BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 35961607)

  • 1. CHDbase: A Comprehensive Knowledgebase for Congenital Heart Disease-related Genes and Clinical Manifestations.
    Zhou WZ; Li W; Shen H; Wang RW; Chen W; Zhang Y; Zeng Q; Wang H; Yuan M; Zeng Z; Cui J; Li CY; Ye FY; Zhou Z
    Genomics Proteomics Bioinformatics; 2023 Feb; 21(1):216-227. PubMed ID: 35961607
    [TBL] [Abstract][Full Text] [Related]  

  • 2. CHDGKB: a knowledgebase for systematic understanding of genetic variations associated with non-syndromic congenital heart disease.
    Yang L; Yang Y; Liu X; Chen Y; Chen Y; Lin Y; Sun Y; Shen B
    Database (Oxford); 2020 Jan; 2020():. PubMed ID: 32608479
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetics and Genomics of Congenital Heart Disease.
    Zaidi S; Brueckner M
    Circ Res; 2017 Mar; 120(6):923-940. PubMed ID: 28302740
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and genetic findings in patients with congenital cataract and heart diseases.
    Li X; Si N; Song Z; Ren Y; Xiao W
    Orphanet J Rare Dis; 2021 May; 16(1):242. PubMed ID: 34059112
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Investigation of Genetic Causes in Patients with Congenital Heart Disease in Qatar: Findings from the Sidra Cardiac Registry.
    Okashah S; Vasudeva D; El Jerbi A; Khodjet-El-Khil H; Al-Shafai M; Syed N; Kambouris M; Udassi S; Saraiva LR; Al-Saloos H; Udassi J; Al-Shafai KN
    Genes (Basel); 2022 Jul; 13(8):. PubMed ID: 36011280
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular insight into heart development and congenital heart disease: An update review from the Arab countries.
    Aburawi EH; Aburawi HE; Bagnall KM; Bhuiyan ZA
    Trends Cardiovasc Med; 2015 May; 25(4):291-301. PubMed ID: 25541328
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CHD@ZJU: a knowledgebase providing network-based research platform on coronary heart disease.
    Wu L; Li X; Yang J; Liu Y; Fan X; Cheng Y
    Database (Oxford); 2013; 2013():bat047. PubMed ID: 23818526
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of dysfunctional modules and disease genes in congenital heart disease by a network-based approach.
    He D; Liu ZP; Chen L
    BMC Genomics; 2011 Dec; 12():592. PubMed ID: 22136190
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Epidemiology, etiology and clinical associations of congenital heart disease identified during congenital rubella syndrome surveillance.
    Priyanka P; Vyas V; Deora S; Nag VL; Singh K
    J Trop Pediatr; 2022 Oct; 68(6):. PubMed ID: 36306124
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.
    LaHaye S; Corsmeier D; Basu M; Bowman JL; Fitzgerald-Butt S; Zender G; Bosse K; McBride KL; White P; Garg V
    Circ Cardiovasc Genet; 2016 Aug; 9(4):320-9. PubMed ID: 27418595
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic considerations for adults with congenital heart disease.
    Ito S; Chapman KA; Kisling M; John AS
    Am J Med Genet C Semin Med Genet; 2020 Mar; 184(1):149-153. PubMed ID: 32052945
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield.
    Geng J; Picker J; Zheng Z; Zhang X; Wang J; Hisama F; Brown DW; Mullen MP; Harris D; Stoler J; Seman A; Miller DT; Fu Q; Roberts AE; Shen Y
    BMC Genomics; 2014 Dec; 15(1):1127. PubMed ID: 25516202
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The Congenital Heart Disease Genetic Network Study: rationale, design, and early results.
    ; Gelb B; Brueckner M; Chung W; Goldmuntz E; Kaltman J; Kaski JP; Kim R; Kline J; Mercer-Rosa L; Porter G; Roberts A; Rosenberg E; Seiden H; Seidman C; Sleeper L; Tennstedt S; Kaltman J; Schramm C; Burns K; Pearson G; Rosenberg E
    Circ Res; 2013 Feb; 112(4):698-706. PubMed ID: 23410879
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Maternal sociodemographic characteristics, early pregnancy behaviours, and livebirth outcomes as congenital heart defects risk factors - Northern Ireland 2010-2014.
    Saad H; Sinclair M; Bunting B
    BMC Pregnancy Childbirth; 2021 Nov; 21(1):759. PubMed ID: 34758755
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic Contribution to Congenital Heart Disease (CHD).
    Shabana NA; Shahid SU; Irfan U
    Pediatr Cardiol; 2020 Jan; 41(1):12-23. PubMed ID: 31872283
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data.
    Szot JO; Cuny H; Blue GM; Humphreys DT; Ip E; Harrison K; Sholler GF; Giannoulatou E; Leo P; Duncan EL; Sparrow DB; Ho JWK; Graham RM; Pachter N; Chapman G; Winlaw DS; Dunwoodie SL
    Circ Genom Precis Med; 2018 Mar; 11(3):e001978. PubMed ID: 29555671
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Reassessment of Copy Number Variations in Congenital Heart Defects: Picturing the Whole Genome.
    Meerschaut I; Vergult S; Dheedene A; Menten B; De Groote K; De Wilde H; Muiño Mosquera L; Panzer J; Vandekerckhove K; Coucke PJ; De Wolf D; Callewaert B
    Genes (Basel); 2021 Jul; 12(7):. PubMed ID: 34356064
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dynamics in prevalence of Down syndrome in children with congenital heart disease.
    Pfitzer C; Helm PC; Rosenthal LM; Berger F; Bauer UMM; Schmitt KR
    Eur J Pediatr; 2018 Jan; 177(1):107-115. PubMed ID: 29127498
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Incidence of congenital heart defects in the Czech Republic--current data].
    Sípek A; Gregor V; Sípek A; Hudáková J; Horácek J; Klaschka J; Skibová J; Langhammer P; Petrzílková L; Klímová B; Perinová B; Wiesnerová J
    Ceska Gynekol; 2010 May; 75(3):221-42. PubMed ID: 20731304
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Consanguinity and Congenital Heart Disease Susceptibility: Insights into Rare Genetic Variations in Saudi Arabia.
    Albesher N; Massadeh S; Hassan SM; Alaamery M
    Genes (Basel); 2022 Feb; 13(2):. PubMed ID: 35205398
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.