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au.\*:("MUZNY, Donna M")

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High incidence of IDH mutations in acute myeloid leukaemia with cuplike nucleiRAKHEJA, Dinesh; KONOPLEV, Sergej; CHEN, Weina et al.British journal of haematology. 2011, Vol 155, Num 1, pp 125-128, issn 0007-1048, 4 p.Article

The finished DNA sequence of human chromosome 12SCHERER, Steven E; MUZNY, Donna M; HAWES, Alicia C et al.Nature (London). 2006, Vol 440, Num 7082, pp 346-351, issn 0028-0836, 6 p.Article

Strict evolutionary conservation followed rapid gene loss on human and rhesus Y chromosomesHUGHES, Jennifer F; SKALETSKY, Helen; QIAOYAN WANG et al.Nature (London). 2012, Vol 483, Num 7387, pp 82-86, issn 0028-0836, 5 p.Article

The complete genome of an individual by massively parallel DNA sequencingWHEELER, David A; SRINIVASAN, Maithreyan; GOMES, Xavier et al.Nature (London). 2008, Vol 452, Num 7189, pp 872-876, issn 0028-0836, 5 p.Article

The genome sequence of Mannheimia haemolytica A1 : Insights into virulence, natural competence, and Pasteurellaceae phylogenyGIOIA, Jason; XIANG QIN; HEMPHILL, Lisa et al.Journal of bacteriology. 2006, Vol 188, Num 20, pp 7257-7266, issn 0021-9193, 10 p.Article

Whole-Exome Sequencing Identifies Compound Heterozygous Mutations in WDR62 in Siblings With Recurrent PolymicrogyriaMURDOCK, David R; CLARK, Gary D; BAINBRIDGE, Matthew N et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 9, pp 2071-2077, issn 1552-4825, 7 p.Article

Whole-Genome Sequencing in a Patient with Charcot―Marie―Tooth NeuropathyLUPSKI, James R; REID, Jefrey G; MCGUIRE, Amy L et al.The New England journal of medicine. 2010, Vol 362, Num 13, pp 1181-1191, issn 0028-4793, 11 p.Article

A Collagen-Binding Adhesin, Acb, and Ten Other Putative MSCRAMM and Pilus Family Proteins of Streptococcus gallolyticus subsp. gallolyticus (Streptococcus bovis Group, Biotype I)SILLANPÄÄ, Jouko; NALLAPAREDDY, Sreedhar R; WEINSTOCK, George M et al.Journal of bacteriology. 2009, Vol 191, Num 21, pp 6643-6653, issn 0021-9193, 11 p.Article

TTC21B contributes both causal and modifying alleles across the ciliopathy spectrumDAVIS, Erica E; QI ZHANG; MUZNY, Donna M et al.Nature genetics. 2011, Vol 43, Num 3, pp 189-196, issn 1061-4036, 8 p.Article

Exome Sequencing of Head and Neck Squamous Cell Carcinoma Reveals Inactivating Mutations in NOTCH1AGRAWAL, Nishant; FREDERICK, Mitchell J; NIANXIANG ZHANG et al.Science (Washington, D.C.). 2011, Vol 333, Num 6046, pp 1154-1157, issn 0036-8075, 4 p.Article

Mutations in Smooth Muscle Alpha-Actin (ACTA2) Cause Coronary Artery Disease, Stroke, and Moyamoya Disease, Along with Thoracic Aortic DiseaseGUO, Dong-Chuan; PAPKE, Christina L; PYERITZ, Reed E et al.American journal of human genetics. 2009, Vol 84, Num 5, pp 617-627, issn 0002-9297, 11 p.Article

The DNA sequence, annotation and analysis of human chromosome 3MUZNY, Donna M; SCHERER, Steven E; DUGAN-ROCHA, Shannon et al.Nature (London). 2006, Vol 440, Num 7088, pp 1194-1198, issn 0028-0836, 5 p.Article

Molecular Findings Among Patients Referred for Clinical Whole-Exome SequencingYAPING YANG; MUZNY, Donna M; VEERARAGHAVAN, Narayanan et al.JAMA, the journal of the American Medical Association. 2014, Vol 312, Num 18, pp 1870-1879, issn 0098-7484, 10 p.Article

Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian DisordersYAPING YANG; MUZNY, Donna M; HARDISON, Matthew et al.The New England journal of medicine. 2013, Vol 369, Num 16, pp 1502-1511, issn 0028-4793, 10 p.Article

Complete Khoisan and Bantu genomes from southern AfricaSCHUSTER, Stephan C; MILLER, Webb; ALKAN, Can et al.Nature (London). 2010, Vol 463, Num 7283, pp 943-947, issn 0028-0836, 5 p.Article

Somatic mutations affect key pathways in lung adenocarcinomaLI DING; GETZ, Gad; FULTON, Lucinda et al.Nature (London). 2008, Vol 455, Num 7216, pp 1069-1075, issn 0028-0836, 7 p.Article

Comparative and demographic analysis of orang-utan genomesLOCKE, Devin P; HILLIER, Ladeana W; MITREVA, Makedonka et al.Nature (London). 2011, Vol 469, Num 7331, pp 529-533, issn 0028-0836, 5 p.Article

A high-resolution map of human evolutionary constraint using 29 mammalsKERSTIN, Lindblad- Toh; GARBER, Manuel; WARD, Lucas D et al.Nature (London). 2011, Vol 478, Num 7370, pp 476-482, issn 0028-0836, 7 p.Article

A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathiesKHANNA, Hemant; DAVIS, Erica E; MAUBARET, Cecilia et al.Nature genetics. 2009, Vol 41, Num 6, pp 739-745, issn 1061-4036, 7 p.Article

Common and Rare Variants of DAOA in Bipolar DisorderMAHESHWARI, Manjula; JIAJUN SHI; POTASH, James B et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2009, Vol 150, Num 7, pp 960-966, issn 1552-4841, 7 p.Article

The Complete Genome Sequence of Escherichia coli DH10B : Insights into the Biology of a Laboratory WorkhorseDURFEE, Tim; NELSON, Richard; GIBBS, Richard A et al.Journal of bacteriology. 2008, Vol 190, Num 7, pp 2597-2606, issn 0021-9193, 10 p.Article

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