logo
科言猫学术研究的AI总结
language
手机端手机端
  • Phone Feature微信小程序
简体中文简体中文
notice消息通知
博客博客
delete
arrow
返回
M

Matthew J. McGinniss

university of south florida

25H指数
93论文数
2.6K被引数
收录论文 18
发表时间
logo
Co-existence of SRSF2 and EZH2 gene mutations in myeloid malignancies
errCANCER RESEARCH
IF16.6
err2017-07-01
err0
PREAI
errCherukuri, Durga P.; Kwok, Brian; Lekostaj, Jacqueline; Petersen, Paris; Bui, Peter; Nooraie, Farzad; Cheng, Li; Fike, Francesca; Taylor, David A.; Dabbas, Bashar; Mcginniss, Matthew J.
err分享
err收藏
Impact of TP53 mutation variant allele frequency on phenotype and outcomes in myelodysplastic syndromes
errLEUKEMIA
IF13.4
err2015-10-30
err182
errOAAI
errSallman, D. A.; Komrokji, R.; Vaupel, C.; Cluzeau, T.; Geyer, S. M.; McGraw, K. L.; Al Ali, N. H.; Lancet, J.; McGinniss, M. J.; Nahas, S.; Smith, A. E.; Kulasekararaj, A.; Mufti, G.; List, A.; Hall, J.; Padron, E.
err分享
err收藏
Identification of critical steps involved in optimization of next generation sequencing (NGS) using a retrospective meta-analysis of a large clinical testing cohort
errCANCER RESEARCH
IF16.6
err2014-10-01
err0
PREAI
errMurphy, Danielle A.; Scott, Christopher; Fitzgerald, Kerry; Panjikaran, Maya; Xia, Yu; Graber, Armin; Kines, Julie; Baer, Adam; McGinniss, Matthew; Christiansen, Jason
err分享
err收藏
Identification of HRAS mutations and absence of GNAQ or GNA11 mutations in deep penetrating nevi
errMODERN PATHOLOGY
IF5.5
err2013-10-01
err31
errOAAI
errBender, Ryan P.; McGinniss, Matthew J.; Esmay, Paula; Velazquez, Elsa F.; Reimann, Julie D. R.
err分享
err收藏
Implementing an automated clinical next generation sequencing analysis pipeline - assuring accurate and robust results.
errCANCER RESEARCH
IF16.6
err2013-04-01
err0
PREAI
errBaer, Adam; Xia, Yu; Holscher, Todd; Loper, Robyn; McGinniss, Matthew J.; Tseng, Richard; Kines, Julie; Diver, Jonathan; Christiansen, Jason
err分享
err收藏
KRAS and BRAF mutation spectrum in 1,035 FFPE tumor samples submitted for clinical testing
errCANCER RESEARCH
IF16.6
err2010-04-01
err0
PREAI
errBender, Ryan P.; McGinniss, Matthew J.; Dejesa-Jamanila, Liza; Kuslich, Christine
err分享
err收藏
Characterization of a recurrent novel large duplication in the cystic fibrosis transmembrane conductance regulator gene
errJOURNAL OF MOLECULAR DIAGNOSTICS
IF3.4
err2007-09-01
err18
errOAAI
errHantash, Feras M.; Redman, Joy B.; Goos, Dana; Kammesheidt, Anja; McGinniss, Matthew J.; Sun, Weimin; Strom, Charles M.
err分享
err收藏
Development of a web-based query tool for quality assurance of clinical molecular genetic test results
errJOURNAL OF MOLECULAR DIAGNOSTICS
IF3.4
err2007-02-01
err2
errOAAI
errMcGinniss, Matthew J.; Chen, Rebecca; Pratt, Victoria M.; Buller, Arlene; Quan, Franklin; Strom, Charles M.; Sun, Weimin; Crossley, Beryl
err分享
err收藏
Technical validation of a Tm biosciences luminex-based multiplex assay for detecting the American College of Medical Genetics Recommended Cystic Fibrosis Mutation Panel
errJOURNAL OF MOLECULAR DIAGNOSTICS
