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 *

294 related articles for article (PubMed ID: 17668371)

  • 61. Use of medical exome sequencing for identification of underlying genetic defects in NICU: Experience in a cohort of 2303 neonates in China.
    Yang L; Wei Z; Chen X; Hu L; Peng X; Wang J; Lu C; Kong Y; Dong X; Ni Q; Lu Y; Wu B; Wang H; Meirelles K; Tian X; Zhang J; Chang F; Liu L; Li C; You W; Cheng G; Wang L; Cao Y; Chen C; Fang P; Tang S; Zhou W
    Clin Genet; 2022 Jan; 101(1):101-109. PubMed ID: 34671977
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Issues in association analysis: error control in case-control association studies for disease gene discovery.
    Ott J
    Hum Hered; 2004; 58(3-4):171-4. PubMed ID: 15812174
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Making headway with genetic diagnostics of intellectual disabilities.
    Willemsen MH; Kleefstra T
    Clin Genet; 2014 Feb; 85(2):101-10. PubMed ID: 23895455
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing.
    Redin C; Gérard B; Lauer J; Herenger Y; Muller J; Quartier A; Masurel-Paulet A; Willems M; Lesca G; El-Chehadeh S; Le Gras S; Vicaire S; Philipps M; Dumas M; Geoffroy V; Feger C; Haumesser N; Alembik Y; Barth M; Bonneau D; Colin E; Dollfus H; Doray B; Delrue MA; Drouin-Garraud V; Flori E; Fradin M; Francannet C; Goldenberg A; Lumbroso S; Mathieu-Dramard M; Martin-Coignard D; Lacombe D; Morin G; Polge A; Sukno S; Thauvin-Robinet C; Thevenon J; Doco-Fenzy M; Genevieve D; Sarda P; Edery P; Isidor B; Jost B; Olivier-Faivre L; Mandel JL; Piton A
    J Med Genet; 2014 Nov; 51(11):724-36. PubMed ID: 25167861
    [TBL] [Abstract][Full Text] [Related]  

  • 65. The common variants/multiple disease hypothesis of common complex genetic disorders.
    Becker KG
    Med Hypotheses; 2004; 62(2):309-17. PubMed ID: 14962646
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Approximation algorithms for a genetic diagnostics problem.
    Kosaraju SR; Schäffer AA; Biesecker LG
    J Comput Biol; 1998; 5(1):9-26. PubMed ID: 9541868
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Revisiting Mendelian disorders through exome sequencing.
    Ku CS; Naidoo N; Pawitan Y
    Hum Genet; 2011 Apr; 129(4):351-70. PubMed ID: 21331778
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders.
    Brown R; Lee H; Eskin A; Kichaev G; Lohmueller KE; Reversade B; Nelson SF; Pasaniuc B
    Eur J Hum Genet; 2016 Jan; 24(1):113-9. PubMed ID: 25898925
    [TBL] [Abstract][Full Text] [Related]  

  • 69. A family-based association study of PRSS12 and mental retardation in the Qinba mountain region of China.
    Xing L; Zhang K; Dai L; Li F; Guo Y; Huang S; Zheng Z; Zhang F; Gao X
    Psychiatr Genet; 2013 Jun; 23(3):137. PubMed ID: 23344636
    [No Abstract]   [Full Text] [Related]  

  • 70. Exome and whole-genome sequencing for gene discovery: the future is now!
    Majewski J; Rosenblatt DS
    Hum Mutat; 2012 Apr; 33(4):591-2. PubMed ID: 22411407
    [No Abstract]   [Full Text] [Related]  

