458 related articles for article (PubMed ID: 29654098)
1. Functional Assays to Screen and Dissect Genomic Hits: Doubling Down on the National Investment in Genomic Research.
Musunuru K; Bernstein D; Cole FS; Khokha MK; Lee FS; Lin S; McDonald TV; Moskowitz IP; Quertermous T; Sankaran VG; Schwartz DA; Silverman EK; Zhou X; Hasan AAK; Luo XJ
Circ Genom Precis Med; 2018 Apr; 11(4):e002178. PubMed ID: 29654098
[TBL] [Abstract][Full Text] [Related]
2. Genome analysis and knowledge-driven variant interpretation with TGex.
Dahary D; Golan Y; Mazor Y; Zelig O; Barshir R; Twik M; Iny Stein T; Rosner G; Kariv R; Chen F; Zhang Q; Shen Y; Safran M; Lancet D; Fishilevich S
BMC Med Genomics; 2019 Dec; 12(1):200. PubMed ID: 31888639
[TBL] [Abstract][Full Text] [Related]
3. Rare-variant genome-wide association studies: a new frontier in genetic analysis of complex traits.
Wagner MJ
Pharmacogenomics; 2013 Mar; 14(4):413-24. PubMed ID: 23438888
[TBL] [Abstract][Full Text] [Related]
4. Genomic Analysis in the Age of Human Genome Sequencing.
Lappalainen T; Scott AJ; Brandt M; Hall IM
Cell; 2019 Mar; 177(1):70-84. PubMed ID: 30901550
[TBL] [Abstract][Full Text] [Related]
5. Cardiovascular genomics, personalized medicine, and the National Heart, Lung, and Blood Institute: part I: the beginning of an era.
O'Donnell CJ; Nabel EG
Circ Cardiovasc Genet; 2008 Oct; 1(1):51-7. PubMed ID: 20031542
[TBL] [Abstract][Full Text] [Related]
6. Rationale and study design of the CardioGene Study: genomics of in-stent restenosis.
Ganesh SK; Skelding KA; Mehta L; O'Neill K; Joo J; Zheng G; Goldstein J; Simari R; Billings E; Geller NL; Holmes D; O'Neill WW; Nabel EG
Pharmacogenomics; 2004 Oct; 5(7):952-1004. PubMed ID: 15469413
[TBL] [Abstract][Full Text] [Related]
7. Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients.
Lim EC; Brett M; Lai AH; Lee SP; Tan ES; Jamuar SS; Ng IS; Tan EC
Hum Genomics; 2015 Dec; 9():33. PubMed ID: 26666243
[TBL] [Abstract][Full Text] [Related]
8. Identification of clinically actionable variants from genome sequencing of families with congenital heart disease.
Alankarage D; Ip E; Szot JO; Munro J; Blue GM; Harrison K; Cuny H; Enriquez A; Troup M; Humphreys DT; Wilson M; Harvey RP; Sholler GF; Graham RM; Ho JWK; Kirk EP; Pachter N; Chapman G; Winlaw DS; Giannoulatou E; Dunwoodie SL
Genet Med; 2019 May; 21(5):1111-1120. PubMed ID: 30293987
[TBL] [Abstract][Full Text] [Related]
9. When "
Cassa CA; Akle S; Jordan DM; Rosenfeld JA
Cold Spring Harb Mol Case Stud; 2017 May; 3(3):a001099. PubMed ID: 28487880
[TBL] [Abstract][Full Text] [Related]
10. Overview of high throughput sequencing technologies to elucidate molecular pathways in cardiovascular diseases.
Churko JM; Mantalas GL; Snyder MP; Wu JC
Circ Res; 2013 Jun; 112(12):1613-23. PubMed ID: 23743227
[TBL] [Abstract][Full Text] [Related]
11. Gene and Variant Annotation for Mendelian Disorders in the Era of Advanced Sequencing Technologies.
Chakravorty S; Hegde M
Annu Rev Genomics Hum Genet; 2017 Aug; 18():229-256. PubMed ID: 28415856
[TBL] [Abstract][Full Text] [Related]
