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 *

202 related articles for article (PubMed ID: 35312124)

  • 1. Whole-exome DNA sequencing in childhood anxiety disorders identifies rare de novo damaging coding variants.
    Olfson E; Lebowitz ER; Hommel G; Pashankar N; Silverman WK; Fernandez TV
    Depress Anxiety; 2022 Jun; 39(6):474-484. PubMed ID: 35312124
    [TBL] [Abstract][Full Text] [Related]  

  • 2. De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism.
    Cappi C; Oliphant ME; Péter Z; Zai G; Conceição do Rosário M; Sullivan CAW; Gupta AR; Hoffman EJ; Virdee M; Olfson E; Abdallah SB; Willsey AJ; Shavitt RG; Miguel EC; Kennedy JL; Richter MA; Fernandez TV
    Biol Psychiatry; 2020 Jun; 87(12):1035-1044. PubMed ID: 31771860
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rare de novo damaging DNA variants are enriched in attention-deficit/hyperactivity disorder and implicate risk genes.
    Olfson E; Farhat LC; Liu W; Vitulano LA; Zai G; Lima MO; Parent J; Polanczyk GV; Cappi C; Kennedy JL; Fernandez TV
    Nat Commun; 2024 Jul; 15(1):5870. PubMed ID: 38997333
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Exome-wide Analysis of De Novo and Rare Genetic Variants in Patients With Brain Arteriovenous Malformation.
    Wang K; Zhao S; Xie Z; Zhang M; Zhao H; Cheng X; Zhang Y; Niu Y; Liu J; Zhang TJ; Zhang Y; Wu Z; Chu J; Yang X; Wu N
    Neurology; 2022 Apr; 98(16):e1670-e1678. PubMed ID: 35228337
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.
    Chen R; Davis LK; Guter S; Wei Q; Jacob S; Potter MH; Cox NJ; Cook EH; Sutcliffe JS; Li B
    Mol Autism; 2017; 8():14. PubMed ID: 28344757
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exome Sequencing of Familial Bipolar Disorder.
    Goes FS; Pirooznia M; Parla JS; Kramer M; Ghiban E; Mavruk S; Chen YC; Monson ET; Willour VL; Karchin R; Flickinger M; Locke AE; Levy SE; Scott LJ; Boehnke M; Stahl E; Moran JL; Hultman CM; Landén M; Purcell SM; Sklar P; Zandi PP; McCombie WR; Potash JB
    JAMA Psychiatry; 2016 Jun; 73(6):590-7. PubMed ID: 27120077
    [TBL] [Abstract][Full Text] [Related]  

  • 7. De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
    Willsey AJ; Fernandez TV; Yu D; King RA; Dietrich A; Xing J; Sanders SJ; Mandell JD; Huang AY; Richer P; Smith L; Dong S; Samocha KE; ; ; Neale BM; Coppola G; Mathews CA; Tischfield JA; Scharf JM; State MW; Heiman GA
    Neuron; 2017 May; 94(3):486-499.e9. PubMed ID: 28472652
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Whole Exome Sequencing Identifies Novel De Novo Variants Interacting with Six Gene Networks in Autism Spectrum Disorder.
    Kim N; Kim KH; Lim WJ; Kim J; Kim SA; Yoo HJ
    Genes (Basel); 2020 Dec; 12(1):. PubMed ID: 33374967
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exome sequencing in obsessive-compulsive disorder reveals a burden of rare damaging coding variants.
    Halvorsen M; Samuels J; Wang Y; Greenberg BD; Fyer AJ; McCracken JT; Geller DA; Knowles JA; Zoghbi AW; Pottinger TD; Grados MA; Riddle MA; Bienvenu OJ; Nestadt PS; Krasnow J; Goes FS; Maher B; Nestadt G; Goldstein DB
    Nat Neurosci; 2021 Aug; 24(8):1071-1076. PubMed ID: 34183866
    [TBL] [Abstract][Full Text] [Related]  

