Author details

Full Name

Amin R Mazloom

Affiliation

ORCID

Career Start Year

2010

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
35344790	Analytical validation of a novel panel of biomarkers for a test for preeclampsia.	Journal of Pharmaceutical and Biomedical Analysis	2022
35652095	Esrrb Regulates Specific Feed-Forward Loops to Transit From Pluripotency Into Early Stages of Differentiation.	Frontiers in Cell and Developmental Biology	2022
35545947	Performance of a Multianalyte 'Rule-Out' Assay in Pregnant Individuals With Suspected Preeclampsia.	Hypertension	2022
34465593	Genome-wide Sequencing of Cell-free DNA Enables Detection of Copy-number Alterations in Patients with Cancer Where Tissue Biopsy is Not Feasible.	Mol Cancer Ther	2021
34285421	Publisher Correction: A systems approach identifies HIPK2 as a key regulator of kidney fibrosis.	Nat Med	2021
33816475	An Esrrb and Nanog Cell Fate Regulatory Module Controlled by Feed Forward Loop Interactions.	Front Cell Dev Biol	2021
30523049	Genome-Wide Sequencing of Cell-Free DNA Identifies Copy-Number Alterations That Can Be Used for Monitoring Response to Immunotherapy in Cancer Patients.	Mol Cancer Ther	2019
28617416	Genome-wide cfDNA screening: clinical laboratory experience with the first 10,000 cases.	Genetics in Medicine	2017
27694391	Using Targeted Sequencing of Paralogous Sequences for Noninvasive Detection of Selected Fetal Aneuploidies.	Clin Chem	2016
26899906	Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants.	American Journal of Obstetrics and Gynecology	2016
26505614	Application of risk score analysis to low-coverage whole genome sequencing data for the noninvasive detection of trisomy 21, trisomy 18, and trisomy 13.	Prenat Diagn	2016
25967380	Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts.	Prenat Diagn	2015
25289665	Non-invasive prenatal chromosomal aneuploidy testing--clinical experience: 100,000 clinical samples.	PLoS ONE	2014
23702428	ELK1 transcription factor linked to dysregulated striatal mu opioid receptor signaling network and OPRM1 polymorphism in human heroin abusers.	Biol Psychiatry	2013
23483908	High-throughput massively parallel sequencing for fetal aneuploidy detection from maternal plasma.	PLoS ONE	2013
23592550	Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell-free DNA from maternal plasma.	Prenatal Diagnosis	2013
23023392	Gene-expression profiles and transcriptional regulatory pathways that underlie the identity and diversity of mouse tissue macrophages.	Nat Immunol	2012
22869928	Activation of alternate prosurvival pathways accounts for acquired sunitinib resistance in U87MG glioma xenografts.	J Pharmacol Exp Ther	2012
22406746	A systems approach identifies HIPK2 as a key regulator of kidney fibrosis.	Nat Med	2012
23153495	Sox2 in the dermal papilla niche controls hair growth by fine-tuning BMP signaling in differentiating hair shaft progenitors.	Dev Cell	2012
22219718	Recovering protein-protein and domain-domain interactions from aggregation of IP-MS proteomics of coregulator complexes.	PLoS Comput Biol	2011
19945504	Chromatin remodeling in silico: a stochastic model for SWI/SNF.	BioSystems	2010
20709693	ChEA: transcription factor regulation inferred from integrating genome-wide ChIP-X experiments.	Bioinformatics	2010
20703299	Mesenchymal and haematopoietic stem cells form a unique bone marrow niche.	Nature	2010