491 related articles for article (PubMed ID: 28332277)
1. Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder.
Kim DS; Burt AA; Ranchalis JE; Wilmot B; Smith JD; Patterson KE; Coe BP; Li YK; Bamshad MJ; Nikolas M; Eichler EE; Swanson JM; Nigg JT; Nickerson DA; Jarvik GP;
Am J Med Genet B Neuropsychiatr Genet; 2017 Jun; 174(4):381-389. PubMed ID: 28332277
[TBL] [Abstract][Full Text] [Related]
2. Pathogenic variants in
Granadillo JL; P A Stegmann A; Guo H; Xia K; Angle B; Bontempo K; Ranells JD; Newkirk P; Costin C; Viront J; Stumpel CT; Sinnema M; Panis B; Pfundt R; Krapels IPC; Klaassens M; Nicolai J; Li J; Jiang Y; Marco E; Canton A; Latronico AC; Montenegro L; Leheup B; Bonnet C; M Amudhavalli S; Lawson CE; McWalter K; Telegrafi A; Pearson R; Kvarnung M; Wang X; Bi W; Rosenfeld JA; Shinawi M
J Med Genet; 2020 Oct; 57(10):717-724. PubMed ID: 32152250
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder.
Mirzaa GM; Chong JX; Piton A; Popp B; Foss K; Guo H; Harripaul R; Xia K; Scheck J; Aldinger KA; Sajan SA; Tang S; Bonneau D; Beck A; White J; Mahida S; Harris J; Smith-Hicks C; Hoyer J; Zweier C; Reis A; Thiel CT; Jamra RA; Zeid N; Yang A; Farach LS; Walsh L; Payne K; Rohena L; Velinov M; Ziegler A; Schaefer E; Gatinois V; Geneviève D; Simon MEH; Kohler J; Rotenberg J; Wheeler P; Larson A; Ernst ME; Akman CI; Westman R; Blanchet P; Schillaci LA; Vincent-Delorme C; Gripp KW; Mattioli F; Guyader GL; Gerard B; Mathieu-Dramard M; Morin G; Sasanfar R; Ayub M; Vasli N; Yang S; Person R; Monaghan KG; Nickerson DA; van Binsbergen E; Enns GM; Dries AM; Rowe LJ; Tsai ACH; Svihovec S; Friedman J; Agha Z; Qamar R; Rodan LH; Martinez-Agosto J; Ockeloen CW; Vincent M; Sunderland WJ; Bernstein JA; ; Eichler EE; Vincent JB; ; Bamshad MJ
Genet Med; 2020 Mar; 22(3):538-546. PubMed ID: 31723249
[TBL] [Abstract][Full Text] [Related]
5. Inattention and hyperactivity/impulsivity among children with attention-deficit/hyperactivity-disorder, autism spectrum disorder, and intellectual disability.
McClain MB; Hasty Mills AM; Murphy LE
Res Dev Disabil; 2017 Nov; 70():175-184. PubMed ID: 28957735
[TBL] [Abstract][Full Text] [Related]
6. A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder.
Martin J; Hosking G; Wadon M; Agha SS; Langley K; Rees E; Owen MJ; O'Donovan M; Kirov G; Thapar A
Transl Psychiatry; 2020 May; 10(1):135. PubMed ID: 32398668
[TBL] [Abstract][Full Text] [Related]
7. Language deficits in specific language impairment, attention deficit/hyperactivity disorder, and autism spectrum disorder: An analysis of polygenic risk.
Nudel R; Christiani CAJ; Ohland J; Uddin MJ; Hemager N; Ellersgaard DV; Spang KS; Burton BK; Greve AN; Gantriis DL; Bybjerg-Grauholm J; Jepsen JRM; Thorup AAE; Mors O; Nordentoft M; Werge T
Autism Res; 2020 Mar; 13(3):369-381. PubMed ID: 31577390
[TBL] [Abstract][Full Text] [Related]
8. Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants.
Satterstrom FK; Walters RK; Singh T; Wigdor EM; Lescai F; Demontis D; Kosmicki JA; Grove J; Stevens C; Bybjerg-Grauholm J; Bækvad-Hansen M; Palmer DS; Maller JB; ; Nordentoft M; Mors O; Robinson EB; Hougaard DM; Werge TM; Bo Mortensen P; Neale BM; Børglum AD; Daly MJ
Nat Neurosci; 2019 Dec; 22(12):1961-1965. PubMed ID: 31768057
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior.
