Rochelle Hirschhorn - Publications, H-index & Citations

Rochelle Hirschhorn

New York University

54H指数

196论文数

9.4K被引数

收录论文 11

发表时间

A Conversation with Kurt and Rochelle Hirschhorn

ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS

IF0

2017-08-31

OAAI

Hirschhorn, Kurt; Hirschhorn, Rochelle; Hirschhorn, Joel N.

De Minimis Risk: A Proposal for a New Category of Research Risk 最小风险: 一种新的研究风险类别的建议

AMERICAN JOURNAL OF BIOETHICS

IF20.8

2011-11-01

PREAI

Rhodes, Rosamond; Azzouni, Jody; Baumrin, Stefan Bernard; Benkov, Keith; Blaser, Martin J.; Brenner, Barbara; Dauben, Joseph W.; Earle, William J.; Frank, Lily; Gligorov, Nada; Goldfarb, Joseph; Hirschhorn, Kurt; Hirschhorn, Rochelle; Holzman, Ian; Indyk, Debbie; Jabs, Ethylin Wang; Lackey, Douglas P.; Moros, Daniel A.; Philpott, Sean; Rhodes, Matthew E.; Richardson, Lynne D.; Sacks, Henry S.; Schwab, Abraham; Sperling, Rhoda; Trusko, Brett; Zweig, Arnulf

Homozygosity for multiple contiguous single-nucleotide polymorphisms as an indicator of large heterozygous deletions: Identification of a novel heterozygous 8-kb intragenic deletion (IVS7-19 to IVS15-17) in a patient with glycogen storage disease type II

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2002-04-01

OAAI

Huie, ML; Anyane-Yeboa, K; Guzman, E; Hirschhorn, R

SCID in Jack Russell terriers: A new animal model of DNA-PKcs deficiency

JOURNAL OF IMMUNOLOGY

IF3.4

2001-08-15

PREAI

Meek, K; Kienker, L; Dallas, C; Wang, W; Dark, MJ; Venta, PJ; Huie, ML; Hirschhorn, R; Bell, T

Reverse mutations - spontaneous amelioration or cure of inherited disorders?

EUROPEAN JOURNAL OF PEDIATRICS

IF2.6

1998-07-27

PREAI

Wahn, V; Stephan, V; Hirschhorn, R

The African origin of the common mutation in African American patients with glycogen-storage disease type II

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

1998-04-01

OAAI

Becker, JA; Vlach, J; Raben, N; Nagaraju, K; Adams, EM; Hermans, MM; Reuser, AJJ; Brooks, SS; Tifft, CJ; Hirschhorn, R; Huie, ML; Nicolino, M; Plotz, PH

Wound healing is accelerated by agonists of adenosine A(2) (G(alpha s)-linked) receptors

JOURNAL OF EXPERIMENTAL MEDICINE

IF10.6

1997-11-03

188

OAAI

Montesinos, MC; Gadangi, P; Longaker, M; Sung, J; Levine, J; Nilsen, D; Reibman, J; Li, M; Jiang, CK; Hirschhorn, R; Recht, PA; Ostad, E; Levin, RI; Cronstein, BN

Two newly identified mutations (Thr233Ile and Leu152Met) in partially adenosine deaminase-deficient (ADA(-)) individuals that result in differing biochemical and metabolic phenotypes

HUMAN GENETICS

IF3.6

1997-06-19

PREAI

Hirschhorn, R; Borkowsky, W; Jiang, CK; Yang, DR; Jenkins, T

Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency

NATURE GENETICS

IF31.8

1996-07-01

199

PREAI