Barbara Stubblefield

3.5k citations

45 papers · 2.7k indexed · h-index 26

Physiology top 0.5%
Cell Biology top 0.5%
Molecular Biology top 10%
Organic Chemistry top 5%
Neurology top 2%

Co-authors: Ellen Sidransky Nahid Tayebi Edward I. Ginns Brian M. Martin Shoji Tsuji Eduard Orviský Özlem Göker-Alpan Mary E. LaMarca
Topics: Lysosomal Storage Disorders Research (37 papers)Cellular transport and secretion (27 papers)Glycosylation and Glycoproteins Research (14 papers)
Cited by: Cell Biology Physiology Neurology
Journals: Nature New England Journal of Medicine Proceedings of the National Academy of Sciences
Partner nations: United States Israel Czechia

In The Last Decade

Barbara Stubblefield

43 papers receiving 2.6k citations

Peers

Countries citing papers authored by Barbara Stubblefield

Since Specialization

Citations

This map shows the geographic impact of Barbara Stubblefield'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 Barbara Stubblefield with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Barbara Stubblefield more than expected).

Fields of papers citing papers by Barbara Stubblefield

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Barbara Stubblefield. 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 Barbara Stubblefield. The network helps show where Barbara Stubblefield may publish in the future.

Co-authorship network of co-authors of Barbara Stubblefield

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara Stubblefield. A scholar is included among the top collaborators of Barbara Stubblefield 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 Barbara Stubblefield. Barbara Stubblefield 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	A characterization of Gaucher iPS-derived astrocytes: Potential implications for Parkinson's disease 2019 ·Neurobiology of Disease ·Elma Aflaki,Barbara Stubblefield,Ryan P. McGlinchey,Benjamin H. McMahon,Daniel S. Ory,Ellen Sidransky	51
2	Alleles with more than one mutation can complicate genotype/phenotype studies in Mendelian disorders: Lessons from Gaucher disease 2018 ·Molecular Genetics and Metabolism ·Shahzeb Hassan,Grisel Lopez,Barbara Stubblefield,Nahid Tayebi,Ellen Sidransky	7
3	A New Glucocerebrosidase Chaperone Reduces -Synuclein and Glycolipid Levels in iPSC-Derived Dopaminergic Neurons from Patients with Gaucher Disease and Parkinsonism 2016 ·Journal of Neuroscience ·Elma Aflaki,Daniel K. Borger,Nima Moaven,Barbara Stubblefield,Steven A. Rogers,Samarjit Patnaik,Frank J. Schoenen,Wendy Westbroek,Wei Zheng,Patti Sullivan,Hideji Fujiwara,Rohini Sidhu,Zayd M. Khaliq,Grisel Lopez,D. S. Goldstein,Daniel S. Ory,Juan Marugán,Ellen Sidransky	181
4	A mutation in SCARB2 is a modifier in gaucher disease 2011 ·Human Mutation ·Arash Velayati,(unknown),Nidhi Gupta,Jae Hyuk Choi,Nima Moaven,Wendy Westbroek,Özlem Göker-Alpan,Ehud Goldin,Barbara Stubblefield,Edwin H. Kolodny,Nahid Tayebi,Ellen Sidransky	68
5	Aggregation of α-synuclein in brain samples from subjects with glucocerebrosidase mutations 2011 ·Molecular Genetics and Metabolism ·Jae Hyuk Choi,Barbara Stubblefield,Mark Cookson,Ehud Goldin,Arash Velayati,Nahid Tayebi,Ellen Sidransky	61
6	Glucocerebrosidase is present in α-synuclein inclusions in Lewy body disorders 2010 ·Acta Neuropathologica ·Özlem Göker-Alpan,Barbara Stubblefield,Benoit I. Giasson,Ellen Sidransky	144
7	In silico and functional studies of the regulation of the glucocerebrosidase gene 2009 ·Molecular Genetics and Metabolism ·(unknown),Shira G. Ziegler,Kathleen S. Hruska,Barbara Stubblefield,Mary E. LaMarca,Matthew E. Portnoy,Eric D. Green,Ellen Sidransky	11
8	Glucocerebrosidase mutations are not found in association with LRRK2 G2019S in subjects with parkinsonism 2006 ·Neuroscience Letters ·Michael J. Eblan,Sonja W. Scholz,Barbara Stubblefield,Usha Gutti,Özlem Göker-Alpan,Kathleen S. Hruska,Andrew Singleton,Ellen Sidransky	10
9	DNA targeting of rhinal cortex D2 receptor protein reversibly blocks learning of cues that predict reward 2004 ·Proceedings of the National Academy of Sciences ·Zheng Liu,Barry J. Richmond,Elisabeth A. Murray,Richard C. Saunders,(unknown),Barbara Stubblefield,(unknown),Edward I. Ginns	57