Harris HK; Nakayama T; Lai J; Zhao B; Argyrou N; Gubbels CS; Soucy A; Genetti CA; Suslovitch V; Rodan LH; Tiller GE; Lesca G; Gripp KW; Asadollahi R; Hamosh A; Applegate CD; Turnpenny PD; Simon MEH; Volker-Touw CML; Gassen KLIV; Binsbergen EV; Pfundt R; Gardeitchik T; Vries BBA; Immken LL; Buchanan C; Willing M; Toler TL; Fassi E; Baker L; Vansenne F; Wang X; Ambrus JL; Fannemel M; Posey JE; Agolini E; Novelli A; Rauch A; Boonsawat P; Fagerberg CR; Larsen MJ; Kibaek M; Labalme A; Poisson A; Payne KK; Walsh LE; Aldinger KA; Balciuniene J; Skraban C; Gray C; Murrell J; Bupp CP; Pascolini G; Grammatico P; Broly M; Küry S; Nizon M; Rasool IG; Zahoor MY; Kraus C; Reis A; Iqbal M; Uguen K; Audebert-Bellanger S; Ferec C; Redon S; Baker J; Wu Y; Zampino G; Syrbe S; Brosse I; Jamra RA; Dobyns WB; Cohen LL; Blomhoff A; Mignot C; Keren B; Courtin T; Agrawal PB; Beggs AH; Yu TW
Genet Med; 2021 Jun; 23(6):1028-1040. PubMed ID: 33658631
[TBL] [Abstract][Full Text] [Related]
12. Genetic Relationships between Attention-Deficit/Hyperactivity Disorder, Autism Spectrum Disorder, and Intelligence.
Rao S; Baranova A; Yao Y; Wang J; Zhang F
Neuropsychobiology; 2022; 81(6):484-496. PubMed ID: 35764056
[TBL] [Abstract][Full Text] [Related]
13. PLXNA2 and LRRC40 as candidate genes in autism spectrum disorder.
Pijuan J; Ortigoza-Escobar JD; Ortiz J; Alcalá A; Calvo MJ; Cubells M; Hernando-Davalillo C; Palau F; Hoenicka J
Autism Res; 2021 Jun; 14(6):1088-1100. PubMed ID: 33749153
[TBL] [Abstract][Full Text] [Related]
14. Increased risk of ADHD in families with ASD.
Septier M; Peyre H; Amsellem F; Beggiato A; Maruani A; Poumeyreau M; Amestoy A; Scheid I; Gaman A; Bolognani F; Honey G; Bouquet C; Ly-Le Moal M; Bouvard M; Leboyer M; Bourgeron T; Delorme R
Eur Child Adolesc Psychiatry; 2019 Feb; 28(2):281-288. PubMed ID: 30267210
[TBL] [Abstract][Full Text] [Related]
15. Exome Sequencing of Two Siblings with Sporadic Autism Spectrum Disorder and Severe Speech Sound Disorder Suggests Pleiotropic and Complex Effects.
Peter B; Dinu V; Liu L; Huentelman M; Naymik M; Lancaster H; Vose C; Schrauwen I
Behav Genet; 2019 Jul; 49(4):399-414. PubMed ID: 30949922
[TBL] [Abstract][Full Text] [Related]
16. Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation.
Farzin F; Perry H; Hessl D; Loesch D; Cohen J; Bacalman S; Gane L; Tassone F; Hagerman P; Hagerman R
J Dev Behav Pediatr; 2006 Apr; 27(2 Suppl):S137-44. PubMed ID: 16685180
[TBL] [Abstract][Full Text] [Related]
17. Genetic Evidence for Elevated Pathogenicity of Mitochondrial DNA Heteroplasmy in Autism Spectrum Disorder.
Wang Y; Picard M; Gu Z
PLoS Genet; 2016 Oct; 12(10):e1006391. PubMed ID: 27792786
[TBL] [Abstract][Full Text] [Related]
18. Combining multivariate genomic approaches to elucidate the comorbidity between autism spectrum disorder and attention deficit hyperactivity disorder.
Peyre H; Schoeler T; Liu C; Williams CM; Hoertel N; Havdahl A; Pingault JB
J Child Psychol Psychiatry; 2021 Nov; 62(11):1285-1296. PubMed ID: 34235737
[TBL] [Abstract][Full Text] [Related]
19. Psychiatric Polygenic Risk Scores as Predictor for Attention Deficit/Hyperactivity Disorder and Autism Spectrum Disorder in a Clinical Child and Adolescent Sample.
Jansen AG; Dieleman GC; Jansen PR; Verhulst FC; Posthuma D; Polderman TJC
Behav Genet; 2020 Jul; 50(4):203-212. PubMed ID: 31346826
[TBL] [Abstract][Full Text] [Related]
20. Characterization of intellectual disability and autism comorbidity through gene panel sequencing.
Aspromonte MC; Bellini M; Gasparini A; Carraro M; Bettella E; Polli R; Cesca F; Bigoni S; Boni S; Carlet O; Negrin S; Mammi I; Milani D; Peron A; Sartori S; Toldo I; Soli F; Turolla L; Stanzial F; Benedicenti F; Marino-Buslje C; Tosatto SCE; Murgia A; Leonardi E
Hum Mutat; 2019 Sep; 40(9):1346-1363. PubMed ID: 31209962
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
