BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 36475376)

  • 1. Prevalence and Penetrance of Rare Pathogenic Variants in Neurodevelopmental Psychiatric Genes in a Health Care System Population.
    Shimelis H; Oetjens MT; Walsh LK; Wain KE; Znidarsic M; Myers SM; Finucane BM; Ledbetter DH; Martin CL
    Am J Psychiatry; 2023 Jan; 180(1):65-72. PubMed ID: 36475376
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population.
    Martin CL; Wain KE; Oetjens MT; Tolwinski K; Palen E; Hare-Harris A; Habegger L; Maxwell EK; Reid JG; Walsh LK; Myers SM; Ledbetter DH
    JAMA Psychiatry; 2020 Dec; 77(12):1276-1285. PubMed ID: 32697297
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Medical manifestations and health care utilization among adult MyCode participants with neurodevelopmental psychiatric copy number variants.
    Finucane B; Oetjens MT; Johns A; Myers SM; Fisher C; Habegger L; Maxwell EK; Reid JG; Ledbetter DH; Kirchner HL; Martin CL
    Genet Med; 2022 Mar; 24(3):703-711. PubMed ID: 34906480
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Subcortical Brain Alterations in Carriers of Genomic Copy Number Variants.
    Kumar K; Modenato C; Moreau C; Ching CRK; Harvey A; Martin-Brevet S; Huguet G; Jean-Louis M; Douard E; Martin CO; Younis N; Tamer P; Maillard AM; Rodriguez-Herreros B; Pain A; ; Kushan L; Isaev D; Alpert K; Ragothaman A; Turner JA; Wang L; Ho TC; Schmaal L; Silva AI; van den Bree MBM; Linden DEJ; Owen MJ; Hall J; Lippé S; Dumas G; Draganski B; Gutman BA; Sønderby IE; Andreassen OA; Schultz LM; Almasy L; Glahn DC; Bearden CE; Thompson PM; Jacquemont S
    Am J Psychiatry; 2023 Sep; 180(9):685-698. PubMed ID: 37434504
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders.
    Calle Sánchez X; Helenius D; Bybjerg-Grauholm J; Pedersen C; Hougaard DM; Børglum AD; Nordentoft M; Mors O; Mortensen PB; Geschwind DH; Montalbano S; Raznahan A; Thompson WK; Ingason A; Werge T
    JAMA Psychiatry; 2022 Jan; 79(1):59-69. PubMed ID: 34817560
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Population Genomic Screening for Genetic Etiologies of Neurodevelopmental/Psychiatric Disorders Demonstrates Personal Utility and Positive Participant Responses.
    Wain KE; Tolwinski K; Palen E; Heidlebaugh AR; Holdren K; Walsh LK; Oetjens MT; Ledbetter DH; Martin CL
    J Pers Med; 2021 May; 11(5):. PubMed ID: 34062946
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical Characterization of Copy Number Variants Associated With Neurodevelopmental Disorders in a Large-scale Multiancestry Biobank.
    Birnbaum R; Mahjani B; Loos RJF; Sharp AJ
    JAMA Psychiatry; 2022 Mar; 79(3):250-259. PubMed ID: 35080590
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia.
    Lowther C; Merico D; Costain G; Waserman J; Boyd K; Noor A; Speevak M; Stavropoulos DJ; Wei J; Lionel AC; Marshall CR; Scherer SW; Bassett AS
    Genome Med; 2017 Nov; 9(1):105. PubMed ID: 29187259
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association of Rare Copy Number Variants With Risk of Depression.
    Kendall KM; Rees E; Bracher-Smith M; Legge S; Riglin L; Zammit S; O'Donovan MC; Owen MJ; Jones I; Kirov G; Walters JTR
    JAMA Psychiatry; 2019 Aug; 76(8):818-825. PubMed ID: 30994872
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays.