  • 10. De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders.
    Qi H; Yu L; Zhou X; Wynn J; Zhao H; Guo Y; Zhu N; Kitaygorodsky A; Hernan R; Aspelund G; Lim FY; Crombleholme T; Cusick R; Azarow K; Danko ME; Chung D; Warner BW; Mychaliska GB; Potoka D; Wagner AJ; ElFiky M; Wilson JM; Nickerson D; Bamshad M; High FA; Longoni M; Donahoe PK; Chung WK; Shen Y
    PLoS Genet; 2018 Dec; 14(12):e1007822. PubMed ID: 30532227
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DIAPH1 Variants in Non-East Asian Patients With Sporadic Moyamoya Disease.
    Kundishora AJ; Peters ST; Pinard A; Duran D; Panchagnula S; Barak T; Miyagishima DF; Dong W; Smith H; Ocken J; Dunbar A; Nelson-Williams C; Haider S; Walker RL; Li B; Zhao H; Thumkeo D; Marlier A; Duy PQ; Diab NS; Reeves BC; Robert SM; Sujijantarat N; Stratman AN; Chen YH; Zhao S; Roszko I; Lu Q; Zhang B; Mane S; Castaldi C; López-Giráldez F; Knight JR; Bamshad MJ; Nickerson DA; Geschwind DH; Chen SL; Storm PB; Diluna ML; Matouk CC; Orbach DB; Alper SL; Smith ER; Lifton RP; Gunel M; Milewicz DM; Jin SC; Kahle KT
    JAMA Neurol; 2021 Aug; 78(8):993-1003. PubMed ID: 34125151
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Whole-Exome Sequencing Study of Tourette Disorder in a Chinese Population.
    Zhao X; Wang S; Hao J; Zhu P; Zhang X; Wu M
    DNA Cell Biol; 2020 Jan; 39(1):63-68. PubMed ID: 31855460
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH.
    Zhu N; Swietlik EM; Welch CL; Pauciulo MW; Hagen JJ; Zhou X; Guo Y; Karten J; Pandya D; Tilly T; Lutz KA; Martin JM; Treacy CM; Rosenzweig EB; Krishnan U; Coleman AW; Gonzaga-Jauregui C; Lawrie A; Trembath RC; Wilkins MR; ; ; ; ; Morrell NW; Shen Y; Gräf S; Nichols WC; Chung WK
    Genome Med; 2021 May; 13(1):80. PubMed ID: 33971972
    [TBL] [Abstract][Full Text] [Related]  

  • 14. De novo variation in bipolar disorder.
    Goes FS; Pirooznia M; Tehan M; Zandi PP; McGrath J; Wolyniec P; Nestadt G; Pulver AE
    Mol Psychiatry; 2021 Aug; 26(8):4127-4136. PubMed ID: 31776463
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort.
    da Silva Montenegro EM; Costa CS; Campos G; Scliar M; de Almeida TF; Zachi EC; Silva IMW; Chan AJS; Zarrei M; Lourenço NCV; Yamamoto GL; Scherer S; Passos-Bueno MR
    Autism Res; 2020 Feb; 13(2):199-206. PubMed ID: 31696658
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rare variants and de novo variants in mesial temporal lobe epilepsy with hippocampal sclerosis.
    Wong JKL; Gui H; Kwok M; Ng PW; Lui CHT; Baum L; Sham PC; Kwan P; Cherny SS
    Neurol Genet; 2018 Jun; 4(3):e245. PubMed ID: 29904720
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Exome-Based Case-Control Analysis Highlights the Pathogenic Role of Ciliary Genes in Transposition of the Great Arteries.
    Liu X; Chen W; Li W; Priest JR; Fu Y; Pang K; Ma B; Han B; Liu X; Hu S; Zhou Z
    Circ Res; 2020 Mar; 126(7):811-821. PubMed ID: 32078439
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database.
    Li J; Cai T; Jiang Y; Chen H; He X; Chen C; Li X; Shao Q; Ran X; Li Z; Xia K; Liu C; Sun ZS; Wu J
    Mol Psychiatry; 2016 Feb; 21(2):290-7. PubMed ID: 25849321
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease.
    Ognenovski M; Renauer P; Gensterblum E; Kötter I; Xenitidis T; Henes JC; Casali B; Salvarani C; Direskeneli H; Kaufman KM; Sawalha AH
    Arthritis Rheumatol; 2016 May; 68(5):1272-80. PubMed ID: 26662719
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene.
    Qiao L; Xu L; Yu L; Wynn J; Hernan R; Zhou X; Farkouh-Karoleski C; Krishnan US; Khlevner J; De A; Zygmunt A; Crombleholme T; Lim FY; Needelman H; Cusick RA; Mychaliska GB; Warner BW; Wagner AJ; Danko ME; Chung D; Potoka D; Kosiński P; McCulley DJ; Elfiky M; Azarow K; Fialkowski E; Schindel D; Soffer SZ; Lyon JB; Zalieckas JM; Vardarajan BN; Aspelund G; Duron VP; High FA; Sun X; Donahoe PK; Shen Y; Chung WK
    Am J Hum Genet; 2021 Oct; 108(10):1964-1980. PubMed ID: 34547244
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.