Barbara Antalffy

5.7k total citations · 3 hit papers
25 papers, 4.5k citations indexed

About

Barbara Antalffy is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Barbara Antalffy has authored 25 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 10 papers in Genetics. Recurrent topics in Barbara Antalffy's work include Genetics and Neurodevelopmental Disorders (8 papers), Mitochondrial Function and Pathology (6 papers) and Genetic Neurodegenerative Diseases (6 papers). Barbara Antalffy is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Mitochondrial Function and Pathology (6 papers) and Genetic Neurodegenerative Diseases (6 papers). Barbara Antalffy collaborates with scholars based in United States, Japan and Italy. Barbara Antalffy's co-authors include Huda Y. Zoghbi, Harry T. Orr, Dawna Armstrong, Christopher J. Cummings, Arthur L. Beaudet, Donald Defranco, Michael A. Mancini, Richard Paylor, Lisa A. Yuva‐Paylor and Dawna L. Armstrong and has published in prestigious journals such as Neuron, Nature Genetics and Journal of Neuroscience.

In The Last Decade

Barbara Antalffy

25 papers receiving 4.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1

1998 635 citations Christopher J. Cummings, Michael A. Mancini et al. Nature Genetics profile →
Mice with Truncated MeCP2 Recapitulate Many Rett Syndrome Features and Display Hyperacetylation of Histone H3

2002 605 citations Mona D. Shahbazian, Juan I. Young et al. Neuron profile →
Mutation of the E6-AP Ubiquitin Ligase Reduces Nuclear Inclusion Frequency While Accelerating Polyglutamine-Induced Pathology in SCA1 Mice

1999 409 citations Christopher J. Cummings, Yaling Sun et al. Neuron profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Barbara Antalffy United States	21	3.2k	2.0k	1.9k	941	448	25	4.5k
Dawna Armstrong United States	20	3.0k 0.9×	863 0.4×	2.1k 1.1×	793 0.8×	214 0.5×	33	4.2k
Vincent des Portes France	30	2.2k 0.7×	780 0.4×	2.1k 1.1×	881 0.9×	164 0.4×	91	4.1k
Jamel Chelly France	38	3.3k 1.0×	955 0.5×	3.3k 1.8×	1.0k 1.1×	113 0.3×	110	5.3k
Martin L. Doughty United States	16	2.0k 0.6×	1.7k 0.9×	452 0.2×	585 0.6×	235 0.5×	31	3.6k
R. Frank Kooy Belgium	44	4.0k 1.2×	1.2k 0.6×	4.8k 2.6×	2.5k 2.7×	112 0.3×	170	6.8k
Justin R. Fallon United States	36	3.2k 1.0×	1.9k 1.0×	718 0.4×	413 0.4×	171 0.4×	61	4.6k
X. William Yang United States	38	3.8k 1.2×	3.1k 1.6×	613 0.3×	428 0.5×	1.1k 2.5×	68	5.7k
Janice R. Naegele United States	30	1.8k 0.6×	1.3k 0.7×	435 0.2×	492 0.5×	137 0.3×	64	3.0k
Kathie M. Bishop United States	25	2.6k 0.8×	1.1k 0.5×	648 0.3×	346 0.4×	654 1.5×	53	4.2k
Didier Devys France	32	7.0k 2.2×	3.7k 1.8×	2.7k 1.5×	1.2k 1.3×	1.3k 3.0×	60	8.5k

Countries citing papers authored by Barbara Antalffy

Since Specialization

Citations

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

Fields of papers citing papers by Barbara Antalffy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Antalffy

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara Antalffy. A scholar is included among the top collaborators of Barbara Antalffy 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 Antalffy. Barbara Antalffy 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

Bi, Weimin, Jiong Yan, Lisa A. Yuva‐Paylor, et al.. (2007). Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes. Human Molecular Genetics. 16(15). 1802–1813. 65 indexed citations

Li, Xiaoxin, Qingyao Shu, Jack M. Su, et al.. (2007). Differential expression of survivin splice isoforms in medulloblastomas. Neuropathology and Applied Neurobiology. 33(1). 67–76. 15 indexed citations

Shroyer, Noah F., et al.. (2007). Intestine-Specific Ablation of Mouse atonal homolog 1 (Math1) Reveals a Role in Cellular Homeostasis. Gastroenterology. 132(7). 2478–2488. 240 indexed citations

