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Sharon Minnerath

Research Profile

Physiology

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Publications

TOP 3
Anthony A Killeen; Natalya Ossina; Ronald C McGlennen; Sharon Minnerath; John Borgos; Vadim Alexandrov; Armen Sarvazyan
Protein self-organization patterns in dried serum reveal changes in B-cell disorders.
Michelle Carter; Xu Chen; Bozena Slowinska; Sharon Minnerath; sara glickstein; Lei Shi; Fabien Campagne; HAREL WEINSTEIN; M Elizabeth Ross
Crooked tail (Cd) model of human folate-responsive neural tube defects is mutated in Wnt coreceptor lipoprotein receptor-related protein 6.
Joseph G Gleeson; Sharon Minnerath; R I Kuzniecky; William B Dobyns; I D Young; M Elizabeth Ross; Christopher Walsh
Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypes.

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All Publications

2006: Anthony A Killeen; Natalya Ossina; Ronald C McGlennen; Sharon Minnerath; John Borgos; Vadim Alexandrov; Armen Sarvazyan
Protein self-organization patterns in dried serum reveal changes in B-cell disorders.
Molecular diagnosis & therapy 2006;10(6):371-80.
2005: Michelle Carter; Xu Chen; Bozena Slowinska; Sharon Minnerath; sara glickstein; Lei Shi; Fabien Campagne; HAREL WEINSTEIN; M Elizabeth Ross
Crooked tail (Cd) model of human folate-responsive neural tube defects is mutated in Wnt coreceptor lipoprotein receptor-related protein 6.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(36):12843-8.
2000: Joseph G Gleeson; Sharon Minnerath; R I Kuzniecky; William B Dobyns; I D Young; M Elizabeth Ross; Christopher Walsh
Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypes.
American journal of human genetics 2000;67(3):574-81.
1999: Joseph G Gleeson; Sharon Minnerath; JW Fox; Kristina M Allen; R F Luo; Susan E Hong; M J Berg; R Kuzniecky; Pamela Reitnauer; Renato Borgatti; A P Mira; Renzo Guerrini; Gregory L Holmes; C M Rooney; SF Berkovic; IE Scheffer; edward cooper; S Ricci; R Cusmai; Thomas Crawford; R Leroy; Eva Andermann; James W Wheless; William B Dobyns; Christopher Walsh
Characterization of mutations in the gene doublecortin in patients with double cortex syndrome.
Annals of neurology 1999;45(2):146-53.
1998: Daniela T Pilz; N Matsumoto; Sharon Minnerath; P Mills; Joseph G Gleeson; Kristina M Allen; Christopher Walsh; A J Barkovich; William B Dobyns; David Ledbetter; M Elizabeth Ross
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.
Human molecular genetics 1998;7(13):2029-37.
1998: Joseph G Gleeson; Kristina M Allen; JW Fox; E D Lamperti; SF Berkovic; IE Scheffer; edward cooper; William B Dobyns; Sharon Minnerath; M Elizabeth Ross; Christopher Walsh
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein.
Cell 1998;92(1):63-72.