Literature DB >> 16707752

Newborn hearing screening--a silent revolution.

Cynthia C Morton1, Walter E Nance.   

Abstract

Mesh：

Year:  2006        PMID： 16707752     DOI： 10.1056/NEJMra050700

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  495 in total

1.  Unilateral hearing loss is associated with worse speech-language scores in children.

Authors:  Judith E C Lieu; Nancy Tye-Murray; Roanne K Karzon; Jay F Piccirillo
Journal:  Pediatrics       Date:  2010-05-10       Impact factor: 7.124

2.  A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss.

Authors:  Asli Sirmaci; Seyra Erbek; Justin Price; Mingqian Huang; Duygu Duman; F Başak Cengiz; Güney Bademci; Suna Tokgöz-Yilmaz; Burcu Hişmi; Hilal Ozdağ; Banu Oztürk; Sevsen Kulaksizoğlu; Erkan Yildirim; Haris Kokotas; Maria Grigoriadou; Michael B Petersen; Hashem Shahin; Moien Kanaan; Mary-Claire King; Zheng-Yi Chen; Susan H Blanton; Xue Z Liu; Stephan Zuchner; Nejat Akar; Mustafa Tekin
Journal:  Am J Hum Genet       Date:  2010-05-06       Impact factor: 11.025

3.  Saliva polymerase-chain-reaction assay for cytomegalovirus screening in newborns.

Authors:  Suresh B Boppana; Shannon A Ross; Masako Shimamura; April L Palmer; Amina Ahmed; Marian G Michaels; Pablo J Sánchez; David I Bernstein; Robert W Tolan; Zdenek Novak; Nazma Chowdhury; William J Britt; Karen B Fowler
Journal:  N Engl J Med       Date:  2011-06-02       Impact factor: 91.245

4.  Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment.

Authors:  Lauren J Francey; Laura K Conlin; Hanna E Kadesch; Dinah Clark; Donna Berrodin; Yi Sun; Joe Glessner; Hakon Hakonarson; Chaim Jalas; Chaim Landau; Nancy B Spinner; Margaret Kenna; Michal Sagi; Heidi L Rehm; Ian D Krantz
Journal:  Am J Med Genet A       Date:  2011-12-06       Impact factor: 2.802

Review 5.  Public health and laboratory considerations regarding newborn screening for congenital cytomegalovirus.

Authors:  Sheila C Dollard; Mark R Schleiss; Scott D Grosse
Journal:  J Inherit Metab Dis       Date:  2010-06-08       Impact factor: 4.982

Review 6.  Genetics of hearing loss: where are we standing now?

Authors:  Hossein Mahboubi; Sami Dwabe; Matthew Fradkin; Virginia Kimonis; Hamid R Djalilian
Journal:  Eur Arch Otorhinolaryngol       Date:  2012-01-05       Impact factor: 2.503

Review 7.  Applications of targeted gene capture and next-generation sequencing technologies in studies of human deafness and other genetic disabilities.

Authors:  Xi Lin; Wenxue Tang; Shoeb Ahmad; Jingqiao Lu; Candice C Colby; Jason Zhu; Qing Yu
Journal:  Hear Res       Date:  2012-01-14       Impact factor: 3.208

8.  A low-cost exon capture method suitable for large-scale screening of genetic deafness by the massively-parallel sequencing approach.

Authors:  Wenxue Tang; Dong Qian; Shoeb Ahmad; Douglas Mattox; N Wendell Todd; Harrison Han; Shouting Huang; Yuhua Li; Yunfeng Wang; Huawei Li; Xi Lin
Journal:  Genet Test Mol Biomarkers       Date:  2012-04-05

9.  Audiologic and temporal bone imaging findings in patients with sensorineural hearing loss and GJB2 mutations.

Authors:  Kenneth H Lee; Daniel A Larson; Gordon Shott; Brian Rasmussen; Aliza P Cohen; Corning Benton; Mark Halsted; Daniel Choo; Jareen Meinzen-Derr; John H Greinwald
Journal:  Laryngoscope       Date:  2009-03       Impact factor: 3.325

10.  Requirements for guinea pig cytomegalovirus tropism and antibody neutralization on placental amniotic sac cells.

Authors:  K Yeon Choi; Nadia S El-Hamdi; Alistair McGregor
Journal:  J Gen Virol       Date:  2020-02-18       Impact factor: 3.891
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