzheimer's disease
Published in:
2009
By:
- Naj, Adam C.;
- Beecham, Gary W.;
- Slifer, Michael A.;
- Martin, Eden R.;
- Gallins, Paul J.;
- Konidari, Ioanna;
- Whitehead, Patrice L.;
- Cai, Guiqing;
- Kajiwara, Yuji;
- Haroutunian, Vahram;
- Gwirtsman, Harry E.;
- Gilbert, John R.;
- Haines, Jonathan L.;
- Buxbaum, Joseph D.;
- Pericak-Vance, Margaret A.
Publication type:
Abstract
GRB-associated binding protein 2 (GAB2) interacts with APOE to alter risk of late-onset Alzheimer's disease
Published in:
2009
By:
- Beecham, Gary W.;
- Naj, Adam C.;
- Cai, Guiqing;
- Kajiwara, Yuji;
- Haroutunian, Vahram;
- Konidari, Ioanna;
- Gallins, Paul;
- Whitehead, Patrice;
- Gilbert, John R.;
- Slifer, Michael A.;
- Gwirstman, Harry;
- Martin, Eden R.;
- Buxbaum, Joseph;
- Haines, Jonathan L.;
- Pericak-Vance, Margaret A.
Publication type:
Abstract
No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set.
Published in:
Autism Research: Official Journal of the International Society for Autism Research, 2011, v. 4, n. 4, p. 293, doi. 10.1002/aur.195
By:
- Allen-Brady, Kristina;
- Cai, Guiqing;
- Cannon, Dale;
- Robison, Reid;
- McMahon, William M.;
- Coon, Hilary;
- Buxbaum, Joseph D.
Publication type:
Article
A large-scale screen for coding variants in SERT/ SLC6A4 in autism spectrum disorders.
Published in:
Autism Research: Official Journal of the International Society for Autism Research, 2008, v. 1, n. 4, p. 251, doi. 10.1002/aur.30
By:
- Sakurai, Takeshi;
- Reichert, Jennifer;
- Hoffman, Ellen J.;
- Cai, Guiqing;
- Jones, Hywel B.;
- Faham, Malek;
- Buxbaum, Joseph D.
Publication type:
Article
Characterization of <i>SLITRK1</i> Variation in Obsessive-Compulsive Disorder.
Published in:
PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0070376
By:
- Ozomaro, Uzoezi;
- Cai, Guiqing;
- Kajiwara, Yuji;
- Yoon, Seungtai;
- Makarov, Vladimir;
- Delorme, Richard;
- Betancur, Catalina;
- Ruhrmann, Stephan;
- Falkai, Peter;
- Grabe, Hans Jörgen;
- Maier, Wolfgang;
- Wagner, Michael;
- Lennertz, Leonhard;
- Moessner, Rainald;
- Murphy, Dennis L.;
- Buxbaum, Joseph D.;
- Züchner, Stephan;
- Grice, Dorothy E.
Publication type:
Article
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Published in:
Nature, 2009, v. 459, n. 7246, p. 569, doi. 10.1038/nature07953
By:
- Glessner, Joseph T.;
- Wang, Kai;
- Cai, Guiqing;
- Korvatska, Olena;
- Kim, Cecilia E.;
- Wood, Shawn;
- Zhang, Haitao;
- Estes, Annette;
- Brune, Camille W.;
- Bradfield, Jonathan P.;
- Imielinski, Marcin;
- Frackelton, Edward C.;
- Reichert, Jennifer;
- Crawford, Emily L.;
- Munson, Jeffrey;
- Sleiman, Patrick M. A.;
- Chiavacci, Rosetta;
- Annaiah, Kiran;
- Thomas, Kelly;
- Hou, Cuiping
Publication type:
Article
Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.
Published in:
Molecular Autism, 2013, v. 4, n. 1, p. 1, doi. 10.1186/2040-2392-4-18
By:
- Soorya, Latha;
- Kolevzon, Alexander;
- Zweifach, Jessica;
- Lim, Teresa;
- Dobry, Yuriy;
- Schwartz, Lily;
- Frank, Yitzchak;
- Ting Wang, A.;
- Cai, Guiqing;
- Parkhomenko, Elena;
- Halpern, Danielle;
- Grodberg, David;
- Angarita, Benjamin;
- Willner, Judith P.;
- Yang, Amy;
- Canitano, Roberto;
- Chaplin, William;
- Betancur, Catalina;
- Buxbaum, Joseph D.
Publication type:
Article
Genetic markers for PTSD risk and resilience among survivors of the World Trade Center attacks.
Published in:
Disease Markers, 2011, v. 30, n. 2-3, p. 101
By:
- Yehuda, Rachel;
- Sarapas, Casey;
- Cai, Guiqing;
- Bierer, Linda M.;
- Golier, Julia A.;
- Galea, Sandro;
- Ising, Marcus;
- Rein, Theo;
- Schmeidler, James;
- Müller-Myhsok, Bertram;
- Uhr, Manfred;
- Holsboer, Florian;
- Buxbaum, Joseph D.
Publication type:
Article
Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis.
Published in:
Human Molecular Genetics, 2015, v. 24, n. 14, p. 4006, doi. 10.1093/hmg/ddv138
By:
- Kozol, Robert A.;
- Cukier, Holly N.;
- Bing Zou;
- Mayo, Vera;
- De Rubeis, Silvia;
- Cai, Guiqing;
- Griswold, Anthony J.;
- Whitehead, Patrice L.;
- Haines, Jonathan L.;
- Gilbert, John R.;
- Cuccaro, Michael L.;
- Martin, Eden R.;
- Baker, James D.;
- Buxbaum, Joseph D.;
- Pericak-Vance, Margaret A.;
- Dallman, Julia E.
Publication type:
Article
AnnTools: a comprehensive and versatile annotation toolkit for genomic variants.
Published in:
Bioinformatics, 2012, v. 28, n. 5, p. 724, doi. 10.1093/bioinformatics/bts032
By:
- Makarov, Vladimir;
- O'Grady, Tina;
- Cai, Guiqing;
- Lihm, Jayon;
- Buxbaum, Joseph D.;
- Yoon, Seungtai
Publication type:
Article
De novo SCN2A splice site mutation in a boy with Autism spectrum disorder.
Published in:
BMC Medical Genetics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2350-15-35
By:
- Tavassoli, Teresa;
- Kolevzon, Alexander;
- Wang, A. Ting;
- Curchack-Lichtin, Jocelyn;
- Halpern, Danielle;
- Schwartz, Lily;
- Soffes, Sarah;
- Bush, Lauren;
- Grodberg, David;
- Guiqing Cai;
- Buxbaum, Joseph D.
Publication type:
Article
Mutation analysis of the NSD1 gene in patients with autismspectrum disorders and macrocephaly.
Published in:
BMC Medical Genetics, 2007, v. 8, p. 68, doi. 10.1186/1471-2350-8-68
By:
- Buxbaum, Joseph D.;
- Cai, Guiqing;
- Nygren, Gudrun;
- Chaste, Pauline;
- Delorme, Richard;
- Goldsmith, Juliet;
- Råstam, Maria;
- Silverman, Jeremy M.;
- Hollander, Eric;
- Gillberg, Christopher;
- Leboyer, Marion;
- Betancur, Catalina
Publication type:
Article

Found: 16