Dindot, Scott V., Barbara Antalffy, M Bhattacharjee, & Arthur L. Beaudet. (2007). The Angelman syndrome ubiquitin ligase localizes to the synapse and nucleus, and maternal deficiency results in abnormal dendritic spine morphology. Human Molecular Genetics. 17(1). 111–118. 316 indexed citations

Shroyer, Noah F., et al.. (2007). WITHDRAWN: Intestine specific ablation of mouse atonal homolog 1 (Math1) reveals a role in cellular homeostasis.. Gastroenterology. 1 indexed citations

Moretti, Paolo, Jonathan M. Levenson, Fortunato Battaglia, et al.. (2006). Learning and Memory and Synaptic Plasticity Are Impaired in a Mouse Model of Rett Syndrome. Journal of Neuroscience. 26(1). 319–327. 427 indexed citations

Lorenzetti, Diego, Barbara Antalffy, Hannes Vogel, et al.. (2004). The neurological mutant quaking viable is Parkin deficient. Mammalian Genome. 15(3). 210–217. 38 indexed citations

Su, Jack M., László Perlaky, Xiaonan Li, et al.. (2004). Comparison of Ethanol Versus Formalin Fixation on Preservation of Histology and RNA in Laser Capture Microdissected Brain Tissues. Brain Pathology. 14(2). 175–182. 50 indexed citations

Assadi, Amir H., Guangcheng Zhang, Uwe Beffert, et al.. (2003). Interaction of reelin signaling and Lis1 in brain development. Nature Genetics. 35(3). 270–276. 171 indexed citations

10.

Watase, Kei, Edwin J. Weeber, Bisong Xu, et al.. (2002). A Long CAG Repeat in the Mouse Sca1 Locus Replicates SCA1 Features and Reveals the Impact of Protein Solubility on Selective Neurodegeneration. Neuron. 34(6). 905–919. 263 indexed citations

11.

Shahbazian, Mona D., Juan I. Young, Lisa A. Yuva‐Paylor, et al.. (2002). Mice with Truncated MeCP2 Recapitulate Many Rett Syndrome Features and Display Hyperacetylation of Histone H3. Neuron. 35(2). 243–254. 605 indexed citations breakdown →

12.

Deguchi, Kimiko, Christine Reyes, Subhendu Chakraborty, et al.. (2001). Substance P immunoreactivity in the enteric nervous system in Rett syndrome. Brain and Development. 23. S127–S132. 8 indexed citations

13.

Hannay, H. Julia, et al.. (2001). Spatial learning deficits without hippocampal neuronal loss in a model of early-onset epilepsy. Neuroscience. 107(1). 71–84. 62 indexed citations

14.

Lin, Xi, Barbara Antalffy, Dongcheul Kang, Harry T. Orr, & Huda Y. Zoghbi. (2000). Polyglutamine expansion down-regulates specific neuronal genes before pathologic changes in SCA1. Nature Neuroscience. 3(2). 157–163. 294 indexed citations

15.

Anderson, Anne E., Richard A. Hrachovy, Barbara Antalffy, Don Armstrong, & John W. Swann. (1999). A chronic focal epilepsy with mossy fiber sprouting follows recurrent seizures induced by intrahippocampal tetanus toxin injection in infant rats. Neuroscience. 92(1). 73–82. 42 indexed citations

16.

Armstrong, Dawna D., Kay Dunn, & Barbara Antalffy. (1998). Decreased Dendritic Branching in Frontal, Motor and Limbic Cortex in Rett Syndrome Compared with Trisomy 21. Journal of Neuropathology & Experimental Neurology. 57(11). 1013–1017. 102 indexed citations

17.

Cummings, Christopher J., Michael A. Mancini, Barbara Antalffy, et al.. (1998). Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1. Nature Genetics. 19(2). 148–154. 635 indexed citations breakdown →

18.

Clark, Gary, et al.. (1997). Predominant Localization of the LIS Family of Gene Products to Cajal-Retzius Cells and Ventricular Neuroepithelium in the Developing Human Cortex. Journal of Neuropathology & Experimental Neurology. 56(9). 1044–1052. 40 indexed citations

19.

Armstrong, Dawna, et al.. (1995). Selective Dendritic Alterations in the Cortex of Rett Syndrome. Journal of Neuropathology & Experimental Neurology. 54(2). 195–201. 292 indexed citations

20.

Servadio, Antonio, Beena Koshy, Dawna Armstrong, et al.. (1995). Expression analysis of the ataxin–1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals. Nature Genetics. 10(1). 94–98. 240 indexed citations

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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