IF3.4
err2006-07-01
err19
errOAAI
errStrom, Charles M.; Janeszco, Richard; Quan, Franklin; Wang, Sheng-biao; Buller, Arlene; McGinniss, Matthew; Sun, Weimin
err分享
err收藏
CFTR 5T variant has a low penetrance in females that is partially attributable to its haplotypeCFTR 5t变体在女性中的外显率较低，部分归因于其单倍型
errGENETICS IN MEDICINE
IF6.2
err2006-06-01
err22
errOAAI
errSun, Weimin; Anderson, Ben; Redman, Joy; Milunsky, Aubrey; Buller, Arlene; McGinniss, Matthew J.; Quan, Franklin; Anguiano, Arturo; Huang, Stephen; Hantash, Feras; Strom, Charles
err分享
err收藏
Novel and recurrent rearrangements in the CFTR gene:: clinical and laboratory implications for cystic fibrosis screening (vol 95, pg 361, 2000)
errHUMAN GENETICS
IF3.6
err2006-02-11
err1
errOAAI
errHantash, FM; Redman, JB; Starn, K; Anderson, B; Buller, A; McGinniss, MJ; Quan, F; Peng, M; Sun, WM; Strom, CM
err分享
err收藏
Novel and recurrent rearrangements in the CFTR gene:: clinical and laboratory implications for cystic fibrosis screening
errHUMAN GENETICS
IF3.6
err2005-12-17
err37
PREAI
errHantash, FM; Redman, JB; Starn, K; Anderson, B; Buller, A; McGinniss, MJ; Quan, F; Peng, M; Sun, WM; Strom, CM
err分享
err收藏
Technical validation of a multiplex platform to detect thirty mutations in eight genetic diseases prevalent in individuals of Ashkenazi Jewish descent
errGENETICS IN MEDICINE
IF6.2
err2005-11-01
err12
errOAAI
errStrom, CM; Janeczko, RA; Anderson, B; Redman, J; Quan, F; Buller, A; McGinniss, MJ; Sun, WM
err分享
err收藏
Extensive Sequencing of the CFTR gene: lessons learned from the first 157 patient samples
errHUMAN GENETICS
IF3.6
err2005-09-28
err34
PREAI
errMcGinniss, MJ; Chen, C; Redman, JB; Buller, A; Quan, F; Peng, M; Giusti, R; Hantash, FM; Huang, DH; Sun, WM; Strom, CM
err分享
err收藏
Detection of 677CT/1298AC double variant chromosomes:: Implications for interpretation of MTHFR genotyping results
errGENETICS IN MEDICINE
IF6.2
err2005-04-01
err21
errOAAI
errBrown, NM; Pratt, VM; Buller, A; Pike-Buchanan, L; Redman, JB; Sun, WM; Chen, R; Crossley, B; McGinniss, MJ; Quan, F; Strom, CM
err分享
err收藏
Molecular screening for diseases frequent in Ashkenazi Jews: Lessons learned from more than 100,000 tests performed in a commercial laboratory
errGENETICS IN MEDICINE
IF6.2
err2004-05-01
err24
errOAAI
errStrom, CM; Crossley, B; Redman, JB; Quan, F; Buller, A; McGinniss, MJ; Sun, WM
err分享
err收藏
Technology challenges in screening single gene disorders
errEUROPEAN JOURNAL OF PEDIATRICS
IF2.6
err2003-12-01
err12
PREAI
errBraun, A; Richard, R; McGinniss, MJ
err分享
err收藏
Eight novel mutations in the HEXA gene
errGENETICS IN MEDICINE
IF6.2
err2002-05-01
err7
errOAAI
errMcGinniss, MJ; Brown, DH; Fulwiler, A; Marten, M; Lim-Steele, JST; Kaback, MM
err分享
err收藏

研究方向

暂时未获取到该数据
合作学者
合作期刊
A
Alan F. List
H 指数: 89 · 论文数: 1.0K
C
Christopher G. Scott
H 指数: 78 · 论文数: 772
R
Rami S. Komrokji
H 指数: 68 · 论文数: 1.5K
J
Jeffrey E. Lancet
H 指数: 62 · 论文数: 881
A
Austin Kulasekararaj
H 指数: 55 · 论文数: 461
查看更多