10	Myoclonic Epilepsy in Gaucher Disease: Genotype-Phenotype Insights from a Rare Patient Subgroup 2003 ·Pediatric Research ·Joseph K. Park,Eduard Orviský,Nahid Tayebi,Christine R. Kaneski,Mary E. LaMarca,Barbara Stubblefield,Brian M. Martin,Raphael Schiffmann,Ellen Sidransky	71
11	Phosphomannomutase activity in congenital disorders of glycosylation type Ia determined by direct analysis of the interconversion of mannose-1-phosphate to mannose-6-phosphate by high-pH anion-exchange chromatography with pulsed amperometric detection 2003 ·Analytical Biochemistry ·Eduard Orviský,Barbara Stubblefield,R Long,Brian M. Martin,Ellen Sidransky,Donna M. Krasnewich	11
12	The identification of eight novel glucocerebrosidase (GBA) mutations in patients with Gaucher disease 2002 ·Human Mutation ·Eduard Orviský,Joseph K. Park,Adrian G. Parker,Jamie M. Walker,Brian M. Martin,Barbara Stubblefield,Eiichiro Uyama,Nahid Tayebi,Ellen Sidransky	19
13	Type 2 Gaucher Disease with Hydrops Fetalis in an Ashkenazi Jewish Family Resulting from a Novel Recombinant Allele and a Rare Splice Junction Mutation in the Glucocerebrosidase Locus 1998 ·Molecular Genetics and Metabolism ·Kathryn J. Reissner,Nahid Tayebi,Barbara Stubblefield,Vuk Koprivica,Miriam G. Blitzer,Walter M. Holleran,Tina M. Cowan,Shlomo Almashanu,A Maddalena,Evelyn M. Karson,Ellen Sidransky	32
14	Genotypic Heterogeneity and Phenotypic Variation among Patients with Type 2 Gaucher's Disease 1998 ·Pediatric Research ·Nahid Tayebi,Kathryn J. Reissner,Elaine K. Lau,Barbara Stubblefield,(unknown),Brian M. Martin,Ellen Sidransky	51
15	Prenatal lethality of a homozygous null mutation in the human glucocerebrosidase gene 1997 ·American Journal of Medical Genetics ·Nahid Tayebi,(unknown),Wim J. Kleijer,Elaine K. Lau,Patricia Damschroder‐Williams,Barbara Stubblefield,(unknown),Ellen Sidransky	38
16	Animal model of Gaucher's disease from targeted disruption of the mouse glucocerebrosidase gene 1992 ·Nature ·Victor L. J. Tybulewicz,Michel L. Tremblay,(unknown),Rob Willemsen,Barbara Stubblefield,Suzanne L. Winfield,Barbara Zabłocka,Ellen Sidransky,Brian M. Martin,Sing-Ping Huang,Keith A. Mintzer,H Westphal,Richard C. Mulligan,Edward I. Ginns	245
17	Gaudier patients with oculomotor abnormalities do not have a unique genotype 1992 ·Clinical Genetics ·Ellen Sidransky,(unknown),Barbara Stubblefield,(unknown),(unknown),(unknown)	23
18	DNA mutation analysis of Gaucher patients 1992 ·American Journal of Medical Genetics ·Ellen Sidransky,Shoji Tsuji,Brian M. Martin,Barbara Stubblefield,Edward I. Ginns	45
19	Regional Distribution of the GABA_A/Benzodiazepine Receptor (α Subunit) mRNA in Rat Brain 1988 ·Journal of Neurochemistry ·Pascale Montpied,Brian M. Martin,Sandra Cottingham,Barbara Stubblefield,Edward I. Ginns,Steven M. Paul	51
20	Human tyrosine hydroxylase (TH) genomic fragment (pHGTH4) identifies a PstI polymorphism 1988 ·Nucleic Acids Research ·John R. Kelsoe,Barbara Stubblefield,Edward I. Ginns	12

About Barbara Stubblefield

Barbara Stubblefield is a scholar working on Cell Biology, Physiology and Tourism, Leisure and Hospitality Management, having authored 45 papers that have together received 2.7k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (37 papers), Cellular transport and secretion (27 papers) and Glycosylation and Glycoproteins Research (14 papers). The work is most often cited by research in Cell Biology (1.5k citations), Physiology (2.1k citations) and Neurology (580 citations). Barbara Stubblefield has collaborated with scholars based in United States, Israel and Czechia. Frequent co-authors include Ellen Sidransky, Nahid Tayebi, Edward I. Ginns, Brian M. Martin, Shoji Tsuji, Eduard Orviský, Özlem Göker-Alpan, Mary E. LaMarca, Victor Madike and Prabhakara V. Choudary. Their work appears in journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

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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