Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 7

1.

Identifying autism loci and genes by tracing recent shared ancestry.

Morrow EM, Yoo SY, Flavell SW, Kim TK, Lin Y, Hill RS, Mukaddes NM, Balkhy S, Gascon G, Hashmi A, Al-Saad S, Ware J, Joseph RM, Greenblatt R, Gleason D, Ertelt JA, Apse KA, Bodell A, Partlow JN, Barry B, Yao H, Markianos K, Ferland RJ, Greenberg ME, Walsh CA.

Science. 2008 Jul 11;321(5886):218-23. doi: 10.1126/science.1157657. Erratum in: Science. 2010 Dec 24;330(6012):1746.

2.

A structural basis for reading fluency: white matter defects in a genetic brain malformation.

Chang BS, Katzir T, Liu T, Corriveau K, Barzillai M, Apse KA, Bodell A, Hackney D, Alsop D, Wong ST, Walsh CA.

Neurology. 2007 Dec 4;69(23):2146-54. Erratum in: Neurology. 2009 Mar 31;72(13):1192.. Wong, S [corrected to Wong, ST].

PMID:
18056578
3.

The role of RELN in lissencephaly and neuropsychiatric disease.

Chang BS, Duzcan F, Kim S, Cinbis M, Aggarwal A, Apse KA, Ozdel O, Atmaca M, Zencir S, Bagci H, Walsh CA.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jan 5;144B(1):58-63.

PMID:
16958033
4.

A familial syndrome of unilateral polymicrogyria affecting the right hemisphere.

Chang BS, Apse KA, Caraballo R, Cross JH, Mclellan A, Jacobson RD, Valente KD, Barkovich AJ, Walsh CA.

Neurology. 2006 Jan 10;66(1):133-5.

PMID:
16401865
5.

Living with Marfan syndrome: coping with stigma.

Peters K, Apse K, Blackford A, McHugh B, Michalic D, Biesecker B.

Clin Genet. 2005 Jul;68(1):6-14.

PMID:
15952980
6.

Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia.

Chang BS, Ly J, Appignani B, Bodell A, Apse KA, Ravenscroft RS, Sheen VL, Doherty MJ, Hackney DB, O'Connor M, Galaburda AM, Walsh CA.

Neurology. 2005 Mar 8;64(5):799-803.

PMID:
15753412
7.

Perceptions of genetic discrimination among at-risk relatives of colorectal cancer patients.

Apse KA, Biesecker BB, Giardiello FM, Fuller BP, Bernhardt BA.

Genet Med. 2004 Nov-Dec;6(6):510-6.

PMID:
15545747

Supplemental Content

Loading ...
Support Center