arrow
返回
R

Ruth K. Abramson

consiglio nazionale delle ricerche (cnr)

43H指数
119论文数
7.9K被引数
收录论文 25
发表时间
Three Brothers With Autism Carry a Stop-Gain Mutation in the HPA-Axis Gene NR3C2
err2020-02-17
err7
PREAI
errCukier, 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.
err分享
err收藏
A low-cost socially assistive robot and robot-assisted intervention for children with autism spectrum disorder: field trials and lessons learned
err2016-02-23
err65
PREAI
errBoccanfuso, Laura; Scarborough, Sarah; Abramson, Ruth K.; Hall, Alicia V.; Wright, Harry H.; O'Kane, Jason M.
err分享
err收藏
The Expanding Role of MBD Genes in Autism: Identification of a MECP2 Duplication and Novel Alterations in MBD5, MBD6, and SETDB1
err2012-10-10
err87
errOAAI
errCukier, 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.
err分享
err收藏
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways
err2012-04-27
err163
errOAAI
errGriswold, Anthony J.; Ma, Deqiong; Cukier, Holly N.; Nations, Laura D.; Schmidt, Mike A.; Chung, Ren-Hua; Jaworski, James M.; Salyakina, Daria; Konidari, Ioanna; Whitehead, Patrice L.; Wright, Harry H.; Abramson, Ruth K.; Williams, Scott M.; Menon, Ramkumar; Martin, Eden R.; Haines, Jonathan L.; Gilbert, John R.; Cuccaro, Michael L.; Pericak-Vance, Margaret A.
err分享
err收藏
Common SNP-Based Haplotype Analysis of the 4p16.3 Huntington Disease Gene Region
err2012-03-01
err56
errOAAI
errLee, Jong-Min; Gillis, Tammy; Mysore, Jayalakshmi Srinidhi; Ramos, Eliana Marisa; Myers, Richard H.; Hayden, Michael R.; Morrison, Patrick J.; Nance, Martha; Ross, Christopher A.; Margolis, Russell L.; Squitieri, Ferdinando; Griguoli, Annamaria; Di Donato, Stefano; Gomez-Tortosa, Estrella; Ayuso, Carmen; Suchowersky, Oksana; Trent, Ronald J.; McCusker, Elizabeth; Novelletto, Andrea; Frontali, Marina; Jones, Randi; Ashizawa, Tetsuo; Frank, Samuel; Saint-Hilaire, Marie-Helene; Hersch, Steven M.; Rosas, Herminia D.; Lucente, Diane; Harrison, Madaline B.; Zanko, Andrea; Abramson, Ruth K.; Marder, Karen; Sequeiros, Jorge; MacDonald, Marcy E.; Gusella, James F.
err分享
err收藏
Exploring the Relationship Between Autism Spectrum Disorder and Epilepsy Using Latent Class Cluster Analysis
err2011-11-22
err34
PREAI
errCuccaro, Michael L.; Tuchman, Roberto F.; Hamilton, Kara L.; Wright, Harry H.; Abramson, Ruth K.; Haines, Jonathan L.; Gilbert, John R.; Pericak-Vance, Margaret
err分享
err收藏
An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males
err2011-11-04
err16
errOAAI
errChung, Ren-Hua; Ma, Deqiong; Wang, Kai; Hedges, Dale J.; Jaworski, James M.; Gilbert, John R.; Cuccaro, Michael L.; Wright, Harry H.; Abramson, Ruth K.; Konidari, Ioanna; Whitehead, Patrice L.; Schellenberg, Gerard D.; Hakonarson, Hakon; Haines, Jonathan L.; Pericak-Vance, Margaret A.; Martin, Eden R.
err分享
err收藏
A De Novo 1.5 Mb Microdeletion on Chromosome 14q23.2-23.3 in a Patient With Autism and Spherocytosis
err2011-02-28
err45
errOAAI
errGriswold, Anthony J.; Ma, Deqiong; Sacharow, Stephanie J.; Robinson, Joycelyn L.; Jaworski, James M.; Wright, Harry H.; Abramson, Ruth K.; Lybaek, Helle; Oyen, Nina; Cuccaro, Michael L.; Gilbert, John R.; Pericak-Vance, Margaret A.
err分享
err收藏
Variants in Several Genomic Regions Associated with Asperger Disorder
err2010-12-22
err32
errOAAI
