DRD2 and PPP1R1B (DARPP-32) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in male-only affected sib-pair families
Hettinger, Joe A, Liu, Xudong, Hudson, Melissa L, Lee, Alana, Cohen, Ira L, Michaelis, Ron C, Schwartz, Charles E, Lewis, Suzanne M E, Holden, Jeanette J A
Published in Behavioral and brain functions (04.05.2012)
Published in Behavioral and brain functions (04.05.2012)
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Journal Article
SALL1 mutation analysis in Townes-Brocks syndrome: twelve novel mutations and expansion of the phenotype
Botzenhart, Elke M., Green, Andrew, Ilyina, Helena, König, Rainer, Lowry, R. Brian, Lo, Ivan F. M., Shohat, Mordechai, Burke, Leah, McGaughran, Julie, Chafai, Ronit, Pierquin, Geneviève, Michaelis, Ron C, Whiteford, Margo L., Simola, Kalle O. J., Rösler, Bernd, Kohlhase, Jürgen
Published in Human mutation (01.09.2005)
Published in Human mutation (01.09.2005)
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Journal Article
Linkage Disequilibrium at the Angelman Syndrome Gene UBE3A in Autism Families
Nurmi, Erika L., Bradford, Yuki, Chen, Yi-hui, Hall, Jenifer, Arnone, Brenda, Gardiner, Mary Beth, Hutcheson, Holli B., Gilbert, John R., Pericak-Vance, Margaret A., Copeland-Yates, Susan A., Michaelis, Ron C., Wassink, Thomas H., Santangelo, Susan L., Sheffield, Val C., Piven, Joseph, Folstein, Susan E., Haines, Jonathan L., Sutcliffe, James S.
Published in Genomics (San Diego, Calif.) (01.09.2001)
Published in Genomics (San Diego, Calif.) (01.09.2001)
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Journal Article
A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families
Hettinger, Joe A., Liu, Xudong, Schwartz, Charles E., Michaelis, Ron C., Holden, Jeanette J.A.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.07.2008)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.07.2008)
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Journal Article
A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A
Jiang, Yong-hui, Sahoo, Trilochan, Michaelis, Ron C., Bercovich, Dani, Bressler, Jan, Kashork, Catherine D., Liu, Qian, Shaffer, Lisa G., Schroer, Richard J., Stockton, David W., Spielman, Richard S., Stevenson, Roger E., Beaudet, Arthur L.
Published in American journal of medical genetics. Part A (15.11.2004)
Published in American journal of medical genetics. Part A (15.11.2004)
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Journal Article
Absence of MeCP2 mutations in patients from the South Carolina autism project
Lobo-Menendez, Fe, Sossey-Alaoui, Khalid, Bell, Jennifer M., Copeland-Yates, Susan A., Plank, Sara M., Sanford, Stewart O., Skinner, Cindy, Simensen, Richard J., Schroer, Richard J., Michaelis, Ron C.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (15.02.2003)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (15.02.2003)
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Journal Article
Familial pericentric inversion of chromosome 18: behavioral abnormalities in patients heterozygous for either the dup(18p) del(18q) or dup(18q) del(18p) recombinant chromosome
VERMEULEN, Stefan J, SPELEMAN, Frank, VANRANSBEECK, Leen, VERSPEET, Jasmien, MENTEN, Björn, VERSCHRAEGEN-SPAE, Marie-Rose, DE WILDE, Philippe, MESSIAEN, Ludwine, MICHAELIS, Ron C, LEROY, Jules G
Published in European journal of human genetics : EJHG (01.01.2005)
Published in European journal of human genetics : EJHG (01.01.2005)
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Journal Article
The HOXA1 A218G polymorphism and autism: Lack of association in white and black patients from the South Carolina Autism Project
COLLINS, Julianne S, SCHROER, Richard J, BIRD, Jeffrey, MICHAELIS, Ron C
Published in Journal of autism and developmental disorders (01.06.2003)
Published in Journal of autism and developmental disorders (01.06.2003)
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Journal Article
Microsatellite analysis reveals a high incidence of maternal cell contamination in 46,XX products of conception consisting of villi or a combination of villi and membranous material
Jarrett, Kristine L., Michaelis, Ron C., Phelan, Mary C., Vincent, Victoria A., Best, Robert G.
Published in American journal of obstetrics and gynecology (01.07.2001)
Published in American journal of obstetrics and gynecology (01.07.2001)
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Journal Article
Hydrocephalus and intestinal aganglionosis: is L1CAM a modifier gene in Hirschsprung disease?
Parisi, Melissa A, Kapur, Raj P, Neilson, Ian, Hofstra, Robert M W, Holloway, Lynda W, Michaelis, Ron C, Leppig, Kathleen A
Published in American journal of medical genetics (15.02.2002)
Published in American journal of medical genetics (15.02.2002)
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Journal Article
Prenatal Diagnosis of L1 Cell Adhesion Molecule Mutations
Moya, Graciela E., Michaelis, Ron C., Holloway, Lynda W., Sanchez, Jose Maria
Published in Fetal diagnosis and therapy (2002)
Published in Fetal diagnosis and therapy (2002)
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Journal Article
Prenatal diagnosis of mosaicism for triploidy and trisomy 13
Phelan, Mary C., Curtis Rogers, R., Michaelis, Ron C., Lynn Moore, C., Blackburn, Will
Published in Prenatal diagnosis (01.06.2001)
Published in Prenatal diagnosis (01.06.2001)
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Journal Article
The HOPA Gene Dodecamer Duplication Is Not a Significant Etiological Factor in Autism
Michaelis, Ron C, Copeland-Yates, Susan A, Sossey-Alaoui, Khalid, Skinner, Cindy, Friez, Michael J, Longshore, John W, Simensen, Richard J, Schroer, Richard J, Stevenson, Roger E
Published in Journal of autism and developmental disorders (01.08.2000)
Published in Journal of autism and developmental disorders (01.08.2000)
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Journal Article
Molecular cytogenetic characterization of a de novo unbalanced translocation leading to trisomy 17q25-->qter and monosomy 18p11.3-->pter in a girl with dysmorphic features
Velagaleti, Gopalrao V N, Jalal, Syed M, Michaelis, Ron C, Rowe, Thomas F, Nichols, Jerilynn R, Lockhart, Lillian H
Published in Clinical dysmorphology (01.01.2003)
Published in Clinical dysmorphology (01.01.2003)
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Journal Article
Autism and maternally derived aberrations of chromosome 15q
Schroer, R J, Phelan, M C, Michaelis, R C, Crawford, E C, Skinner, S A, Cuccaro, M, Simensen, R J, Bishop, J, Skinner, C, Fender, D, Stevenson, R E
Published in American journal of medical genetics (01.04.1998)
Published in American journal of medical genetics (01.04.1998)
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Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autism
Plank, S M, Copeland-Yates, S A, Sossey-Alaoui, K, Bell, J M, Schroer, R J, Skinner, C, Michaelis, R C
Published in American journal of medical genetics (08.07.2001)
Published in American journal of medical genetics (08.07.2001)
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Journal Article
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 in a boy with a balanced 3;21 translocation
Bassett, L L, Michaelis, R C, Geiger, M H, Tarleton, J, Moore, C L, Knops, J F, Carroll, A J, Proud, V K
Published in American journal of medical genetics (15.04.2001)
Published in American journal of medical genetics (15.04.2001)
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