  • 71. Factors influencing success of clinical genome sequencing across a broad spectrum of disorders.
    Taylor JC; Martin HC; Lise S; Broxholme J; Cazier JB; Rimmer A; Kanapin A; Lunter G; Fiddy S; Allan C; Aricescu AR; Attar M; Babbs C; Becq J; Beeson D; Bento C; Bignell P; Blair E; Buckle VJ; Bull K; Cais O; Cario H; Chapel H; Copley RR; Cornall R; Craft J; Dahan K; Davenport EE; Dendrou C; Devuyst O; Fenwick AL; Flint J; Fugger L; Gilbert RD; Goriely A; Green A; Greger IH; Grocock R; Gruszczyk AV; Hastings R; Hatton E; Higgs D; Hill A; Holmes C; Howard M; Hughes L; Humburg P; Johnson D; Karpe F; Kingsbury Z; Kini U; Knight JC; Krohn J; Lamble S; Langman C; Lonie L; Luck J; McCarthy D; McGowan SJ; McMullin MF; Miller KA; Murray L; Németh AH; Nesbit MA; Nutt D; Ormondroyd E; Oturai AB; Pagnamenta A; Patel SY; Percy M; Petousi N; Piazza P; Piret SE; Polanco-Echeverry G; Popitsch N; Powrie F; Pugh C; Quek L; Robbins PA; Robson K; Russo A; Sahgal N; van Schouwenburg PA; Schuh A; Silverman E; Simmons A; Sørensen PS; Sweeney E; Taylor J; Thakker RV; Tomlinson I; Trebes A; Twigg SR; Uhlig HH; Vyas P; Vyse T; Wall SA; Watkins H; Whyte MP; Witty L; Wright B; Yau C; Buck D; Humphray S; Ratcliffe PJ; Bell JI; Wilkie AO; Bentley D; Donnelly P; McVean G
    Nat Genet; 2015 Jul; 47(7):717-726. PubMed ID: 25985138
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analyses.
    Yan L; Huang L; Xu L; Huang J; Ma F; Zhu X; Tang Y; Liu M; Lian Y; Liu P; Li R; Lu S; Tang F; Qiao J; Xie XS
    Proc Natl Acad Sci U S A; 2015 Dec; 112(52):15964-9. PubMed ID: 26712022
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Clinical utility of a targeted next generation sequencing panel in severe and pediatric onset Mendelian diseases.
    Isik E; Onay H; Atik T; Canda E; Cogulu O; Coker M; Ozkinay F
    Eur J Med Genet; 2019 Oct; 62(10):103725. PubMed ID: 31319225
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardation.
    Wagenstaller J; Spranger S; Lorenz-Depiereux B; Kazmierczak B; Nathrath M; Wahl D; Heye B; Glaser D; Liebscher V; Meitinger T; Strom TM
    Am J Hum Genet; 2007 Oct; 81(4):768-79. PubMed ID: 17847001
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Microsatellites versus Single-Nucleotide Polymorphisms in confidence interval estimation of disease loci.
    Papachristou C; Lin S
    Genet Epidemiol; 2006 Jan; 30(1):3-17. PubMed ID: 16355404
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Genomic disorders 20 years on-mechanisms for clinical manifestations.
    Harel T; Lupski JR
    Clin Genet; 2018 Mar; 93(3):439-449. PubMed ID: 28950406
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Genetics of intellectual disability.
    Ropers HH
    Curr Opin Genet Dev; 2008 Jun; 18(3):241-50. PubMed ID: 18694825
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Novel PGD strategy based on single sperm linkage analysis for carriers of single gene pathogenic variant and chromosome reciprocal translocation.
    Wang Y; Zhu X; Yan Z; Zhi X; Guan S; Kuo Y; Nie Y; Lian Y; Huang J; Wei Y; Liu P; Li R; Qiao J; Yan L
    J Assist Reprod Genet; 2020 May; 37(5):1239-1250. PubMed ID: 32350783
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Population choice in mapping genes for complex diseases.
    Wright AF; Carothers AD; Pirastu M
    Nat Genet; 1999 Dec; 23(4):397-404. PubMed ID: 10581024
    [TBL] [Abstract][Full Text] [Related]  

  • 80. A de novo paradigm for mental retardation.
    Vissers LE; de Ligt J; Gilissen C; Janssen I; Steehouwer M; de Vries P; van Lier B; Arts P; Wieskamp N; del Rosario M; van Bon BW; Hoischen A; de Vries BB; Brunner HG; Veltman JA
    Nat Genet; 2010 Dec; 42(12):1109-12. PubMed ID: 21076407
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.