310 related articles for article (PubMed ID: 27855690)
1. The continuum of causality in human genetic disorders.
Katsanis N
Genome Biol; 2016 Nov; 17(1):233. PubMed ID: 27855690
[TBL] [Abstract][Full Text] [Related]
2. Magnitude of Mendelian versus complex inheritance of rare disorders.
Chakravarti A
Am J Med Genet A; 2021 Nov; 185(11):3287-3293. PubMed ID: 34418293
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Beyond Mendel: an evolving view of human genetic disease transmission.
Badano JL; Katsanis N
Nat Rev Genet; 2002 Oct; 3(10):779-89. PubMed ID: 12360236
[TBL] [Abstract][Full Text] [Related]
5. The role of genes in disease: beware of simplistic interpretations!
Prescrire Int; 2009 Dec; 18(104):279-82. PubMed ID: 20027720
[TBL] [Abstract][Full Text] [Related]
6. Genomics shifts focus to rare diseases.
Check Hayden E
Nature; 2009 Sep; 461(7263):458. PubMed ID: 19779424
[No Abstract] [Full Text] [Related]
7. Exome sequencing as a tool for Mendelian disease gene discovery.
Bamshad MJ; Ng SB; Bigham AW; Tabor HK; Emond MJ; Nickerson DA; Shendure J
Nat Rev Genet; 2011 Sep; 12(11):745-55. PubMed ID: 21946919
[TBL] [Abstract][Full Text] [Related]
8. Searching for genetic determinants in the new millennium.
Risch NJ
Nature; 2000 Jun; 405(6788):847-56. PubMed ID: 10866211
[TBL] [Abstract][Full Text] [Related]
9. Genome-wide strategies for detecting multiple loci that influence complex diseases.
Marchini J; Donnelly P; Cardon LR
Nat Genet; 2005 Apr; 37(4):413-7. PubMed ID: 15793588
[TBL] [Abstract][Full Text] [Related]
10. Genetic Modifiers and Rare Mendelian Disease.
Rahit KMTH; Tarailo-Graovac M
Genes (Basel); 2020 Feb; 11(3):. PubMed ID: 32106447
[TBL] [Abstract][Full Text] [Related]
11. Finding the missing heritability of complex diseases.
Manolio TA; Collins FS; Cox NJ; Goldstein DB; Hindorff LA; Hunter DJ; McCarthy MI; Ramos EM; Cardon LR; Chakravarti A; Cho JH; Guttmacher AE; Kong A; Kruglyak L; Mardis E; Rotimi CN; Slatkin M; Valle D; Whittemore AS; Boehnke M; Clark AG; Eichler EE; Gibson G; Haines JL; Mackay TF; McCarroll SA; Visscher PM
Nature; 2009 Oct; 461(7265):747-53. PubMed ID: 19812666
[TBL] [Abstract][Full Text] [Related]
12. Complex genetic diseases: controversy over the Croesus code.
Wright AF; Hastie ND
Genome Biol; 2001; 2(8):COMMENT2007. PubMed ID: 11532206
[TBL] [Abstract][Full Text] [Related]
13. Using gene genealogies to detect rare variants associated with complex traits.
Burkett KM; McNeney B; Graham J; Greenwood CM
Hum Hered; 2014; 78(3-4):117-30. PubMed ID: 25138120
[TBL] [Abstract][Full Text] [Related]
14. Human genetics: conceptual and practical advances in the post-genome era.
Davies K; Wynshaw-Boris A
Curr Opin Genet Dev; 2009 Jun; 19(3):193-5. PubMed ID: 19481439
[No Abstract] [Full Text] [Related]
15. The great beyond.
Nature; 2012 Feb; 483(7387):5-6. PubMed ID: 22382938
[No Abstract] [Full Text] [Related]
16. [Prospects of medicinal use of achievements in genomics: the beginning of era of complete genome medical genetics].
Sverdlov ED
Patol Fiziol Eksp Ter; 2001; (1):3-22. PubMed ID: 11247299
[No Abstract] [Full Text] [Related]
17. Integration of genetics into medical practice.
Korf BR
Growth Horm IGF Res; 2004 Jun; 14 Suppl A():S146-9. PubMed ID: 15135799
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. On not reinventing the wheel.
Nat Genet; 2012 Feb; 44(3):233. PubMed ID: 22366856
[TBL] [Abstract][Full Text] [Related]
20. Approaches to identify genes for complex human diseases: lessons from Mendelian disorders.
Dean M
Hum Mutat; 2003 Oct; 22(4):261-74. PubMed ID: 12955713
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
