M. Priscilla Short

7.3k citations

55 papers · 4.2k indexed · h-index 34

Molecular Biology top 5%
Genetics top 1%
Physiology top 2%
Neurology top 1%
Cellular and Molecular Neuroscience top 5%

Co-authors: X. O. Breakefield Elizabeth P. Henske David J. Kwiatkowski D J Kwiatkowski Xandra O. Breakefield Ole Isacson Mia MacCollin David Kronn
Topics: Tuberous Sclerosis Complex Research (14 papers)Neurofibromatosis and Schwannoma Cases (10 papers)Virus-based gene therapy research (8 papers)
Cited by: Developmental Neuroscience Neurology Physiology
Journals: New England Journal of Medicine Journal of Clinical Investigation Nature Genetics
Partner nations: United States United Kingdom Canada

In The Last Decade

M. Priscilla Short

55 papers receiving 4.1k citations

Peers

Countries citing papers authored by M. Priscilla Short

Since Specialization

Citations

This map shows the geographic impact of M. Priscilla Short's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by M. Priscilla Short with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Priscilla Short more than expected).

Fields of papers citing papers by M. Priscilla Short

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Priscilla Short. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by M. Priscilla Short. The network helps show where M. Priscilla Short may publish in the future.

Co-authorship network of co-authors of M. Priscilla Short

This figure shows the co-authorship network connecting the top 25 collaborators of M. Priscilla Short. A scholar is included among the top collaborators of M. Priscilla Short based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with M. Priscilla Short. M. Priscilla Short is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	IMPOWER: a national patient-generated registry for intestinal malrotation exploring diagnosis, treatment, and surgical outcomes 2023 ·Orphanet Journal of Rare Diseases ·(unknown),Scott C. Fligor,Savas T. Tsikis,M. Priscilla Short,Katie E. Corcoran,Amy Rogers,Kathleen M. Gura,Mark Puder	1
2	The physician’s role in discussing organ donation with families* 2003 ·Critical Care Medicine ·Michael A. Williams,Pamela A. Lipsett,Cynda Hylton Rushton,Eugene C. Grochowski,Ivor Berkowitz,(unknown),John Shatzer,M. Priscilla Short,Myron Genel	98
3	Descriptive analysis of tibial pseudarthrosis in patients with neurofibromatosis 1 1999 ·American Journal of Medical Genetics ·David A. Stevenson,Patricia Birch,Jan M. Friedman,David Viskochil,P Balestrazzi,Stefania Boni,Annegret Buske,Bruce R. Korf,Michihito Niimura,Enikö K. Pivnick,Elizabeth K. Schorry,M. Priscilla Short,Romano Tenconi,James H. Tonsgard,John C. Carey	96
4	Human XPMC2H: cDNA Cloning, Mapping to 9q34, Genomic Structure, and Evaluation as TSC1 1997 ·Genomics ·J. Kwiatkowska,Ryszard Słomski,Sergiusz Jóźwiak,M. Priscilla Short,David J. Kwiatkowski	4
5	Human Fetal Astrocytes as an Ex Vivo Gene Therapy Vehicle for Delivering Biologically Active Nerve Growth Factor 1997 ·Human Gene Therapy ·Qing Lin,Lee Anna Cunningham,Leon G. Epstein,Peter Pecháň,M. Priscilla Short,Christina Fleet,Martha C. Bohn	22
6	Molecular Analysis of the NF2 Tumor-Suppressor Gene in Schwannomatosis 1997 ·The American Journal of Human Genetics ·Lee B. Jacoby,(unknown),Kevin Davis,David Kronn,M. Priscilla Short,James F. Gusella,Mia MacCollin	122
7	Novel Mutations Detected in the TSC2 Hene From Both Sporadic and Familial TSC Patients 1996 ·Human Molecular Genetics ·Peter J. Wilson,Vijaya Ramesh,Arthur G. Kristiansen,Catherine Bove,Sergiusz Jóźwiak,David J. Kwiatkowski,M. Priscilla Short,Jonathan L. Haines	67
8	Clinical, Neuropathological and Genetic Aspects of the Tuberous Sclerosis Complex 1995 ·Brain Pathology ·M. Priscilla Short,Edward P. Richardson,Jonathan L. Haines,David J. Kwiatkowski	40
