Suffian N. Khan, Ph.D. - Publications

2014 Physics University of Illinois, Urbana-Champaign, Urbana-Champaign, IL 
computational physics

11 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2014 Khan SN, Johnson DD. Lifshitz transition and chemical instabilities in Ba(1-x)K(x)Fe2As2 superconductors. Physical Review Letters. 112: 156401. PMID 24785059 DOI: 10.1103/Physrevlett.112.156401  0.456
2014 Rehman AU, Santos-Cortez RL, Morell RJ, Drummond MC, Ito T, Lee K, Khan AA, Basra MA, Wasif N, Ayub M, Ali RA, Raza SI, Nickerson DA, Shendure J, ... ... Khan SN, et al. Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86. American Journal of Human Genetics. 94: 144-52. PMID 24387994 DOI: 10.1016/J.Ajhg.2013.12.004  0.466
2014 Alam A, Khan SN, Smirnov AV, Nicholson DM, Johnson DD. Green's function multiple-scattering theory with a truncated basis set: An augmented-KKR formalism Physical Review B - Condensed Matter and Materials Physics. 90. DOI: 10.1103/Physrevb.90.205102  0.456
2014 Khan SN, Alam A, Johnson DD. Fermi surfaces and phase stability of Ba(Fe1-xMx)2 As2 (M=Co,Ni,Cu,Zn) Physical Review B - Condensed Matter and Materials Physics. 89. DOI: 10.1103/Physrevb.89.205121  0.446
2013 Khan SN, Alam A, Johnson DD. Low-energy planar magnetic defects in BaFe2As2: Nanotwins, twins, antiphase, and domain boundaries Physical Review B - Condensed Matter and Materials Physics. 88. DOI: 10.1103/Physrevb.88.184515  0.46
2012 Kim MG, Lamsal J, Heitmann TW, Tucker GS, Pratt DK, Khan SN, Lee YB, Alam A, Thaler A, Ni N, Ran S, Bud'Ko SL, Marty KJ, Lumsden MD, Canfield PC, et al. Effects of transition metal substitutions on the incommensurability and spin fluctuations in BaFe 2As 2 by elastic and inelastic neutron scattering Physical Review Letters. 109. DOI: 10.1103/PhysRevLett.109.167003  0.447
2011 Riazuddin S, Ahmed ZM, Hegde RS, Khan SN, Nasir I, Shaukat U, Riazuddin S, Butman JA, Griffith AJ, Friedman TB, Choi BY. Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome. Bmc Medical Genetics. 12: 21. PMID 21306635 DOI: 10.1186/1471-2350-12-21  0.424
2007 Ain Q, Nazli S, Riazuddin S, Jaleel AU, Riazuddin SA, Zafar AU, Khan SN, Husnain T, Griffith AJ, Ahmed ZM, Friedman TB, Riazuddin S. The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3. Human Genetics. 122: 445-50. PMID 17690910 DOI: 10.1007/s00439-007-0418-z  0.451
2003 Ahmed ZM, Morell RJ, Riazuddin S, Gropman A, Shaukat S, Ahmad MM, Mohiddin SA, Fananapazir L, Caruso RC, Husnain T, Khan SN, Riazuddin S, Griffith AJ, Friedman TB, Wilcox ER. Mutations of MYO6 are associated with recessive deafness, DFNB37. American Journal of Human Genetics. 72: 1315-22. PMID 12687499 DOI: 10.1086/375122  0.46
2002 Bork JM, Morell RJ, Khan S, Riazuddin S, Wilcox ER, Friedman TB, Griffith AJ. Clinical presentation of DFNB12 and Usher syndrome type 1D. Advances in Oto-Rhino-Laryngology. 61: 145-52. PMID 12408077 DOI: 10.1159/000066829  0.419
2002 Kurima K, Peters LM, Yang Y, Riazuddin S, Ahmed ZM, Naz S, Arnaud D, Drury S, Mo J, Makishima T, Ghosh M, Menon PS, Deshmukh D, Oddoux C, Ostrer H, ... Khan S, et al. Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function. Nature Genetics. 30: 277-84. PMID 11850618 DOI: 10.1038/Ng842  0.763
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