12. Insights into genetics, human biology and disease gleaned from family based genomic studies.
Posey JE; O'Donnell-Luria AH; Chong JX; Harel T; Jhangiani SN; Coban Akdemir ZH; Buyske S; Pehlivan D; Carvalho CMB; Baxter S; Sobreira N; Liu P; Wu N; Rosenfeld JA; Kumar S; Avramopoulos D; White JJ; Doheny KF; Witmer PD; Boehm C; Sutton VR; Muzny DM; Boerwinkle E; Günel M; Nickerson DA; Mane S; MacArthur DG; Gibbs RA; Hamosh A; Lifton RP; Matise TC; Rehm HL; Gerstein M; Bamshad MJ; Valle D; Lupski JR;
Genet Med; 2019 Apr; 21(4):798-812. PubMed ID: 30655598
[TBL] [Abstract][Full Text] [Related]
13. Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Green RC; Goddard KAB; Jarvik GP; Amendola LM; Appelbaum PS; Berg JS; Bernhardt BA; Biesecker LG; Biswas S; Blout CL; Bowling KM; Brothers KB; Burke W; Caga-Anan CF; Chinnaiyan AM; Chung WK; Clayton EW; Cooper GM; East K; Evans JP; Fullerton SM; Garraway LA; Garrett JR; Gray SW; Henderson GE; Hindorff LA; Holm IA; Lewis MH; Hutter CM; Janne PA; Joffe S; Kaufman D; Knoppers BM; Koenig BA; Krantz ID; Manolio TA; McCullough L; McEwen J; McGuire A; Muzny D; Myers RM; Nickerson DA; Ou J; Parsons DW; Petersen GM; Plon SE; Rehm HL; Roberts JS; Robinson D; Salama JS; Scollon S; Sharp RR; Shirts B; Spinner NB; Tabor HK; Tarczy-Hornoch P; Veenstra DL; Wagle N; Weck K; Wilfond BS; Wilhelmsen K; Wolf SM; Wynn J; Yu JH;
Am J Hum Genet; 2016 Jun; 98(6):1051-1066. PubMed ID: 27181682
[TBL] [Abstract][Full Text] [Related]
14. Functional Studies of Genetic Variants Associated with Human Diseases in Notch Signaling-Related Genes Using Drosophila.
Yang SA; Salazar JL; Li-Kroeger D; Yamamoto S
Methods Mol Biol; 2022; 2472():235-276. PubMed ID: 35674905
[TBL] [Abstract][Full Text] [Related]
15. Rare variant association test with multiple phenotypes.
Lee S; Won S; Kim YJ; Kim Y; ; Kim BJ; Park T
Genet Epidemiol; 2017 Apr; 41(3):198-209. PubMed ID: 28039885
[TBL] [Abstract][Full Text] [Related]
16. Genome sequencing in the clinic: the past, present, and future of genomic medicine.
Prokop JW; May T; Strong K; Bilinovich SM; Bupp C; Rajasekaran S; Worthey EA; Lazar J
Physiol Genomics; 2018 Aug; 50(8):563-579. PubMed ID: 29727589
[TBL] [Abstract][Full Text] [Related]
17. Genomic prediction using preselected DNA variants from a GWAS with whole-genome sequence data in Holstein-Friesian cattle.
Veerkamp RF; Bouwman AC; Schrooten C; Calus MP
Genet Sel Evol; 2016 Dec; 48(1):95. PubMed ID: 27905878
[TBL] [Abstract][Full Text] [Related]
18. Sequencing-based diagnostics for pediatric genetic diseases: progress and potential.
Abou Tayoun AN; Krock B; Spinner NB
Expert Rev Mol Diagn; 2016 Sep; 16(9):987-99. PubMed ID: 27388938
[TBL] [Abstract][Full Text] [Related]
19. A practical guide to filtering and prioritizing genetic variants.
Jalali Sefid Dashti M; Gamieldien J
Biotechniques; 2017 Jan; 62(1):18-30. PubMed ID: 28118812
[TBL] [Abstract][Full Text] [Related]
20. Genomics of Alzheimer's disease: Value of high-throughput genomic technologies to dissect its etiology.
Tosto G; Reitz C
Mol Cell Probes; 2016 Dec; 30(6):397-403. PubMed ID: 27618776
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]