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 *

108 related articles for article (PubMed ID: 31132892)

  • 21. Localisation of a gene implicated in a severe speech and language disorder.
    Fisher SE; Vargha-Khadem F; Watkins KE; Monaco AP; Pembrey ME
    Nat Genet; 1998 Feb; 18(2):168-70. PubMed ID: 9462748
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Whole genome sequencing and rare variant analysis in essential tremor families.
    Odgerel Z; Sonti S; Hernandez N; Park J; Ottman R; Louis ED; Clark LN
    PLoS One; 2019; 14(8):e0220512. PubMed ID: 31404076
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Whole exome sequencing combined with integrated variant annotation prediction identifies asymptomatic Tangier disease with compound heterozygous mutations in ABCA1 gene.
    Tada H; Kawashiri MA; Nohara A; Saito R; Tanaka Y; Nomura A; Konno T; Sakata K; Fujino N; Takamura T; Inazu A; Mabuchi H; Yamagishi M; Hayashi K
    Atherosclerosis; 2015 Jun; 240(2):324-9. PubMed ID: 25875382
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Exome Sequence Analysis of 14 Families With High Myopia.
    Kloss BA; Tompson SW; Whisenhunt KN; Quow KL; Huang SJ; Pavelec DM; Rosenberg T; Young TL
    Invest Ophthalmol Vis Sci; 2017 Apr; 58(4):1982-1990. PubMed ID: 28384719
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic variation (AFLPs and nuclear microsatellites) in two anagenetically derived endemic species of Myrceugenia (Myrtaceae) on the Juan Fernández Islands, Chile.
    López-Sepúlveda P; Takayama K; Greimler J; Peñailillo P; Crawford DJ; Baeza M; Ruiz E; Kohl G; Tremetsberger K; Gatica A; Letelier L; Novoa P; Novak J; Stuessy TF
    Am J Bot; 2013 Apr; 100(4):722-34. PubMed ID: 23510759
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A likely HOXC4 predisposition variant for Chiari malformations.
    Brockmeyer DL; Cheshier SH; Stevens J; Facelli JC; Rowe K; Heiss JD; Musolf A; Viskochil DH; Allen-Brady KL; Cannon-Albright LA
    J Neurosurg; 2023 Jul; 139(1):266-274. PubMed ID: 36433874
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Strong indication of an extinction-based saturation of the flora on the Pacific Robinson Crusoe Islands.
    Greimler J; Schulze CH; López Sepúlveda P; Novoa P; Gatica A; Reiter K; Wessely J; Baeza C; Peñailillo P; Ruiz E; Stuessy T
    Ecol Evol; 2018 Mar; 8(5):2527-2533. PubMed ID: 29531673
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.
    Lowe JK; Maller JB; Pe'er I; Neale BM; Salit J; Kenny EE; Shea JL; Burkhardt R; Smith JG; Ji W; Noel M; Foo JN; Blundell ML; Skilling V; Garcia L; Sullivan ML; Lee HE; Labek A; Ferdowsian H; Auerbach SB; Lifton RP; Newton-Cheh C; Breslow JL; Stoffel M; Daly MJ; Altshuler DM; Friedman JM
    PLoS Genet; 2009 Feb; 5(2):e1000365. PubMed ID: 19197348
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Decoding the genetics of speech and language.
    Graham SA; Fisher SE
    Curr Opin Neurobiol; 2013 Feb; 23(1):43-51. PubMed ID: 23228431
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Genetic factors in the development of language].
    Sanjuán J; Tolosa A; Colomer-Revuelta J; Ivorra-Martínez J; Llacer B; Jover M
    Rev Neurol; 2010 Mar; 50 Suppl 3():S101-6. PubMed ID: 20200835
    [TBL] [Abstract][Full Text] [Related]  

  • 31. FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum.
    Reuter MS; Riess A; Moog U; Briggs TA; Chandler KE; Rauch A; Stampfer M; Steindl K; Gläser D; Joset P; ; Krumbiegel M; Rabe H; Schulte-Mattler U; Bauer P; Beck-Wödl S; Kohlhase J; Reis A; Zweier C
    J Med Genet; 2017 Jan; 54(1):64-72. PubMed ID: 27572252
    [TBL] [Abstract][Full Text] [Related]  

  • 32. X-Linked Glomerulopathy Due to COL4A5 Founder Variant.
    Barua M; John R; Stella L; Li W; Roslin NM; Sharif B; Hack S; Lajoie-Starkell G; Schwaderer AL; Becknell B; Wuttke M; Köttgen A; Cattran D; Paterson AD; Pei Y
    Am J Kidney Dis; 2018 Mar; 71(3):441-445. PubMed ID: 29198386
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Genetics of specific language impairments].
    Bonneau D; Verny C; Uzé J
    Arch Pediatr; 2004 Oct; 11(10):1213-6. PubMed ID: 15475279
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Finding genes influencing susceptibility to complex diseases in the post-genome era.
    Rannala B
    Am J Pharmacogenomics; 2001; 1(3):203-21. PubMed ID: 12083968
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.
    Callaghan DB; Rogic S; Tan PPC; Calli K; Qiao Y; Baldwin R; Jacobson M; Belmadani M; Holmes N; Yu C; Li Y; Li Y; Kurtzke FE; Kuzeljevic B; Yu AY; Hudson M; Mcaughton AJM; Xu Y; Dionne-Laporte A; Girard S; Liang P; Separovic ER; Liu X; Rouleau G; Pavlidis P; Lewis MES
    Clin Genet; 2019 Sep; 96(3):199-206. PubMed ID: 31038196
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification of Rare Variants Predisposing to Thyroid Cancer.
    Wang Y; Liyanarachchi S; Miller KE; Nieminen TT; Comiskey DF; Li W; Brock P; Symer DE; Akagi K; DeLap KE; He H; Koboldt DC; de la Chapelle A
    Thyroid; 2019 Jul; 29(7):946-955. PubMed ID: 30957677
    [No Abstract]   [Full Text] [Related]  

  • 37. Novel combined variants of LDLR and LDLRAP1 genes causing severe familial hypercholesterolemia.
    Alnouri F; Athar M; Al-Allaf FA; Abduljaleel Z; Taher MM; Bouazzaoui A; Al Ammari D; Karrar H; Albabtain M
    Atherosclerosis; 2018 Oct; 277():425-433. PubMed ID: 30270081
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction.
    Marco EJ; Aitken AB; Nair VP; da Gente G; Gerdes MR; Bologlu L; Thomas S; Sherr EH
    BMC Med Genomics; 2018 May; 11(1):50. PubMed ID: 29801487
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Whole exome sequencing combined with integrated variant annotation prediction identifies a causative myosin essential light chain variant in hypertrophic cardiomyopathy.
    Nomura A; Tada H; Teramoto R; Konno T; Hodatsu A; Won HH; Kathiresan S; Ino H; Fujino N; Yamagishi M; Hayashi K
    J Cardiol; 2016 Feb; 67(2):133-9. PubMed ID: 26443374
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Detecting Familial Aggregation.
    Naj AC; Beaty TH
    Methods Mol Biol; 2017; 1666():133-169. PubMed ID: 28980245
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.