These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 38216835)

  • 1. Behavioral Phenotypes and Comorbidity in 3q29 Deletion Syndrome: Results from the 3q29 Registry.
    Pollak RM; Mortillo M; Murphy MM; Mulle JG
    J Autism Dev Disord; 2024 Jan; ():. PubMed ID: 38216835
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry.
    Pollak RM; Murphy MM; Epstein MP; Zwick ME; Klaiman C; Saulnier CA; ; Mulle JG
    Mol Autism; 2019; 10():30. PubMed ID: 31346402
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autism spectrum disorder symptom expression in individuals with 3q29 deletion syndrome.
    Pollak RM; Pincus JE; Burrell TL; Cubells JF; Klaiman C; Murphy MM; Saulnier CA; Walker EF; White SP; Mulle JG
    Mol Autism; 2022 Dec; 13(1):50. PubMed ID: 36566217
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Musculoskeletal phenotypes in 3q29 deletion syndrome.
    Pollak RM; Tilmon JC; Murphy MM; Gambello MJ; Russo RS; Dormans JP; Mulle JG
    medRxiv; 2023 Apr; ():. PubMed ID: 37066183
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Musculoskeletal phenotypes in 3q29 deletion syndrome.
    Pollak RM; Tilmon JC; Murphy MM; Gambello MJ; Sanchez Russo R; Dormans JP; Mulle JG
    Am J Med Genet A; 2023 Nov; 191(11):2749-2756. PubMed ID: 37691301
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Visual-Motor Integration Deficits in 3q29 Deletion Syndrome.
    Pollak RM; Burrell TL; Cubells JF; Klaiman C; Murphy MM; Saulnier CA; Walker EF; White SP; Mulle JG
    J Autism Dev Disord; 2024 Aug; 54(8):3142-3154. PubMed ID: 37354284
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Adaptive behaviour deficits in individuals with 3q29 deletion syndrome.
    Pollak RM; Burrell TL; Cubells JF; Klaiman C; Murphy MM; Saulnier CA; Walker EF; White SP; Mulle JG
    J Intellect Disabil Res; 2024 Feb; 68(2):113-127. PubMed ID: 37740553
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Adaptive behavior deficits in individuals with 3q29 deletion syndrome.
    Pollak RM; Burrell TL; Cubells JF; Klaiman C; Murphy MM; Saulnier CA; Walker EF; White SP; Mulle JG
    medRxiv; 2023 Apr; ():. PubMed ID: 37066139
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Study protocol for The Emory 3q29 Project: evaluation of neurodevelopmental, psychiatric, and medical symptoms in 3q29 deletion syndrome.
    Murphy MM; Lindsey Burrell T; Cubells JF; España RA; Gambello MJ; Goines KCB; Klaiman C; Li L; Novacek DM; Papetti A; Sanchez Russo RL; Saulnier CA; Shultz S; Walker E; Mulle JG
    BMC Psychiatry; 2018 Jun; 18(1):183. PubMed ID: 29884173
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Craniofacial features of 3q29 deletion syndrome: Application of next-generation phenotyping technology.
    Mak BC; Sanchez Russo R; Gambello MJ; Fleischer N; Black ED; Leslie E; Murphy MM; ; Mulle JG
    Am J Med Genet A; 2021 Jul; 185(7):2094-2101. PubMed ID: 33938623
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Symptoms of Pediatric Feeding Disorders Among Individuals with 3q29 Deletion Syndrome: A Case-Control Study.
    Wawrzonek AJ; Sharp W; Burrell TL; Gillespie SE; Pollak RM; Murphy MM; Mulle JG;
    J Dev Behav Pediatr; 2022 Apr; 43(3):e170-e178. PubMed ID: 34636361
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel features of 3q29 deletion syndrome: Results from the 3q29 registry.
    Glassford MR; Rosenfeld JA; Freedman AA; Zwick ME; Mulle JG;
    Am J Med Genet A; 2016 Apr; 170A(4):999-1006. PubMed ID: 26738761
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Convergent and distributed effects of the 3q29 deletion on the human neural transcriptome.
    Sefik E; Purcell RH; ; Walker EF; Bassell GJ; Mulle JG
    Transl Psychiatry; 2021 Jun; 11(1):357. PubMed ID: 34131099
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comprehensive phenotyping of neuropsychiatric traits in a multiplex 3q29 deletion family: a case report.
    Murphy MM; Burrell TL; Cubells JF; Epstein MT; Espana R; Gambello MJ; Goines K; Klaiman C; Koh S; Russo RS; Saulnier CA; Walker E; ; Mulle JG
    BMC Psychiatry; 2020 Apr; 20(1):184. PubMed ID: 32321479
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evaluation of psychiatric comorbidity in attention-deficit hyperactivity disorder with epilepsy: A case-control study.
    Ahmed GK; Darwish AM; Khalifa H; Khashbah MA
    Epilepsy Res; 2021 Jan; 169():106505. PubMed ID: 33302225
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A potential electroencephalography and cognitive biosignature for the child behavior checklist-dysregulation profile.
    McGough JJ; McCracken JT; Cho AL; Castelo E; Sturm A; Cowen J; Piacentini J; Loo SK
    J Am Acad Child Adolesc Psychiatry; 2013 Nov; 52(11):1173-82. PubMed ID: 24157391
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Psychosis spectrum symptoms among individuals with schizophrenia-associated copy number variants and evidence of cerebellar correlates of symptom severity.
    Sefik E; Guest RM; Aberizk K; Espana R; Goines K; Novacek DM; Murphy MM; Goldman-Yassen AE; Cubells JF; Ousley O; Li L; Shultz S; Walker EF; Mulle JG
    Psychiatry Res; 2024 May; 335():115867. PubMed ID: 38537595
    [TBL] [Abstract][Full Text] [Related]  

  • 18. New phenotypes associated with 3q29 duplication syndrome: Results from the 3q29 registry.
    Pollak RM; Zinsmeister MC; Murphy MM; Zwick ME; ; Mulle JG
    Am J Med Genet A; 2020 May; 182(5):1152-1166. PubMed ID: 32154651
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Emotional and Behavioral Problems in 4- and 5-Year Old Children With and Without Motor Delays.
    Rodriguez MC; Wade TJ; Veldhuizen S; Missiuna C; Timmons B; Cairney J
    Front Pediatr; 2019; 7():474. PubMed ID: 31803697
    [No Abstract]   [Full Text] [Related]  

  • 20. Cross-species transcriptomic analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion.
    Purcell RH; Sefik E; Werner E; King AT; Mosley TJ; Merritt-Garza ME; Chopra P; McEachin ZT; Karne S; Raj N; Vaglio BJ; Sullivan D; Firestein BL; Tilahun K; Robinette MI; Warren ST; Wen Z; Faundez V; Sloan SA; Bassell GJ; Mulle JG
    bioRxiv; 2023 May; ():. PubMed ID: 36747819
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.