Flow Residence Time and Regions of Intraluminal Thrombus Deposition in Intracranial Aneurysms
Rayz, V. L, Boussel, L, Ge, L, Leach, J. R, Martin, A. J, Lawton, M. T, McCulloch, C, Saloner, D
Published in Annals of biomedical engineering (01.10.2010)
Published in Annals of biomedical engineering (01.10.2010)
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A novel potassium channel gene, KCNQ2 , is mutated in an inherited epilepsy of newborns
Singh, Nanda A, Charlier, Carole, Stauffer, Dora, DuPont, Barbara R, Leach, Robin J, Melis, Roberta, Ronen, Gabriel M, Bjerre, Ingrid, Quattlebaum, Thomas, Murphy, Jerome V, McHarg, Malcolm L, Gagnon, David, Rosales, Teodoro O, Peiffer, Andy, Anderson, V. Elving, Leppert, Mark
Published in Nature genetics (01.01.1998)
Published in Nature genetics (01.01.1998)
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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
Charlier, C, Singh, N A, Ryan, S G, Lewis, T B, Reus, B E, Leach, R J, Leppert, M
Published in Nature genetics (01.01.1998)
Published in Nature genetics (01.01.1998)
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Linkage of Type 2 Diabetes Mellitus and of Age at Onset to a Genetic Location on Chromosome 10q in Mexican Americans
Duggirala, Ravindranath, Blangero, John, Almasy, Laura, Dyer, Thomas D., Williams, Kenneth L., Leach, Robin J., O'Connell, Peter, Stern, Michael P.
Published in American journal of human genetics (01.04.1999)
Published in American journal of human genetics (01.04.1999)
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Association analyses of the neuregulin 1 gene with schizophrenia and manic psychosis in a Hispanic population
Walss-Bass, C., Raventos, H., Montero, A. P., Armas, R., Dassori, A., Contreras, S., Liu, W., Medina, R., Levinson, D. F., Pereira, M., Leach, R. J., Almasy, L., Escamilla, M. A.
Published in Acta psychiatrica Scandinavica (01.04.2006)
Published in Acta psychiatrica Scandinavica (01.04.2006)
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TGFB-induced factor (TGIF): a candidate gene for psychosis on chromosome 18p
CHAVARRIA-SILES, I, WALSS-BASS, C, RAVENTOS, H, ESCAMILLA, M. A, QUEZADA, P, DASSORI, A, CONTRERAS, S, MEDINA, R, RAMIREZ, M, ARMAS, R, SALAZAR, R, LEACH, R. J
Published in Molecular psychiatry (01.11.2007)
Published in Molecular psychiatry (01.11.2007)
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Genetic Linkage of Paget Disease of the Bone to Chromosome 18q
Cody, J.D., Singer, F.R., Roodman, G.D., Otterund, B., Lewis, T.B., Leppert, M., Leach, R.J.
Published in American journal of human genetics (01.11.1997)
Published in American journal of human genetics (01.11.1997)
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Reduced Jet Velocity in Venous Flow after CSF Drainage: Assessing Hemodynamic Causes of Pulsatile Tinnitus
Haraldsson, H, Leach, J R, Kao, E I, Wright, A G, Ammanuel, S G, Khangura, R S, Ballweber, M K, Chin, C T, Shah, V N, Meisel, K, Saloner, D A, Amans, M R
Published in American journal of neuroradiology : AJNR (01.05.2019)
Published in American journal of neuroradiology : AJNR (01.05.2019)
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Computational Modeling of Flow-Altering Surgeries in Basilar Aneurysms
Rayz, V. L., Abla, A., Boussel, L., Leach, J. R., Acevedo-Bolton, G., Saloner, D., Lawton, M. T.
Published in Annals of biomedical engineering (01.05.2015)
Published in Annals of biomedical engineering (01.05.2015)
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A Major Susceptibility Locus Influencing Plasma Triglyceride Concentrations Is Located on Chromosome 15q in Mexican Americans
Duggirala, Ravindranath, Blangero, John, Almasy, Laura, Dyer, Thomas D., Williams, Kenneth L., Leach, Robin J., O'Connell, Peter, Stern, Michael P.
Published in American journal of human genetics (01.04.2000)
Published in American journal of human genetics (01.04.2000)
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Case Report: Syndrome of Remitting Seronegative Symmetrical Synovitis with Pitting Edema—A Rare but Treatable Condition in Palliative Medicine
Moore, L Merkle, Brouner, Jennifer M, Grigorian, Nelly, Leach, R J, Baumrucker, Steven J
Published in Palliative Medicine Reports (01.12.2022)
Published in Palliative Medicine Reports (01.12.2022)
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Evaluation of tight junction protein 1 encoding zona occludens 1 as a candidate gene for albuminuria in a Mexican American population
Lehman, D M, Leach, R J, Johnson-Pais, T, Hamlington, J, Fowler, S, Almasy, L, Duggirala, R, Stern, M P, Abboud, H E
Published in Experimental and clinical endocrinology & diabetes (01.09.2006)
Published in Experimental and clinical endocrinology & diabetes (01.09.2006)
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Effects of combining transforming growth factor beta and 1,25-dihydroxyvitamin D3 on differentiation of a human osteosarcoma (MG-63)
BONEWALD, L. F, KESTER, M. B, SCHWARTZ, Z, SWAIN, L. D, KHARE, A, JOHNSON, T. L, LEACH, R. J, BOYAN, B. D
Published in The Journal of biological chemistry (05.05.1992)
Published in The Journal of biological chemistry (05.05.1992)
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Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome: evidence for myelin basic protein haploinsufficiency
Gay, C T, Hardies, L J, Rauch, R A, Lancaster, J L, Plaetke, R, DuPont, B R, Cody, J D, Cornell, J E, Herndon, R C, Ghidoni, P D, Schiff, J M, Kaye, C I, Leach, R J, Fox, P T
Published in American journal of medical genetics (25.07.1997)
Published in American journal of medical genetics (25.07.1997)
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Genetic heterogeneity in benign familial neonatal convulsions : identification of a new locus on chromosome 8q
LEWIS, T. B, LEACH, R. J, WARD, K, O'CONNELL, P, RYAN, S. G
Published in American journal of human genetics (01.09.1993)
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Published in American journal of human genetics (01.09.1993)
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How valid and accurate are measurements of golf impact parameters obtained using commercially available radar and stereoscopic optical launch monitors?
Leach, R.J., Forrester, S.E., Mears, A.C., Roberts, J.R.
Published in Measurement : journal of the International Measurement Confederation (01.12.2017)
Published in Measurement : journal of the International Measurement Confederation (01.12.2017)
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The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication
Vance, J.M, Van Broeckhoven, C, Timmerman, V, Othman, K. Ben, Nieuwenhuijsen, B.W, Chen, K.L, Wang, S, Raeymaekers, P, Van Hul, W, van Ommen, G-J.B, Hanemann, C.O, Müller, H.W, Martin, J-J, Leach, R.J, Fischbeck, K.H, De Jonghe, P, Cullen, B, Nelis, E
Published in Nature genetics (01.06.1992)
Published in Nature genetics (01.06.1992)
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Evidence for a Novel Osteosarcoma Tumor-Suppressor Gene in the Chromosome 18 Region Genetically Linked with Paget Disease of Bone
Nellissery, Maggie J., Padalecki, Susan S., Brkanac, Zoran, Singer, Frederick R., Roodman, G. David, Unni, K. Krishnan, Leach, Robin J., Hansen, Marc F.
Published in American journal of human genetics (01.09.1998)
Published in American journal of human genetics (01.09.1998)
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