User profiles for "author:Lisa Allen"

Lisa Zeigler Allen

J. Craig Venter Institute, Scripps Institution of Oceanography
Verified email at jcvi.org
Cited by 3566

[HTML][HTML] Minimum information about an uncultivated virus genome (MIUViG)

S Roux, EM Adriaenssens, BE Dutilh, EV Koonin… - Nature …, 2019 - nature.com
We present an extension of the Minimum Information about any (x) Sequence (MIxS)
standard for reporting sequences of uncultivated virus genomes. Minimum Information about …

Müllerian duct anomalies and mimics in children and adolescents: correlative intraoperative assessment with clinical imaging

BLP Junqueira, LM Allen, RF Spitzer, KL Lucco… - Radiographics, 2009 - pubs.rsna.org
Müllerian duct anomalies (MDAs) are congenital entities that result from nondevelopment,
defective vertical or lateral fusion, or resorption failure of the müllerian (paramesonephric) …

No. 383-screening, diagnosis, and management of placenta accreta spectrum disorders

SR Hobson, JC Kingdom, A Murji, RC Windrim… - Journal of Obstetrics and …, 2019 - Elsevier
Background Placenta accreta spectrum (PAS) disorders are a potentially life-threatening
complication of pregnancy that demand coordinated interdisciplinary care to achieve safer …

Endometriosis: diagnosis and management

N Leyland, R Casper, P Laberge… - Journal of …, 2010 - journals.sagepub.com
Objective To improve the understanding of endometriosis and to provide evidence-based
guidelines for the diagnosis and management of endometriosis. Outcomes Outcomes …

[PDF][PDF] Expansion of the global RNA virome reveals diverse clades of bacteriophages

U Neri, YI Wolf, S Roux, AP Camargo, B Lee… - Cell, 2022 - cell.com
High-throughput RNA sequencing offers broad opportunities to explore the Earth RNA
virome. Mining 5,150 diverse metatranscriptomes uncovered> 2.5 million RNA virus contigs …

[PDF][PDF] Mutations in the hepatocyte nuclear factor-1β gene are associated with familial hypoplastic glomerulocystic kidney disease

C Bingham, MP Bulman, S Ellard, LIS Allen… - The American Journal of …, 2001 - cell.com
Familial glomerulocystic kidney disease (GCKD) is a dominantly inherited condition
characterized by glomerular cysts and variable renal size and function; the molecular …

[HTML][HTML] Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes

WM Macfarlane, TM Frayling, S Ellard… - The Journal of …, 1999 - Am Soc Clin Investig
The transcription factor insulin promoter factor-1 (IPF-1) plays a central role in both the
development of the pancreas and the regulation of insulin gene expression in the mature …

beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors.

TM Frayling, JC Evans, MP Bulman, E Pearson… - Diabetes, 2001 - Am Diabetes Assoc
beta-Cell transcription factor genes are important in the pathophysiology of the beta-cell,
with mutations in hepatocyte nuclear factor (HNF)-1alpha, HNF-4alpha, insulin promoter …

Association of psychiatric manifestations with antibodies to ribosomal P proteins in systemic lupus erythematosus

AB Schneebaum, JD Singleton, SG West… - The American journal of …, 1991 - Elsevier
Abstract purpose: The goal of this study was to determine whether elevated serum levels of
antibodies to ribosomal P proteins (anti-P antibodies) are associated with neuropsychiatric …

[PDF][PDF] FIGO consensus guidelines on placenta accreta spectrum disorders: nonconservative surgical management

L Allen, E Jauniaux, S Hobson… - … of Gynecology & …, 2018 - discovery.ucl.ac.uk
For more than half a century after the first case series of placenta accreta was reported in
1937 [1], the main and often only approach to management was the cesarean hysterectomy …