Search Results - "FLODMAN, P"

The Genetic Architecture of Selection at the Human Dopamine Receptor D4 ( DRD4) Gene Locus by Wang, E., Ding, Y.-C., Flodman, P., Kidd, J.R., Kidd, K.K., Grady, D.L., Ryder, O.A., Spence, M.A., Swanson, J.M., Moyzis, R.K.

“…Associations of the seven-repeat (7R) allele of the human dopamine receptor D4 ( DRD4) gene with both the personality trait of novelty seeking and attention…”
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Evidence for multiple loci from a genome scan of autism kindreds by SCHELLENBERG, G. D, DAWSON, G, LEONG, L, YU, C.-E, STODGELL, C, RODIER, P. M, SPENCE, M. A, MINSHEW, N, MCMAHON, W. M, WIJSMAN, E. M, SUNG, Y. J, ESTES, A, MUNSON, J, ROSENTHAL, E, ROTHSTEIN, J, FLODMAN, P, SMITH, M, COON, H

“…We performed a genome-wide linkage scan using highly polymorphic microsatellite markers. To minimize genetic heterogeneity, we focused on sibpairs meeting the…”
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High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder by GRADY, D. L, CHI, H-C, DING, Y-C, SMITH, M, WANG, E, SCHUCK, S, FLODMAN, P, SPENCE, M. A, SWANSON, J. M, MOYZIS, R. K

“…Associations have been reported of the 7-repeat (7R) allele of the human dopamine receptor D4 (DRD4) gene with both the personality trait of novelty seeking…”
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Sequence variants of the DRD4 gene in autism: Further evidence that rare DRD4 7R haplotypes are ADHD specific by Grady, D.L., Harxhi, A., Smith, M., Flodman, P., Spence, M.A., Swanson, J.M., Moyzis, R.K.

“…A high prevalence of rare dopamine receptor D4 (DRD4) alleles in children diagnosed with attention‐deficit hyperactivity disorder (ADHD) has been reported…”
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A new βA1-crystallin splice junction mutation in autosomal dominant cataract by BATEMAN, J. Bronwyn, GEYER, David D, FLODMAN, Pamela, JOHANNES, Meriam, SIKELA, James, WALTER, Nicole, MOREIRA, Ana Teresa, CLANCY, Kevin, SPENCE, M. Anne

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Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease by Kandt, R. S, Haines, J. L, Smith, M, Northrup, H, Gardner, R. J. M, Short, M. P, Dumars, K, Roach, E. S, Steingold, S, Wall, S, Blanton, S. H, Flodman, P, Kwiatkowski, D. J, Jewell, A, Weber, J. L, Roses, A. D, Pericak-Vance, M. A

“…Tuberous sclerosis complex (TSC) is an autosomal dominant disorder of unknown aetiology that affects numerous body systems including skin, brain and kidneys…”
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A genetic linkage map of the rat derived from recombinant inbred strains by Pravenec, M, Gauguier, D, Schott, J J, Buard, J, Kren, V, Bílá, V, Szpirer, C, Szpirer, J, Wang, J M, Huang, H, St Lezin, E, Spence, M A, Flodman, P, Printz, M, Lathrop, G M, Vergnaud, G, Kurtz, T W

“…We have constructed a genetic linkage map in the rat by analyzing the strain distribution patterns of 500 genetic markers in a large set of recombinant inbred…”
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Evidence for genetic linkage of autism to chromosomes 7 and 4 by Schellenberg, G D, Dawson, G, Sung, Y J, Estes, A, Munson, J, Rosenthal, E, Rothstein, J, Flodman, P, Smith, M, Coon, H, Leong, L, C-E, Yu, Stodgell, C, Rodier, P M, Spence, M A, Minshew, N, McMahon, W M, Wijsman, E M

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Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficits by Smith, M, Woodroffe, A, Smith, R, Holguin, S, Martinez, J, Filipek, P A, Modahl, C, Moore, B, Bocian, M E, Mays, L, Laulhere, T, Flodman, P, Spence, M A