9	Identification of VAV2 on 9q34 and its exclusion as the tuberous sclerosis gene TSC1 1995 ·Annals of Human Genetics ·Elizabeth P. Henske,M. Priscilla Short,Sergiusz Jóźwiak,(unknown),(unknown),(unknown),David J. Kwiatkowski	73
10	Loss of heterozygosity in the tuberous sclerosis (TSC2) region of chromosome band l6p13 occurs in sporadic as well as TSC‐associated renal angiomyolipomas 1995 ·Genes Chromosomes and Cancer ·Elizabeth P. Henske,Hartmut P.H. Neumann,Bernd W. Scheithauer,Eberhard W. Herbst,M. Priscilla Short,David J. Kwiatkowski	210
11	Identification of VAV2 on 9q34 and its exclusion as the tuberous sclerosis gene TSC1 1994 ·The American Journal of Human Genetics ·(unknown),M. Priscilla Short,Sergiusz Jóźwiak	1
12	Intramedullary hemorrhage in spinal cord hemangioblastoma 1994 ·Journal of neurosurgery ·John S. Yu,M. Priscilla Short,J. D. Schumacher,Paul H. Chapman,(unknown)	40
13	Effects of biologically delivered NGF, BDNF and bFGF on striatal excitotoxic lesions 1993 ·Neuroreport ·David M. Frim,(unknown),M. Priscilla Short,(unknown),Michael Klagsbrun,X. O. Breakefield,Ole Isacson	151
14	Transplantation of a Polymer-Encapsulated Cell Line Genetically Engineered to Release NGF 1993 ·Experimental Neurology ·(unknown),Xandra O. Breakefield,M. Priscilla Short,Patrick Aebischer	100
15	Local protective effects of nerve growth factor-secreting fibroblasts against excitotoxic lesions in the rat striatum 1993 ·Journal of neurosurgery ·David M. Frim,M. Priscilla Short,William S. Rosenberg,Joseph R. Simpson,X. O. Breakefield,Ole Isacson	83
16	Gene therapy of maliganant brain tumors: A rat glioma line bearing the herpes simplex virus type 1‐thymidine kinase gene and wild type retrovirus kills other tumor cells 1992 ·Journal of Neuroscience Research ·(unknown),M. Priscilla Short,(unknown),F. L. Moolten,X. O. Breakefield,R L Martuza	141
17	Selective killing of glioma cells in culture and in vivo by retrovirus transfer of the herpes simplex virus thymidine kinase gene. 1991 ·PubMed ·(unknown),R L Martuza,Doros Platika,M. Priscilla Short,Amy Malick,(unknown),X. O. Breakefield	170
18	An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two‐Point Methods^a 1991 ·Annals of the New York Academy of Sciences ·Sue Povey,(unknown),(unknown),Mari‐Wyn Burley,M. Smith,Pamela Flodman,N.E. Morton,J. H. Edwards,Julian R. Sampson,John R.W. Yates,J. L. Haines,J. Amos,M. Priscilla Short,L. A. Sandkuyl,D. J. J. Halley,Alan Fryer,(unknown),Rolf Mueller,(unknown),M Super,(unknown)	16
19	Clinical Findings and Linkage Studies in Familial Tuberous Sclerosis 1991 ·Annals of the New York Academy of Sciences ·M. Priscilla Short,Jess Haines,Ann Jewell,Bassem A. Bejjani,(unknown),(unknown),H MacFarlane,E. Andermann,(unknown),J. Amos	2
20	Autocrine Differentiation of PC12 Cells Mediated by Retroviral Vectors 1990 ·Developmental Neuroscience ·M. Priscilla Short,Michael B. Rosenberg,(unknown),Fred H. Gage,T Friedmann,X. O. Breakefield	24

About M. Priscilla Short

M. Priscilla Short is a scholar working on Developmental Neuroscience, Neurology and Physiology, having authored 55 papers that have together received 4.2k indexed citations. Recurring topics across this work include Tuberous Sclerosis Complex Research (14 papers), Neurofibromatosis and Schwannoma Cases (10 papers) and Virus-based gene therapy research (8 papers). The work is most often cited by research in Developmental Neuroscience (292 citations), Neurology (877 citations) and Physiology (1.1k citations). M. Priscilla Short has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include X. O. Breakefield, Elizabeth P. Henske, David J. Kwiatkowski, D J Kwiatkowski, Xandra O. Breakefield, Ole Isacson, Mia MacCollin, David Kronn, James H. Tonsgard and Amy Malick. Their work appears in journals such as New England Journal of Medicine, Journal of Clinical Investigation and Nature Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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