Search Results - "Ivankovic, Franjo"

Loss of MBNL1 induces RNA misprocessing in the thymus and peripheral blood by Sznajder, Łukasz J., Scotti, Marina M., Shin, Jihae, Taylor, Katarzyna, Ivankovic, Franjo, Nutter, Curtis A., Aslam, Faaiq N., Subramony, S. H., Ranum, Laura P. W., Swanson, Maurice S.

“…The thymus is a primary lymphoid organ that plays an essential role in T lymphocyte maturation and selection during development of one arm of the mammalian…”
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F64. GENOME-WIDE ANALYSES OF INATTENTION AND HYPERACTIVITY/IMPULSIVITY: BIOLOGICAL AND CLINICAL IMPLICATIONS FOR ATTENTION DEFICIT HYPERACTIVITY DISORDER by Ivankovic, Franjo

“…Attention deficit hyperactivity disorder (ADHD) is a common and highly heritable childhood onset psychiatric condition, with two main symptom domains:…”
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67. Optimization of Psychiatric Phenotypes for Genetic Studies by Ivankovic, Franjo, Mathews, Carol

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T87. COPY-NUMBER VARIATION IN TOURETTE SYNDROME FAMILIES, ANALYSIS OF DE NOVO AND INHERITED CNVS by Ivankovic, Franjo, Mathews, Carol

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GENETIC AND PHENOTYPIC ARCHITECTURE OF OCD IN ABCD STUDY by Ivankovic, Franjo, Johnson, Sharon, Mathews, Carol

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LEVERAGING MULTI-MODAL DATA FROM THE ABCD STUDY TO REFINE OCD PHENOTYPE FOR GENETIC ANALYSES by Ivankovic, Franjo, Singh, Aryan, Kumar, Shashank, Gupta, Richa, Mathews, Carol

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TH54. GENETICS OF CHILDHOOD PSYCHIATRIC BURDEN AND OBSESSIVE-COMPULSIVE DISORDER by Ivankovic, Franjo, Johnson, Sharon, Shen, James, Mathews, Carol

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Optimization of self- or parent-reported psychiatric phenotypes in longitudinal studies by Ivankovic, Franjo, Johnson, Sharon, Shen, James, Scharf, Jeremiah M, Mathews, Carol A

“…The Adolescent Brain Cognitive Development (ABCD) study is a longitudinal study of US adolescents with a wide breadth of psychiatric, neuroimaging and genetic…”
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T59. MARKER MATCH: A PROXIMITY BASED PROBE-MATCHING ALGORITHM FOR JOINT ANALYSIS OF CNVS FROM DIFFERENT GENOTYPING ARRAYS AND SUBSEQUENT CNV ASSOCIATION STUDY OF TOURETTE SYNDROME by Ivankovic, Franjo, Yu, Dongmei, Domenech, Laura, Zhan, Lingyu, Ophoff, Roel, Scharf, Jeremiah, Mathews, Carol

“…Copy-number variants (CNVs) are structural mutations in the genome resulting from deletions or duplications of large segments of DNA and can affect a wide…”
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T24. UNCOVERING EATING DISORDER GENETICS THROUGH LARGE SCALE SEQUENCING by Ivankovic, Franjo, Javaras, Kristin N, Pennels, Kaitlin, Stevens, Christine, Stroud, Rocky, Jennings, Faith, Daly, Mark, Neale, Benjamin

“…Both anorexia (AN) and bulimia (BN) nervosa are marked by a substantial genetic component, with family study heritability estimates of 0.58-0.76 for AN and…”
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Genomics and Phenomics of Obsessive-Compulsive and Related Disorders by Ivankovic, Franjo

“…Tourette syndrome (TS) and obsessive-compulsive disorder (OCD) are neuropsychiatric disorders with onset in childhood affecting 0.6% and 2.3% of people,…”
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W50. LARGE-SCALE TOURETTE SYNDROME WHOLE-EXOME SEQUENCING ANALYSIS REVEALS A SIGNIFICANT CONTRIBUTION OF DE NOVO MUTATIONS DIFFERENT FROM AUTISM SPECTRUM DISORDER by Zhan, Lingyu, Yu, Dongmei, Domenech, Laura, Ivankovic, Franjo, Giusti-Rodriguez, Paola, Niarchou, Maria, Davis, Lea K., Mathews, Carol, Scharf, Jeremiah, Ophoff, Roel

