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Items: 1 to 50 of 67

1.

Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese.

Gratten J, Zhao Q, Benyamin B, Garton F, He J, Leo PJ, Mangelsdorf M, Anderson L, Zhang ZH, Chen L, Chen XD, Cremin K, Deng HW, Edson J, Han YY, Harris J, Henders AK, Jin ZB, Li Z, Lin Y, Liu X, Marshall M, Mowry BJ, Ran S, Reutens DC, Song S, Tan LJ, Tang L, Wallace RH, Wheeler L, Wu J, Yang J, Xu H, Visscher PM, Bartlett PF, Brown MA, Wray NR, Fan D.

Genome Med. 2017 Nov 17;9(1):97. doi: 10.1186/s13073-017-0487-0.

2.

Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.

Benyamin B, He J, Zhao Q, Gratten J, Garton F, Leo PJ, Liu Z, Mangelsdorf M, Al-Chalabi A, Anderson L, Butler TJ, Chen L, Chen XD, Cremin K, Deng HW, Devine M, Edson J, Fifita JA, Furlong S, Han YY, Harris J, Henders AK, Jeffree RL, Jin ZB, Li Z, Li T, Li M, Lin Y, Liu X, Marshall M, McCann EP, Mowry BJ, Ngo ST, Pamphlett R, Ran S, Reutens DC, Rowe DB, Sachdev P, Shah S, Song S, Tan LJ, Tang L, van den Berg LH, van Rheenen W, Veldink JH, Wallace RH, Wheeler L, Williams KL, Wu J, Wu X, Yang J, Yue W, Zhang ZH, Zhang D, Noakes PG, Blair IP, Henderson RD, McCombe PA, Visscher PM, Xu H, Bartlett PF, Brown MA, Wray NR, Fan D.

Nat Commun. 2017 Sep 20;8(1):611. doi: 10.1038/s41467-017-00471-1.

3.

Multiplex families with epilepsy: Success of clinical and molecular genetic characterization.

Afawi Z, Oliver KL, Kivity S, Mazarib A, Blatt I, Neufeld MY, Helbig KL, Goldberg-Stern H, Misk AJ, Straussberg R, Walid S, Mahajnah M, Lerman-Sagie T, Ben-Zeev B, Kahana E, Masalha R, Kramer U, Ekstein D, Shorer Z, Wallace RH, Mangelsdorf M, MacPherson JN, Carvill GL, Mefford HC, Jackson GD, Scheffer IE, Bahlo M, Gecz J, Heron SE, Corbett M, Mulley JC, Dibbens LM, Korczyn AD, Berkovic SF.

Neurology. 2016 Feb 23;86(8):713-22. doi: 10.1212/WNL.0000000000002404. Epub 2016 Jan 22.

4.

ALS-associated TDP-43 induces endoplasmic reticulum stress, which drives cytoplasmic TDP-43 accumulation and stress granule formation.

Walker AK, Soo KY, Sundaramoorthy V, Parakh S, Ma Y, Farg MA, Wallace RH, Crouch PJ, Turner BJ, Horne MK, Atkin JD.

PLoS One. 2013 Nov 29;8(11):e81170. doi: 10.1371/journal.pone.0081170. eCollection 2013.

5.

DNA variation in the SNAP25 gene confers risk to ADHD and is associated with reduced expression in prefrontal cortex.

Hawi Z, Matthews N, Wagner J, Wallace RH, Butler TJ, Vance A, Kent L, Gill M, Bellgrove MA.

PLoS One. 2013 Apr 12;8(4):e60274. doi: 10.1371/journal.pone.0060274. Print 2013.

6.

Identification of RNA bound to the TDP-43 ribonucleoprotein complex in the adult mouse brain.

Narayanan RK, Mangelsdorf M, Panwar A, Butler TJ, Noakes PG, Wallace RH.

Amyotroph Lateral Scler Frontotemporal Degener. 2013 May;14(4):252-60. doi: 10.3109/21678421.2012.734520. Epub 2012 Oct 24.

PMID:
23134510
7.

A high density linkage disequilibrium mapping in 14 noradrenergic genes: evidence of association between SLC6A2, ADRA1B and ADHD.

Hawi Z, Matthews N, Barry E, Kirley A, Wagner J, Wallace RH, Heussler HS, Vance A, Gill M, Bellgrove MA.

Psychopharmacology (Berl). 2013 Feb;225(4):895-902. doi: 10.1007/s00213-012-2875-x. Epub 2012 Sep 29.

