Search Results - "Menold, M. M."

Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism by Ma, D.Q., Whitehead, P.L., Menold, M.M., Martin, E.R., Ashley-Koch, A.E., Mei, H., Ritchie, M.D., DeLong, G.R., Abramson, R.K., Wright, H.H., Cuccaro, M.L., Hussman, J.P., Gilbert, J.R., Pericak-Vance, M.A.

“…Autism is a common neurodevelopmental disorder with a significant genetic component. Existing research suggests that multiple genes contribute to autism and…”
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Fine Mapping of Autistic Disorder to Chromosome 15q11-q13 by Use of Phenotypic Subtypes by Shao, Yujun, Cuccaro, M.L., Hauser, E.R., Raiford, K.L., Menold, M.M., Wolpert, C.M., Ravan, S.A., Elston, L., Decena, K., Donnelly, S.L., Abramson, R.K., Wright, H.H., DeLong, G.R., Gilbert, J.R., Pericak-Vance, M.A.

“…Autistic disorder (AutD) is a complex genetic disease. Available evidence suggests that several genes contribute to the underlying genetic risk for the…”
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novel role for Lsc/p115 RhoGEF and LARG in regulating RhoA activity downstream of adhesion to fibronectin by Dubash, Adi D, Wennerberg, Krister, García-Mata, Rafael, Menold, Marisa M, Arthur, William T, Burridge, Keith

“…Adhesion of cells to extracellular matrix proteins such as fibronectin initiates signaling cascades that affect cell morphology, migration and survival. Some…”
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Genomic screen and follow-up analysis for autistic disorder by Shao, Yujun, Wolpert, Chantelle M., Raiford, Kimberly L., Menold, Marisa M., Donnelly, Shannon L., Ravan, Sarah A., Bass, Meredyth P., McClain, Cate, von Wendt, Lennart, Vance, Jeffery M., Abramson, Ruth H., Wright, Harry H., Ashley-Koch, Allison, Gilbert, John R., DeLong, Robert G., Cuccaro, Michael L., Pericak-Vance, Margaret A.

“…Autistic disorder (AutD) is a neurodevelopmental disorder characterized by significant impairment in social, communicative, and behavioral functioning. A…”
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An Analysis Paradigm for Investigating Multi‐locus Effects in Complex Disease: Examination of Three GABAA Receptor Subunit Genes on 15q11‐q13 as Risk Factors for Autistic Disorder by Ashley‐Koch, A. E., Mei, H., Jaworski, J., Ma, D. Q., Ritchie, M. D., Menold, M. M., Delong, G. R., Abramson, R. K., Wright, H. H., Hussman, J. P., Cuccaro, M. L., Gilbert, J. R., Martin, E. R., Pericak‐Vance, M. A.

“…Summary Gene‐gene interactions are likely involved in many complex genetic disorders and new statistical approaches for detecting such interactions are needed…”
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Genetic Studies of Autistic Disorder and Chromosome 7 by Ashley-Koch, A., Wolpert, C.M., Menold, M.M., Zaeem, L., Basu, S., Donnelly, S.L., Ravan, S.A., Powell, C.M., Qumsiyeh, M.B., Aylsworth, A.S., Vance, J.M., Gilbert, J.R., Wright, H.H., Abramson, R.K., DeLong, G.R., Cuccaro, M.L., Pericak-Vance, M.A.

“…Genome-wide scans have suggested that a locus on 7q is involved in the etiology of autistic disorder (AD). We have identified an AD family in which three sibs…”
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A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex by Haines, J.L, Ter-Minassian, M, Bazyk, A, Gusella, J.F, Kim, D.J, Terwedow, H, PericakVance, M.A, Rimmler, J.B, Haynes, C.S, Roses, A.D, Lee, A, Shaner, B, Menold, M, Seboun, E, Fitoussi, R-P, Gartioux, C, Reyes, C, Ribierre, F, Gyapay, G, Weissenbach, J, Hauser, S.L, Goodkin, D.E, Lincoln, R, Usuku, K, Garcia-Merino, A, Gatto, N, Young, S, Oksenberg, J.R

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Analysis of linkage disequilibrium in γ-aminobutyric acid receptor subunit genes in autistic disorder by Martin, E.R., Menold, M.M., Wolpert, C.M., Bass, M.P., Donnelly, S.L., Ravan, S.A., Zimmerman, A., Gilbert, J.R., Vance, J.M., Maddox, L.O., Wright, H.H., Abramson, R.K., DeLong, G.R., Cuccaro, M.L., Pericak-Vance, M.A.

“…Autistic disorder (AD) is a neurodevelopmental disorder characterized by abnormalities in behavior, communication, and social interactions and functioning…”
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Multiple susceptibility loci for multiple sclerosis by Haines, Jonathan L., Bradford, Yuki, Garcia, Melissa E., Reed, Allison D., Neumeister, Elizabeth, Pericak-Vance, Margaret A., Rimmler, Jacqueline B., Menold, Marissa M., Martin, Eden R., Oksenberg, Jorge R., Barcellos, Lisa F., Lincoln, Robin, Hauser, Stephen L.