    Costain G; Lionel AC; Merico D; Forsythe P; Russell K; Lowther C; Yuen T; Husted J; Stavropoulos DJ; Speevak M; Chow EW; Marshall CR; Scherer SW; Bassett AS
    Hum Mol Genet; 2013 Nov; 22(22):4485-501. PubMed ID: 23813976
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Increased Prevalence of Rare Copy Number Variants in Treatment-Resistant Psychosis.
    Farrell M; Dietterich TE; Harner MK; Bruno LM; Filmyer DM; Shaughnessy RA; Lichtenstein ML; Britt AM; Biondi TF; Crowley JJ; Lázaro-Muñoz G; Forsingdal AE; Nielsen J; Didriksen M; Berg JS; Wen J; Szatkiewicz J; Mary Xavier R; Sullivan PF; Josiassen RC
    Schizophr Bull; 2023 Jul; 49(4):881-892. PubMed ID: 36454006
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Copy number variations and cognitive phenotypes in unselected populations.
    Männik K; Mägi R; Macé A; Cole B; Guyatt AL; Shihab HA; Maillard AM; Alavere H; Kolk A; Reigo A; Mihailov E; Leitsalu L; Ferreira AM; Nõukas M; Teumer A; Salvi E; Cusi D; McGue M; Iacono WG; Gaunt TR; Beckmann JS; Jacquemont S; Kutalik Z; Pankratz N; Timpson N; Metspalu A; Reymond A
    JAMA; 2015 May; 313(20):2044-54. PubMed ID: 26010633
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders.
    Thygesen JH; Wolfe K; McQuillin A; Viñas-Jornet M; Baena N; Brison N; D'Haenens G; Esteba-Castillo S; Gabau E; Ribas-Vidal N; Ruiz A; Vermeesch J; Weyts E; Novell R; Buggenhout GV; Strydom A; Bass N; Guitart M; Vogels A
    Br J Psychiatry; 2018 May; 212(5):287-294. PubMed ID: 29693535
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Penetrance for copy number variants associated with schizophrenia.
    Vassos E; Collier DA; Holden S; Patch C; Rujescu D; St Clair D; Lewis CM
    Hum Mol Genet; 2010 Sep; 19(17):3477-81. PubMed ID: 20587603
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia.
    Mojarad BA; Yin Y; Manshaei R; Backstrom I; Costain G; Heung T; Merico D; Marshall CR; Bassett AS; Yuen RKC
    Transl Psychiatry; 2021 Feb; 11(1):84. PubMed ID: 33526774
    [TBL] [Abstract][Full Text] [Related]  

  • 16. All for one and one for all: heterogeneity of genetic etiologies in neurodevelopmental psychiatric disorders.
    Moreno-De-Luca D; Martin CL
    Curr Opin Genet Dev; 2021 Jun; 68():71-78. PubMed ID: 33773394
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The penetrance of copy number variations for schizophrenia and developmental delay.
    Kirov G; Rees E; Walters JT; Escott-Price V; Georgieva L; Richards AL; Chambert KD; Davies G; Legge SE; Moran JL; McCarroll SA; O'Donovan MC; Owen MJ
    Biol Psychiatry; 2014 Mar; 75(5):378-85. PubMed ID: 23992924
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The contribution of copy number variants to psychiatric symptoms and cognitive ability.
    Mollon J; Almasy L; Jacquemont S; Glahn DC
    Mol Psychiatry; 2023 Apr; 28(4):1480-1493. PubMed ID: 36737482
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia.
    Rees E; Kendall K; Pardiñas AF; Legge SE; Pocklington A; Escott-Price V; MacCabe JH; Collier DA; Holmans P; O'Donovan MC; Owen MJ; Walters JTR; Kirov G
    JAMA Psychiatry; 2016 Sep; 73(9):963-969. PubMed ID: 27602560
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Reduced burden of very large and rare CNVs in bipolar affective disorder.
    Grozeva D; Kirov G; Conrad DF; Barnes CP; Hurles M; Owen MJ; O'Donovan MC; Craddock N
    Bipolar Disord; 2013 Dec; 15(8):893-8. PubMed ID: 24127788
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.