PMID:
23052569
8.

The COMT Val158 allele is associated with impaired delayed-match-to-sample performance in ADHD.

Matthews N, Vance A, Cummins TD, Wagner J, Connolly A, Yamada J, Lockhart PJ, Panwar A, Wallace RH, Bellgrove MA.

Behav Brain Funct. 2012 May 28;8:25. doi: 10.1186/1744-9081-8-25.

9.

"Blinders, phenotype, and fashionable genetic analysis": setting the record straight for epilepsy!

Mulley JC, Heron SE, Wallace RH, Gecz J, Dibbens LM.

Epilepsia. 2011 Sep;52(9):1757-8. doi: 10.1111/j.1528-1167.2011.03054.x. No abstract available.

10.

Magnetic resonance microimaging of the spinal cord in the SOD1 mouse model of amyotrophic lateral sclerosis detects motor nerve root degeneration.

Cowin GJ, Butler TJ, Kurniawan ND, Watson C, Wallace RH.

Neuroimage. 2011 Sep 1;58(1):69-74. doi: 10.1016/j.neuroimage.2011.06.003. Epub 2011 Jun 13.

PMID:
21689764
11.

Non-invasive diffusion tensor imaging detects white matter degeneration in the spinal cord of a mouse model of amyotrophic lateral sclerosis.

Underwood CK, Kurniawan ND, Butler TJ, Cowin GJ, Wallace RH.

Neuroimage. 2011 Mar 15;55(2):455-61. doi: 10.1016/j.neuroimage.2010.12.044. Epub 2010 Dec 24.

PMID:
21185943
12.

A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome.

Bassuk AG, Wallace RH, Buhr A, Buller AR, Afawi Z, Shimojo M, Miyata S, Chen S, Gonzalez-Alegre P, Griesbach HL, Wu S, Nashelsky M, Vladar EK, Antic D, Ferguson PJ, Cirak S, Voit T, Scott MP, Axelrod JD, Gurnett C, Daoud AS, Kivity S, Neufeld MY, Mazarib A, Straussberg R, Walid S, Korczyn AD, Slusarski DC, Berkovic SF, El-Shanti HI.

Am J Hum Genet. 2008 Nov;83(5):572-81. doi: 10.1016/j.ajhg.2008.10.003. Epub 2008 Oct 30.

13.

Latent stem and progenitor cells in the hippocampus are activated by neural excitation.

Walker TL, White A, Black DM, Wallace RH, Sah P, Bartlett PF.

J Neurosci. 2008 May 14;28(20):5240-7. doi: 10.1523/JNEUROSCI.0344-08.2008.

14.

Somatic mutations in GLI3 can cause hypothalamic hamartoma and gelastic seizures.

Wallace RH, Freeman JL, Shouri MR, Izzillo PA, Rosenfeld JV, Mulley JC, Harvey AS, Berkovic SF.

Neurology. 2008 Feb 19;70(8):653-5. Epub 2007 Dec 5. No abstract available.

PMID:
18057317
15.

Generalized epilepsy with febrile seizures plus-associated sodium channel beta1 subunit mutations severely reduce beta subunit-mediated modulation of sodium channel function.

Xu R, Thomas EA, Gazina EV, Richards KL, Quick M, Wallace RH, Harkin LA, Heron SE, Berkovic SF, Scheffer IE, Mulley JC, Petrou S.

Neuroscience. 2007 Aug 10;148(1):164-74. Epub 2007 Jul 12.

PMID:
17629415
16.

Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations.

Scheffer IE, Harkin LA, Grinton BE, Dibbens LM, Turner SJ, Zielinski MA, Xu R, Jackson G, Adams J, Connellan M, Petrou S, Wellard RM, Briellmann RS, Wallace RH, Mulley JC, Berkovic SF.

Brain. 2007 Jan;130(Pt 1):100-9. Epub 2006 Oct 4.

PMID:
17020904
17.

A new clinical and molecular form of Unverricht-Lundborg disease localized by homozygosity mapping.

Berkovic SF, Mazarib A, Walid S, Neufeld MY, Manelis J, Nevo Y, Korczyn AD, Yin J, Xiong L, Pandolfo M, Mulley JC, Wallace RH.

Brain. 2005 Mar;128(Pt 3):652-8. Epub 2005 Jan 5.

PMID:
15634728
18.

Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12.

