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Journal of Medical Genetics|July 9, 2009
Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairmentS C Sreenath Nagamani, F Zhang, O A Shchelochkov, et al.
JCI Insight|March 15, 2017
Type I interferons regulate susceptibility to inflammation-induced preterm birthMonica Cappelletti, Pietro Presicce, Matthew J Lawson, et al.
NPJ Digital Medicine|March 21, 2020
Continuous, noninvasive wireless monitoring of flow of cerebrospinal fluid through shunts in patients with hydrocephalusSiddharth R Krishnan, Hany M Arafa, Kyeongha Kwon, et al.
JAMA Network Open|February 14, 2022
Comparison of Racial, Ethnic, and Geographic Location Diversity of Participants Enrolled in Clinic-Based vs 2 Remote COVID-19 Clinical TrialsJenell Stewart, Meighan L Krows, Torin T Schaafsma, et al.
Journal of Virology|September 12, 2024
SARS-CoV-2 infection perturbs the gastrointestinal tract and induces modest microbial translocation across the intestinal barrierKelsie Brooks, Christine E Nelson, Cynthia Aguilar, et al.
The Journal of Infectious Diseases|February 12, 2022
Detection and Kinetics of Subgenomic Severe Acute Respiratory Syndrome Coronavirus 2 RNA Viral Load in Longitudinal Diagnostic RNA-Positive SamplesMeagan E Deming, Tracy Q Dong, Vaidehi Agrawal, et al.
Otolaryngologia Polska = the Polish Otolaryngology|August 15, 2012
[Epidemiological and demographic analysis of indications for Baha® surgery in Poland--multicenter study]Witold Szyfter, Lukasz Borucki, Paweł Dobosz, et al.
Human Molecular Genetics|March 1, 2011
Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplicationsPengfei Liu, Ayelet Erez, Sandesh C Sreenath Nagamani, et al.
Journal of Medical Genetics|March 18, 2009
Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disordersS Ben-Shachar, B Lanpher, J R German, et al.
American Journal of Human Genetics|July 29, 2014
The Alu-rich genomic architecture of SPAST predisposes to diverse and functionally distinct disease-associated CNV allelesPhilip M Boone, Bo Yuan, Ian M Campbell, et al.
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