Year |
Citation |
Score |
Low-probability matches (unlikely to be authored by this person) |
2006 |
Donarum EA, Stephan DA, Larkin K, Murphy EJ, Gupta M, Senephansiri H, Switzer RC, Pearl PL, Snead OC, Jakobs C, Gibson KM. Expression profiling reveals multiple myelin alterations in murine succinate semialdehyde dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 29: 143-56. PMID 16601881 DOI: 10.1007/s10545-006-0247-6 |
0.01 |
|
2006 |
Donarum EA, Halperin RF, Stephan DA, Narayanan V. Cognitive dysfunction in NF1 knock-out mice may result from altered vesicular trafficking of APP/DRD3 complex. Bmc Neuroscience. 7: 22. PMID 16524466 DOI: 10.1186/1471-2202-7-22 |
0.01 |
|
2004 |
Puffenberger EG, Hu-Lince D, Parod JM, Craig DW, Dobrin SE, Conway AR, Donarum EA, Strauss KA, Dunckley T, Cardenas JF, Melmed KR, Wright CA, Liang W, Stafford P, Flynn CR, et al. Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function. Proceedings of the National Academy of Sciences of the United States of America. 101: 11689-94. PMID 15273283 DOI: 10.1073/Pnas.0401194101 |
0.01 |
|
2002 |
Devaney JM, Donarum EA, Brown KM, Meyer J, Stöber G, Lesch KP, Nestadt G, Stephan DA, Pulver AE. No missense mutation of WKL1 in a subgroup of probands with schizophrenia. Molecular Psychiatry. 7: 419-23. PMID 11986987 DOI: 10.1038/Sj.Mp.4001022 |
0.01 |
|
2001 |
Laitinen PJ, Brown KM, Piippo K, Swan H, Devaney JM, Brahmbhatt B, Donarum EA, Marino M, Tiso N, Viitasalo M, Toivonen L, Stephan DA, Kontula K. Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia. Circulation. 103: 485-90. PMID 11157710 DOI: 10.1161/01.Cir.103.4.485 |
0.01 |
|
2001 |
Donarum EA, Brown KM, Devaney JM, Stevenson G, Stephan DA, Pulver AE. Screening of candidate Genes for schizophrenia susceptibility in chromosome 8p12-p21 American Journal of Medical Genetics - Neuropsychiatric Genetics. 105: 598. |
0.01 |
|
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