errSalyakina, D.; Ma, D. Q.; Jaworski, J. M.; Konidari, I.; Whitehead, P. L.; Henson, R.; Martinez, D.; Robinson, J. L.; Sacharow, S.; Wright, H. H.; Abramson, R. K.; Gilbert, J. R.; Cuccaro, M. L.; Pericak-Vance, M. A.
err分享
err收藏
Clinical correlates of low serum carnitine levels in hospitalized psychiatric patients
err2010-06-29
err8
PREAI
errCuturic, Miroslav; Abramson, Ruth K.; Moran, Robert R.; Hardin, James W.; Hall, Alicia V.
err分享
err收藏
Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
err2009-10-22
err479
errOAAI
errGregory, 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.
err分享
err收藏
Examination of Association to Autism of Common Genetic Variation in Genes Related to Dopamine
err2008-12-30
err30
errOAAI
errAnderson, B. M.; Schnetz-Boutaud, N.; Bartlett, J.; Wright, H. H.; Abramson, R. K.; Cuccaro, M. L.; Gilbert, J. R.; Pericak-Vance, M. A.; Haines, J. L.
err分享
err收藏
Factor analysis of the aberrant behavior checklist in individuals with autism spectrum disorders
err2006-12-21
err132
PREAI
errBrinkley, Jason; Nations, Laura; Abramson, Ruth K.; Hall, Alicia; Wright, Harry H.; Gabriels, Robin; Gilbert, John R.; Pericak-Vance, Margaret A. O.; Cuccaro, Michael L.
err分享
err收藏
Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14
err2006-12-19
err46
PREAI
errMa, D. Q.; Cuccaro, M. L.; Jaworski, J. M.; Haynes, C. S.; Stephan, D. A.; Parod, J.; Abramson, R. K.; Wright, H. H.; Gilbert, J. R.; Haines, J. L.; Pericak-Vance, M. A.
err分享
err收藏
Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism
err2005-09-01
err316
errOAAI
errMa, DQ; Whitehead, PL; Menold, MM; Martin, ER; Ashley-Koch, AE; Mei, H; Ritchie, MD; DeLong, GR; Abramson, RK; Wright, HH; Cuccaro, ML; Hussman, JP; Gilbert, JR; Pericak-Vance, MA
err分享
err收藏
Accelerated head growth in early development of individuals with autism
err2005-02-01
err170
PREAI
errDementieva, YA; Vance, DD; Donnelly, SL; Elston, LA; Wolpert, CM; Ravan, SA; DeLong, GR; Abramson, RK; Wright, HH; Cuccaro, ML
err分享
err收藏
A genome scan for modifiers of age at onset in Huntington disease:: The HD MAPS study
err2003-09-01
err128
errOAAI
errLi, JL; Hayden, MR; Almqvist, EW; Brinkman, RR; Durr, A; Dodé, C; Morrison, PJ; Suchowersky, O; Ross, CA; Margolis, RL; Rosenblatt, A; Gómez-Tortosa, E; Cabrero, DM; Novelletto, A; Frontali, M; Nance, M; Trent, RJA; McCusker, E; Jones, R; Paulsen, JS; Harrison, M; Zanko, A; Abramson, RK; Russ, AL; Knowlton, B; Djoussé, L; Mysore, JS; Tariot, S; Gusella, MF; Wheeler, VC; Atwood, LD; Cupples, LA; Saint-Hilaire, M; Cha, JHJ; Hersch, SM; Koroshetz, WJ; Gusella, JF; MacDonald, ME; Myers, RH
err分享
err收藏
Fine mapping of Autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes
err2003-03-01
err314
errOAAI
errShao, YJ; Cuccaro, ML; Hauser, ER; Raiford, KL; Menold, MM; Wolpert, CM; Ravan, SA; Elston, L; Decena, K; Donnelly, SL; Abramson, RK; Wright, HH; Delong, GR; Gilbert, JR; Pericak-Vance, MA
err分享
err收藏
Behavioral comparisons in autistic individuals from multiplex and singleton families
err2003-01-01
err28
PREAI
errCuccaro, ML; Shao, YJ; Bass, MP; Abramson, RK; Ravan, SA; Wright, HH; Wolpert, CM; Donnelly, SL; Pericak-Vance, MA
err分享
err收藏
Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder
err2002-04-01
err159
errOAAI
errShao, YJ; Raiford, KL; Wolpert, CM; Cope, HA; Ravan, SA; Ashley-Koch, AA; Abramson, RK; Wright, HH; DeLong, RG; Gilbert, JR; Cuccaro, ML; Pericak-Vance, MA
err分享
err收藏