“…In a sporadic case of autism and language deficit due to auditory processing defects, molecular genetic studies revealed that a chromosomal deletion occurred…”
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Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR by Smith, M, Escamilla, J R, Filipek, P, Bocian, M E, Modahl, C, Flodman, P, Spence, M A

“…We recently studied a patient who meets criteria for autistic disorder and has a 2q37 deletion. Molecular cytogenetic studies were carried out using DNA…”
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Analysis of financial barriers experienced by prospective genetic counseling students by Lee, Dexter, Platt, Julia, Flodman, Pamela L., Singh, Kathryn E., Quintero-Rivera, Fabiola

“…High costs of applying to genetic counseling graduate programs (GCGPs) are likely a barrier to workforce diversification. We sought to determine application…”
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Bipolar disorder: evidence for a major locus by Spence, M A, Flodman, P L, Sadovnick, A D, Bailey-Wilson, J E, Ameli, H, Remick, R A

“…Complex segregation analyses were conducted on families of bipolar I and bipolar II probands to delineate the mode of inheritance. The probands were…”
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Preliminary Implementation of New Data Mining Techniques for the Analysis of Simulation Data from Genetic Analysis Workshop 12: Problem 2 by Flodman, Pamela, Macula, Anthony J., Spence, M. Anne, Torney, David C.

“…We introduce a new data mining method applicable to complex disease genetics. Our approach is suited to a broad spectrum of diseases, identifying the…”
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Co-occurrence of celiac disease and other autoimmune diseases in celiacs and their first-degree relatives by Neuhausen, Susan L, Steele, Linda, Ryan, Sarah, Mousavi, Maryam, Pinto, Marie, Osann, Kathryn E, Flodman, Pamela, Zone, John J

“…Abstract The occurrence of other autoimmune diseases in celiac disease families has not been previously reported in a North American population. We…”
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Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa by KOJIS, T. L, HEINZMANN, C, FLODMAN, P, NGO, J. T, SPARKES, R. S, SPENCE, M. A, BATEMAN, J. B, HECKENLIVELY, J. R

“…In order to elucidate the genetic basis of autosomal dominant retinitis pigmentosa (adRP) in a large eight-generation family (UCLA-RP09) of British descent, we…”
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Evidence of Positive Selection Acting at the Human Dopamine Receptor D4 Gene Locus by Ding, Yuan-Chun, Chi, Han-Chang, Grady, Deborah L., Morishima, Atsuyuki, Kidd, Judith R., Kidd, Kenneth K., Flodman, Pamela, Spence, M. Anne, Schuck, Sabrina, Swanson, James M., Zhang, Ya-Ping, Moyzis, Robert K.

“…Associations have been reported of the seven-repeat (7R) allele of the human dopamine receptor D4 (DRD4) gene with both attention-deficit/hyperactivity…”
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Estimating recombination fraction separately for males and females: a counterintuitive result by Hodge, S E, Flodman, P L, Duryea, M F, Spence, M A

“…In the course of performing a linkage analysis on rats bred from inbred doubly heterozygous parents, we observed the following counterintuitive finding: the…”
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Dopamine genes and ADHD by Swanson, J.M, Flodman, Pamela, Kennedy, James, Spence, M.Anne, Moyzis, Robert, Schuck, Sabrina, Murias, Michael, Moriarity, Joan, Barr, Cathy, Smith, Moyra, Posner, Michael

“…Family, twin, and adoption studies have documented a strong genetic basis for ADHD/HKD, but these studies do not identify specific genes linked to the…”
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Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigrees by Munier, F L, Arabien, L, Flodman, P, Spence, M A, Pescia, G, Rutz, H P, Murphree, A L

“…In a previous genotypic study of eight families, we described paternal segregation distortion favoring the transmission of mutant alleles at the retinoblastoma…”
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Language and other regression: Assessment and timing by GOLDBERG, Wendy A, OSANN, Kathy, FILIPEK, Pauline A, LAULHERE, Tracy, JARVIS, Kelly, MODAHL, Charlotte, FLODMAN, Pamela, SPENCE, M. Anne

“…Understanding of regression in autism has been hampered by variability in parental and clinical recognition and reporting of lost skills. This study introduced…”
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