“…Tourette syndrome (TS) is an early-onset neurodevelopmental disorder (NDD) characterized by vocal and motor tics. TS is highly heritable (60-80%) and has a…”
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T50. ANALYZING LARGE-SCALE TOURETTE SYNDROME WHOLE-EXOME SEQUENCING DATA REVEALS A SIGNIFICANT CONTRIBUTION OF DE NOVO MUTATIONS by Zhan, Lingyu, Yu, Dongmei, Domenech-Salgado, Laura, Ivankovic, Franjo, Giusti-Rodriguez, Paola, Niarchou, Maria, Davis, Lea K., Mathews, Carol A., Scharf, Jeremiah M., Ophoff, Roel A.

“…Tourette syndrome (TS) is an early-onset neurodevelopmental disorder (NDD) characterized by vocal and motor tics. TS is highly heritable (60-80%) and has a…”
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Cell-type-specific dysregulation of RNA alternative splicing in short tandem repeat mouse knockin models of myotonic dystrophy by Nutter, Curtis A, Bubenik, Jodi L, Oliveira, Ruan, Ivankovic, Franjo, Sznajder, Łukasz J, Kidd, Benjamin M, Pinto, Belinda S, Otero, Brittney A, Carter, Helmut A, Vitriol, Eric A, Wang, Eric T, Swanson, Maurice S

“…Short tandem repeats (STRs) are prone to expansion mutations that cause multiple hereditary neurological and neuromuscular diseases. To study pathomechanisms…”
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Is Persistent Motor or Vocal Tic Disorder a Milder Form of Tourette Syndrome? by Claudio‐Campos, Karla, Stevens, Daniel, Koo, Sang‐Wahn, Valko, Alexa, Bienvenu, Oscar Joseph, Budman, Cathy B., Cath, Danielle C., Darrow, Sabrina, Geller, Daniel, Goes, Fernando S., Grados, Marco A., Greenberg, Benjamin D., Greenberg, Erica, Hirschtritt, Matthew E., Illmann, Cornelia, Ivankovic, Franjo, King, Robert A., Knowles, James A., Krasnow, Janice, Lee, Paul C., Lyon, Gholson J., McCracken, James T., Robertson, Mary M., Osiecki, Lisa, Riddle, Mark A., Rouleau, Guy, Sandor, Paul, Nestadt, Gerald, Samuels, Jack, Scharf, Jeremiah M., Mathews, Carol A.

“…Background Persistent motor or vocal tic disorder (PMVT) has been hypothesized to be a forme fruste of Tourette syndrome (TS). Although the primary diagnostic…”
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T50. ANALYZING LARGE-SCALE TOURETTE SYNDROME WHOLE-EXOME SEQUENCING DATA REVEALS A SIGNIFICANT CONTRIBUTION OF DE NOVO MUTATIONS by Zhan, Lingyu, Yu, Dongmei, Domenech-Salgado, Laura, Ivankovic, Franjo, Giusti-Rodriguez, Paola, Niarchou, Maria, Davis, Lea K., Mathews, Carol A., Scharf, Jeremiah M., Ophoff, Roel A.

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SFMetaDB: a comprehensive annotation of mouse RNA splicing factor RNA-Seq datasets by Li, Jin, Tseng, Ching-San, Federico, Antonio, Ivankovic, Franjo, Huang, Yi-Shuian, Ciccodicola, Alfredo, Swanson, Maurice S, Yu, Peng

“…Although the number of RNA-Seq datasets deposited publicly has increased over the past few years, incomplete annotation of the associated metadata limits their…”
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RBPMetaDB: a comprehensive annotation of mouse RNA-Seq datasets with perturbations of RNA-binding proteins by Li, Jin, Deng, Su-Ping, Vieira, Jacob, Thomas, James, Costa, Valerio, Tseng, Ching-San, Ivankovic, Franjo, Ciccodicola, Alfredo, Yu, Peng

“…RNA-binding proteins (RBPs) may play a critical role in gene regulation in various diseases or biological processes by controlling post-transcriptional events…”
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