Author details

Full Name

Elise A Feingold

Affiliation

ORCID

Career Start Year

1983

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
33116284	Strategic vision for improving human health at The Forefront of Genomics.	Nature	2020
25164755	Comparative analysis of the transcriptome across distant species.	Nature	2014
25409824	A comparative encyclopedia of DNA elements in the mouse genome.	Nature	2014
25275169	Reply to Brunet and Doolittle: Both selected effect and causal role elements can influence human biology and disease.	Proc Natl Acad Sci U S A	2014
24753594	Defining functional DNA elements in the human genome.	Proc Natl Acad Sci U S A	2014
25164756	Comparative analysis of metazoan chromatin organization.	Nature	2014
25164757	Comparative analysis of regulatory information and circuits across distant species.	Nature	2014
22889292	An encyclopedia of mouse DNA elements (Mouse ENCODE).	Genome Biol	2012
21177974	Identification of functional elements and regulatory circuits by Drosophila modENCODE.	Science	2010
21177976	Integrative analysis of the Caenorhabditis elegans genome by the modENCODE project.	Science	2010
19767417	The completion of the Mammalian Gene Collection (MGC).	Genome Res	2009
17571346	Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.	Nature	2007
12477932	Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.	Proc Natl Acad Sci U S A	2002
10521335	The mammalian gene collection.	Science	1999
10512676	An olfactory receptor gene is located in the extended human beta-globin gene cluster and is expressed in erythroid cells.	Genomics	1999
10116049	The homeless elderly.		1991
2478223	The breakpoint of a large deletion causing hereditary persistence of fetal hemoglobin occurs within an erythroid DNA domain remote from the beta-globin gene cluster.	Blood	1989
2409868	Molecular analysis of deletion and nondeletion hereditary persistence of fetal hemoglobin and identification of a new mutation causing beta-thalassemia.	Ann N Y Acad Sci	1985
2413468	Analysis of mutations associated with deletion and nondeletion hereditary persistence of fetal hemoglobin.	Prog Clin Biol Res	1985
6196781	Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man.	Proceedings of the National Academy of Sciences of the United States of America	1983
6198666	Molecular studies of mutations that increase Hb F production in man.	Progress in Clinical and Biological Research	1983