Rosalie Goldberg - Concepedia

Author

Rosalie Goldberg

Albert Einstein College of Medicine

Also Known As

R B Goldberg, R Goldberg, R. Goldberg, Rosalie B Goldberg, Rosalie B. Goldberg, Rosalie Goldberg

Publications

8.8K

Citations

H-Index

Concepts

All Affiliations

Albert Einstein College of Medicine Montefiore Medical Center Yeshiva University University of Geneva St Mary's Hospital

About

Rosalie Goldberg is an author at Albert Einstein College of Medicine specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	16	5.2K
2	Anatomy	3	3	213
3	Language Studies	2	2	604
4	Public Health	2	2	400
5	Arts	1	1	46

Rosalie Goldberg

Publications

Citations

H-Index

Page 1

	Year	Citations
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome Marco Tartaglia, Ernest L. Mehler, Rosalie Goldberg, Nature Genetics Molecular PhysiologySignal TransductionGenetic DisorderReceptor Tyrosine KinaseGenetics	2001	1.7K
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Maria Karayiorgou, Michael A. Morris, Bernice E. Morrow, Proceedings of the National Academy of Sciences Schizophrenia SusceptibilityPsychiatrySchizophrenia Susceptibility GeneGenetic OverlapGenetics	1995	644
A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome. Robert J. Shprintzen, Rosalie Goldberg, Michael L. Lewin, PubMed Congenital Heart AnomalySecondary PalateCongenital DisordersCraniofacial AnomaliesPalate Surgery	1978	598
Psychotic Illness in Patients Diagnosed with Velo-Cardio-Facial Syndrome and Their Relatives Ann E. Pulver, Gerald Nestadt, Rosalie Goldberg, The Journal of Nervous and Mental Disease History Of ScienceComparative LiteraturePsychiatryRaju Ph.dPsychotic Disorder	1994	427
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus Peter Scambler, David A. Kelly, Elizabeth Lindsay, The Lancet Genetic DisorderGeneticsPathologyCongenital Heart DefectDigeorge Locus	1992	418
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 GeneticsGenetic EpidemiologyPathologyMolecular GeneticsCongenital Heart Anomaly	1992	387
Bipolar spectrum disorders in patients diagnosed with velo-cardio- facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder? Demitri F. Papolos, Gianni L. Faedda, Sabine Veit, American Journal of Psychiatry	1996	361
Molecular Definition of 22q11 Deletions in 151 Velo-Cardio-Facial Syndrome Patients Christine Carlson, Howard I. Sirotkin, Raj K. Pandita, The American Journal of Human Genetics	1997	357
Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome Herbert M. Lachman, Bernice E. Morrow, Robert J. Shprintzen, American Journal of Medical Genetics	1996	308
The Velo-Cardio-Facial Syndrome: A Clinical and Genetic Analysis Robert J. Shprintzen, Rosalie Goldberg, D.G. Young, PEDIATRICS	1981	297

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