Berkovic SF, Serratosa JM, Phillips HA, Xiong L, Andermann E, Díaz-Otero F, Gómez-Garre P, Martín M, Fernández-Bullido Y, Andermann F, Lopes-Cendes I, Dubeau F, Desbiens R, Scheffer IE, Wallace RH, Mulley JC, Pandolfo M.

Epilepsia. 2004 Sep;45(9):1054-60.

19.

Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families.

Marini C, Scheffer IE, Crossland KM, Grinton BE, Phillips FL, McMahon JM, Turner SJ, Dean JT, Kivity S, Mazarib A, Neufeld MY, Korczyn AD, Harkin LA, Dibbens LM, Wallace RH, Mulley JC, Berkovic SF.

Epilepsia. 2004 May;45(5):467-78.

20.

LGI1 mutations in temporal lobe epilepsies.

Berkovic SF, Izzillo P, McMahon JM, Harkin LA, McIntosh AM, Phillips HA, Briellmann RS, Wallace RH, Mazarib A, Neufeld MY, Korczyn AD, Scheffer IE, Mulley JC.

Neurology. 2004 Apr 13;62(7):1115-9.

PMID:
15079010
21.

Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms.

Wallace RH, Hodgson BL, Grinton BE, Gardiner RM, Robinson R, Rodriguez-Casero V, Sadleir L, Morgan J, Harkin LA, Dibbens LM, Yamamoto T, Andermann E, Mulley JC, Berkovic SF, Scheffer IE.

Neurology. 2003 Sep 23;61(6):765-9.

PMID:
14504318
22.

Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation.

Marini C, Harkin LA, Wallace RH, Mulley JC, Scheffer IE, Berkovic SF.

Brain. 2003 Jan;126(Pt 1):230-40.

PMID:
12477709
23.

Altered kinetics and benzodiazepine sensitivity of a GABAA receptor subunit mutation [gamma 2(R43Q)] found in human epilepsy.

Bowser DN, Wagner DA, Czajkowski C, Cromer BA, Parker MW, Wallace RH, Harkin LA, Mulley JC, Marini C, Berkovic SF, Williams DA, Jones MV, Petrou S.

Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):15170-5. Epub 2002 Nov 1.

24.

X-linked myoclonic epilepsy with spasticity and intellectual disability: mutation in the homeobox gene ARX.

Scheffer IE, Wallace RH, Phillips FL, Hewson P, Reardon K, Parasivam G, Stromme P, Berkovic SF, Gecz J, Mulley JC.

Neurology. 2002 Aug 13;59(3):348-56.

PMID:
12177367
25.

Generalized epilepsy with febrile seizures plus: mutation of the sodium channel subunit SCN1B.

Wallace RH, Scheffer IE, Parasivam G, Barnett S, Wallace GB, Sutherland GR, Berkovic SF, Mulley JC.

Neurology. 2002 May 14;58(9):1426-9.

PMID:
12011299
26.

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy.

Strømme P, Mangelsdorf ME, Shaw MA, Lower KM, Lewis SM, Bruyere H, Lütcherath V, Gedeon AK, Wallace RH, Scheffer IE, Turner G, Partington M, Frints SG, Fryns JP, Sutherland GR, Mulley JC, Gécz J.

Nat Genet. 2002 Apr;30(4):441-5. Epub 2002 Mar 11.

PMID:
11889467
27.

Truncation of the GABA(A)-receptor gamma2 subunit in a family with generalized epilepsy with febrile seizures plus.

Harkin LA, Bowser DN, Dibbens LM, Singh R, Phillips F, Wallace RH, Richards MC, Williams DA, Mulley JC, Berkovic SF, Scheffer IE, Petrou S.

Am J Hum Genet. 2002 Feb;70(2):530-6. Epub 2001 Dec 17.

28.

Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures.

Wallace RH, Marini C, Petrou S, Harkin LA, Bowser DN, Panchal RG, Williams DA, Sutherland GR, Mulley JC, Scheffer IE, Berkovic SF.

Nat Genet. 2001 May;28(1):49-52.

PMID:
11326275
29.

The relationship between cigarette smoking and dental implant failure.

Wallace RH.

Eur J Prosthodont Restor Dent. 2000 Sep;8(3):103-6.

PMID:
11307562
30.

Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus.

Wallace RH, Scheffer IE, Barnett S, Richards M, Dibbens L, Desai RR, Lerman-Sagie T, Lev D, Mazarib A, Brand N, Ben-Zeev B, Goikhman I, Singh R, Kremmidiotis G, Gardner A, Sutherland GR, George AL Jr, Mulley JC, Berkovic SF.

