Concepedia

Author

Shangzhen Zhou

Children's Hospital of Philadelphia

Also Known As

Merricks, Elizabeth, S Zhou, Shang-Zhen Zhou, Shangzhen Zhou, Zhou, Shangzhen

86

Publications

6.8K

Citations

42

H-Index

72

Concepts

All Affiliations

Children's Hospital of PhiladelphiaUniversity of PennsylvaniaHoward Hughes Medical InstituteUniversity of North Carolina at Chapel HillIndiana University School of Medicine
SZ

About

Shangzhen Zhou is an author at Children's Hospital of Philadelphia specializing in medicine, immunology, and virology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

14

14

2K

2

Health Sciences

2

2

132

3

Allergy

2

2

110

4

Engineering

1

1

540

5

Social Sciences

1

1

27

Shangzhen Zhou

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57

Publications

6.7K

Citations

42

H-Index

YearCitations

In vivo genome editing restores haemostasis in a mouse model of haemophilia

Hojun Li, Virginia Haurigot, Yannick Doyon,

Nature

2011

540

Human fibroblast growth factor receptor 1 is a co-receptor for infection by adeno-associated virus 2

Keyun Qing, Cathryn Mah, Jonathan J. Hansen,

Nature Medicine

1999

431

Effects of transient immunosuppression on adenoassociated, virus-mediated, liver-directed gene transfer in rhesus macaques and implications for human gene therapy

Haiyan Jiang, Linda B. Couto, Susannah Patarroyo‐White,

Blood

2006

316

In vivo genome editing of the albumin locus as a platform for protein replacement therapy

Rajiv P. Sharma, Xavier M. Anguela, Yannick Doyon,

Blood

2015

295

Therapeutic levels of FVIII following a single peripheral vein administration of rAAV vector encoding a novel human factor VIII variant

Jenny McIntosh, Peter J. Lenting, Cecilia Rosales,

Blood

2013

269

Human immunoglobulin inhibits liver transduction by AAV vectors at low AAV2 neutralizing titers in SCID mice

Ciaran D. Scallan, Haiyan Jiang, Tongyao Liu,

Blood

2005

260

Reversal of Blindness in Animal Models of Leber Congenital Amaurosis Using Optimized AAV2-mediated Gene Transfer

Jeannette Bennicelli, J. Fraser Wright, András M. Komáromy,

Molecular Therapy

2008

260

Modulation of tolerance to the transgene product in a nonhuman primate model of AAV-mediated gene transfer to liver

Federico Mingozzi, Nicole C. Hasbrouck, Etiena Basner‐Tschakarjan,

Blood

2007

245

Preclinical in vivo evaluation of pseudotyped adeno-associated virus vectors for liver gene therapy

Dirk Grimm, Shangzhen Zhou, Hiroyuki Nakai,

Blood

2003

204

Multiyear therapeutic benefit of AAV serotypes 2, 6, and 8 delivering factor VIII to hemophilia A mice and dogs

Haiyan Jiang, David Lillicrap, Susannah Patarroyo‐White,

Blood

2006

197

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