“…Multiple sclerosis (MS) is a common and frequently disabling autoimmune disorder mediated by autoaggressive T cells and autoantibodies that target central…”
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Casein kinase I-like protein kinases encoded by YCK1 and YCK2 are required for yeast morphogenesis by ROBINSON, L. C, MENOLD, M. M, GARRETT, S, CULBERTSON, M. R

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An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder by Ashley-Koch, A E, Mei, H, Jaworski, J, Ma, D Q, Ritchie, M D, Menold, M M, Delong, G R, Abramson, R K, Wright, H H, Hussman, J P, Cuccaro, M L, Gilbert, J R, Martin, E R, Pericak-Vance, M A

“…Gene-gene interactions are likely involved in many complex genetic disorders and new statistical approaches for detecting such interactions are needed. We…”
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The Saccharomyces cerevisiae YAK1 gene encodes a protein kinase that is induced by arrest early in the cell cycle by GARRETT, S, MENOLD, M. M, BROACH, J. R

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Genetic studies in autistic disorder and chromosome 15 by BASS, M. P, MENOLD, M. M, GILBERT, J. R, CUCCARO, M. L, DELONG, G. R, PERICAK-VANCE, M. A, WOLPERT, C. M, DONNELLY, S. L, RAVAN, S. A, HAUSER, E. R, MADDOX, L. O, VANCE, J. M, ABRAMSON, R. K, WRIGHT, H. H

“…Autistic disorder (AD) is a developmental disorder affecting social interactions, communication, and behavior. AD is a disease of complex genetic architecture…”
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Ordered-subset analysis of savant skills in autism for 15q11-q13 by Ma, D.Q., Jaworski, J., Menold, M.M., Donnelly, S., Abramson, R.K., Wright, H.H., Delong, G.R., Gilbert, J.R., Pericak-Vance, M.A., Cuccaro, Michael L.

“…Autism is a complex disorder characterized by genetic and phenotypic heterogeneity. Analysis of phenotypically homogeneous subtypes has been used to both…”
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Three probands with autistic disorder and isodicentric chromosome 15 by Wolpert, Chantelle M., Menold, Marisa M., Bass, Meredyth P., Qumsiyeh, Mazin B., Donnelly, Shannon L., Ravan, Sarah A., Vance, Jeffery M., Gilbert, John R., Abramson, Ruth K., Wright, Harry H., Cuccaro, Michael L., Pericak-Vance, Margaret A.

“…We have identified three unrelated probands with autistic disorder (AD) and isodicentric chromosomes that encompass the proximal region of 15q11.2. All three…”
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Chapter 1 Focal Adhesions: New Angles on an Old Structure by Dubash, Adi D., Menold, Marisa M., Samson, Thomas, Boulter, Etienne, García-Mata, Rafael, Doughman, Renee, Burridge, Keith

“…Focal adhesions have been intensely studied ever since their discovery in 1971. The last three decades have seen major advances in understanding the structure…”
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Autistic Disorder and Chromosome 15q11–q13: Construction and Analysis of a BAC/PAC Contig by Maddox, Lewis O., Menold, Marisa M., Bass, Meredyth P., Rogala, Allison R., Pericak-Vance, Margaret A., Vance, Jeffery M., Gilbert, John R.

“…Autistic disorder (AD) is a neurodevelopmental disorder that affects approximately 2–10/10,000 individuals. Chromosome 15q11–q13 has been implicated in the…”
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Female with autistic disorder and monosomy X (Turner syndrome): Parent-of-origin effect of the X chromosome by Donnelly, Shannon L., Wolpert, Chantelle M., Menold, Marisa M., Bass, Meredyth P., Gilbert, John R., Cuccaro, Michael L., Delong, G. Robert, Pericak-Vance, Margaret A.

“…We have ascertained and examined a patient with autistic disorder (AD) and monosomy X (Turner syndrome). The patient met Diagnostic and Statistical Manual of…”
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No association between the APOE gene and autism by Raiford, K.L., Shao, Y., Allen, I.C., Martin, E.R., Menold, M.M., Wright, H.H., Abramson, R.K., Worley, G., DeLong, G.R., Vance, J.M., Cuccaro, M.L., Gilbert, J.R., Pericak-Vance, M.A.

“…Autism is a neurodevelopmental disorder characterized by stereotypic and repetitive behavior and interests, together with social and communicative…”
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Complete Genomic Screen in Late-Onset Familial Alzheimer’s Disease by Pericak-Vance, M.A, Bass, M.L, Yamaoka, L.H, Gaskell, P.C, Scott, W.K, Terwedow, H.A, Menold, M.M, Conneally, P.M, Small, G.W, Saunders, A.M, Roses, A.D, Haines, J.L

“…Alzheimer’s disease (AD) is a complex genetic disorder. Linkage analysis has helped unravel a portion of the genetic component of AD by identifying four loci…”
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