Concepedia

Author

Beverly S. Emanuel

Children's Hospital of PhiladelphiaORCID

Also Known As

B Emanuel, B S EMANUEL, B S Emanuel, B s. Emanuel, B. Emanuel, B. S. Emanuel, B. S.Emanuel, B.S. Emanuel, BEVERLY S. EMANUEL, Bernice Morrow

419

Publications

24.3K

Citations

82

H-Index

232

Concepts

All Affiliations

Children's Hospital of PhiladelphiaUniversity of PennsylvaniaAlbert Einstein College of MedicineHospital of the University of PennsylvaniaThe Wistar Institute
BS

About

Beverly S. Emanuel is an author at Children's Hospital of Philadelphia specializing in medicine, genetics, and molecular genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Health Sciences

11

11

1.8K

2

Arts

3

3

292

3

Education

1

1

215

4

Engineering

1

1

125

5

Language Studies

1

1

110

Beverly S. Emanuel

×

238

Publications

19.9K

Citations

77

H-Index

YearCitations

The DNA sequence of human chromosome 22

Ian Dunham, Adrienne Hunt, John Collins,

Nature

1999

1.2K

Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma

Naomi Galili, Richard J. Davis, William J. Fredericks,

Nature Genetics

1993

899

Frequency of 22q11 deletions in patients with conotruncal defects

Elizabeth Goldmuntz, Bernard J. Clark, Laura E. Mitchell,

Journal of the American College of Cardiology

1998

587

Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma

Frederic G. Barr, Naomi Galili, John Holick,

Nature Genetics

1993

556

Localization of gene for human p53 tumour antigen to band 17p13

Masaharu Isobe, Beverly S. Emanuel, David Givol,

Nature

1986

491

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.

Deborah A. Driscoll, J Salvin, Beatrice Sellinger,

Journal of Medical Genetics

1993

488

Deletions and microdeletions of 22q11.2 in velo‐cardio‐facial syndrome

Deborah A. Driscoll, Nancy B. Spinner, Marcia L. Budarf,

American Journal of Medical Genetics

1992

387

Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: Cast a wide FISHing net!

Donna M. McDonald‐McGinn, Melissa K. Tonnesen, Ayala Laufer‐Cahana,

Genetics in Medicine

2001

314

VEGF: A modifier of the del22q11 (DiGeorge) syndrome?

Ingeborg Stalmans, Diether Lambrechts, Frederik De Smet,

Nature Medicine

2003

310

Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1→q11.2

Mark H. Grossman, Beverly S. Emanuel, Marcia L. Budarf

Genomics

1992

296

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