Am J Hum Genet. 2001 Apr;68(4):859-65. Epub 2001 Mar 13.

31.

Locus for febrile seizures.

Scheffer IE, Wallace RH, Mulley JC, Berkovic SF.

Ann Neurol. 2000 Jun;47(6):840-1. No abstract available.

PMID:
10852560
32.

Familial partial epilepsy with variable foci: a new partial epilepsy syndrome with suggestion of linkage to chromosome 2.

Scheffer IE, Phillips HA, O'Brien CE, Saling MM, Wrennall JA, Wallace RH, Mulley JC, Berkovic SF.

Ann Neurol. 1998 Dec;44(6):890-9.

PMID:
9851433
33.

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.

Wallace RH, Wang DW, Singh R, Scheffer IE, George AL Jr, Phillips HA, Saar K, Reis A, Johnson EW, Sutherland GR, Berkovic SF, Mulley JC.

Nat Genet. 1998 Aug;19(4):366-70.

PMID:
9697698
34.

Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21.

Wallace RH, Berkovic SF, Howell RA, Sutherland GR, Mulley JC.

J Med Genet. 1996 Apr;33(4):308-12.

35.

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.

Steinlein OK, Mulley JC, Propping P, Wallace RH, Phillips HA, Sutherland GR, Scheffer IE, Berkovic SF.

Nat Genet. 1995 Oct;11(2):201-3.

PMID:
7550350
36.
37.

Use of liquid vs. capsule form 131I.

Wallace RH.

Health Phys. 1989 Jun;56(6):963-4. No abstract available.

PMID:
2722524
38.

Radiation protection and the electron microscope.

Wallace RH, Dapolito JA.

Health Phys. 1973 Mar;24(3):355-7. No abstract available.

PMID:
4691645
39.

The relationship between encapsulation and apparent fast neutron-induced fading in TLD.

Wallace RH, Ziemer PL, Kastner J, Oltman BG.

Health Phys. 1971 Feb;20(2):221-4. No abstract available.

PMID:
5580426
40.

Absence of Seed Dormancy in a White Mutant Strain of Helianthus annuus L.

Wallace RH, Habermann HM.

Plant Physiol. 1958 Jul;33(4):252-4. No abstract available.

41.

Oxidation of compounds in the Krebs cycle by Pullularia pullulans.

CLARK DS, WALLACE RH.

Can J Microbiol. 1958 Apr;4(2):125-39. No abstract available.

PMID:
13523455
42.

Carbohydrate metabolism of Pullularia pullulans.

CLARK DS, WALLACE RH.

Can J Microbiol. 1958 Feb;4(1):43-54. No abstract available.

PMID:
13500268
43.

Correlation between bacterial numbers and organic matter in a field soil.

GRAY PH, WALLACE RH.

Can J Microbiol. 1957 Aug;3(5):711-4. No abstract available.

PMID:
13460818
44.

Morphological and physiological groups of soil bacteria from the roots of barley and oats.

KING HD, WALLACE RH.

Can J Microbiol. 1956 Aug;2(5):473-81. No abstract available.

PMID:
13364742
45.

Candida malicola, nov. sp., isolated from apples.

CLARK DS, WALLACE RH.

Can J Microbiol. 1955 Feb;1(4):275-6. No abstract available.

PMID:
14364352
46.

Yeasts occurring on apples and in apple cider.

CLARK DS, WALLACE RH, DAVID JJ.

Can J Microbiol. 1954 Dec;1(3):145-9. No abstract available.

PMID:
14352050
47.

Factors affecting the fermentation of apple juice.

CLARK DS, WALLACE RH, DAVID JJ.

Appl Microbiol. 1954 Nov;2(6):344-8. No abstract available.

48.

A Study of Chlorophyll in a White Mutant Strain of Helianthus annuus.

Wallace RH, Schwarting AE.

Plant Physiol. 1954 Sep;29(5):431-6. No abstract available.

49.

A direct method for counting bacteria in feces.

WALLACE RH.

J Bacteriol. 1952 Oct;64(4):593-4. No abstract available.

50.

Carcinoma of the breast; fifty years experience at the Massachusetts General Hospital.

TAYLOR GW, WALLACE RH.

Ann Surg. 1950 Oct;132(4):833-43. No abstract available.

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