OpenURL Connection Search

Select item for more details and to access through your institution.

Mutations in RIT1 cause Noonan syndrome - additional functional evidence and expanding the clinical phenotype.
Published in:
Clinical Genetics, 2016, v. 89, n. 3, p. 359, doi. 10.1111/cge.12608
By:
- Koenighofer, M.;
- Hung, C. Y.;
- McCauley, J. L.;
- Dallman, J.;
- Back, E. J.;
- Mihalek, I.;
- Gripp, K. W.;
- Sol‐Church, K.;
- Rusconi, P.;
- Zhang, Z.;
- Shi, G‐X.;
- Andres, D. A.;
- Bodamer, O. A.
Publication type:
Article
A knowledge-driven interaction analysis reveals potential neurodegenerative mechanism of multiple sclerosis susceptibility.
Published in:
Genes & Immunity, 2011, v. 12, n. 5, p. 335, doi. 10.1038/gene.2011.3
By:
- Bush, W S;
- McCauley, J L;
- DeJager, P L;
- Dudek, S M;
- Hafler, D A;
- Gibson, R A;
- Matthews, P M;
- Kappos, L;
- Naegelin, Y;
- Polman, C H;
- Hauser, S L;
- Oksenberg, J;
- Haines, J L;
- Ritchie, M D
Publication type:
Article
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis.
Published in:
Genes & Immunity, 2010, v. 11, n. 8, p. 660, doi. 10.1038/gene.2010.36
By:
- Ban, M;
- McCauley, J L;
- Zuvich, R;
- Baker, A;
- Bergamaschi, L;
- Cox, M;
- Kemppinen, A;
- D'Alfonso, S;
- Guerini, F R;
- Lechner-Scott, J;
- Dudbridge, F;
- Wason, J;
- Robertson, N P;
- De Jager, P L;
- Hafler, D A;
- Barcellos, L F;
- Ivinson, A J;
- Sexton, D;
- Oksenberg, J R;
- Hauser, S L
Publication type:
Article
Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.
Published in:
Genes & Immunity, 2009, v. 10, n. 7, p. 624, doi. 10.1038/gene.2009.53
By:
- McCauley, J. L.;
- Zuvich, R. L.;
- Bradford, Y.;
- Kenealy, S. J.;
- Schnetz-Boutaud, N.;
- Gregory, S. G.;
- Hauser, S. L.;
- Oksenberg, J. R.;
- Mortlock, D. P.;
- Pericak-Vance, M. A.;
- Haines, J. L.
Publication type:
Article
Enrichment for Northern European-derived multiple sclerosis risk alleles in Sardinia.
Published in:
Multiple Sclerosis Journal, 2015, v. 21, n. 11, p. 1396, doi. 10.1177/1352458515581872
By:
- Hadjixenofontos, A.;
- Gourraud, P. A.;
- Bakthavachalam, V.;
- Foco, L.;
- Ticca, A.;
- Bitti, P.;
- Pastorino, R.;
- Bernardinelli, L.;
- McCauley, J. L.
Publication type:
Article
Instability of finance markets.
Published in:
European Physical Journal: Special Topics, 2009, v. 178, n. 1, p. 133, doi. 10.1140/epjst/e2010-01186-2
By:
- McCauley, J. L.
Publication type:
Article
A Genome-wide Scan in an Amish Pedigree with Parkinsonism.
Published in:
Annals of Human Genetics, 2008, v. 72, n. 5, p. 621, doi. 10.1111/j.1469-1809.2008.00452.x
By:
- Lee, S. L.;
- Murdock, D. G.;
- McCauley, J. L.;
- Bradford, Y.;
- Crunk, A.;
- McFarland, L.;
- Jiang, L.;
- Wang, T.;
- Schnetz-Boutaud, N.;
- Haines, J. L.
Publication type:
Article
Inflammatory bowel disease is presenting sooner after immigration in more recent US immigrants from Cuba.
Published in:
Alimentary Pharmacology & Therapeutics, 2017, v. 46, n. 3, p. 303, doi. 10.1111/apt.14145
By:
- Damas, O. M.;
- Avalos, D. J.;
- Palacio, A. M.;
- Gomez, L.;
- Quintero, M. A.;
- Deshpande, A. R.;
- Sussman, D. A.;
- McCauley, J. L.;
- Lopez, J.;
- Schwartz, S. J.;
- Abreu, M. T.
Publication type:
Article
Analysis of the RELN gene as a genetic risk factor for autism.
Published in:
Molecular Psychiatry, 2005, v. 10, n. 6, p. 563, doi. 10.1038/sj.mp.4001614
By:
- Skaar, D. A.;
- Shao, Y.;
- Haines, J. L.;
- Stenger, J. E.;
- Jaworski, J.;
- Martin, E. R.;
- DeLong, G. R.;
- Moore, J. H.;
- McCauley, J. L.;
- Sutcliffe, J. S.;
- Ashley-Koch, A. E.;
- Cuccaro, M. L.;
- Folstein, S. E.;
- Gilbert, J. R.;
- Pericak-Vance, M. A.
Publication type:
Article
Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.
Published in:
Molecular Psychiatry, 2003, v. 8, n. 6, p. 624, doi. 10.1038/sj.mp.4001283
By:
- Nurmi, E L;
- Amin, T;
- Olson, L M;
- Jacobs, M M;
- McCauley, J L;
- Lam, A Y;
- Organ, E L;
- Folstein, S E;
- Haines, J L;
- Sutcliffe, J S
Publication type:
Article
Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.
Published in:
Molecular Psychiatry, 2003, v. 8, n. 6, p. 570, doi. 10.1038/sj.mp.4001361
By:
- Nurmi, E L;
- Amin, T;
- Olson, L M;
- Jacob, M M;
- McCauley, J L;
- Lam, A Y;
- Organ, E L;
- Folstein, S E;
- Haines, J L;
- Sutcliffe, J S
Publication type:
Article

Found: 11