Denise Levitch

1.7k total citations
8 papers, 766 citations indexed

About

Denise Levitch is a scholar working on Physiology, Neurology and Molecular Biology. According to data from OpenAlex, Denise Levitch has authored 8 papers receiving a total of 766 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Physiology, 4 papers in Neurology and 3 papers in Molecular Biology. Recurrent topics in Denise Levitch's work include Alzheimer's disease research and treatments (6 papers), Amyotrophic Lateral Sclerosis Research (4 papers) and Genomics and Rare Diseases (2 papers). Denise Levitch is often cited by papers focused on Alzheimer's disease research and treatments (6 papers), Amyotrophic Lateral Sclerosis Research (4 papers) and Genomics and Rare Diseases (2 papers). Denise Levitch collaborates with scholars based in United States, Australia and Chile. Denise Levitch's co-authors include Alison Goate, Joanne Norton, John C. Morris, Nigel J. Cairns, Sumi Chakraverty, Michael A. Gitcho, Kimmo J. Hatanpaa, Charles L. White, Eileen H. Bigio and Matt Baker and has published in prestigious journals such as Neurology, Annals of Neurology and Human Mutation.

In The Last Decade

Denise Levitch

8 papers receiving 753 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Denise Levitch United States	6	635	302	264	226	161	8	766
P. M. Andersen Sweden	7	649 1.0×	318 1.1×	227 0.9×	221 1.0×	206 1.3×	9	804
William Camu France	12	787 1.2×	416 1.4×	293 1.1×	152 0.7×	217 1.3×	16	957
Rubika Balendra United Kingdom	9	607 1.0×	331 1.1×	354 1.3×	130 0.6×	88 0.5×	16	837
Geert Joris Belgium	8	755 1.2×	364 1.2×	319 1.2×	256 1.1×	189 1.2×	11	926
Anissa Fergani France	10	635 1.0×	373 1.2×	271 1.0×	141 0.6×	85 0.5×	10	843
Sandra Pereson Belgium	5	545 0.9×	267 0.9×	236 0.9×	171 0.8×	118 0.7×	6	662
Corinna Hendrich Germany	8	525 0.8×	225 0.7×	157 0.6×	206 0.9×	117 0.7×	10	665
I. R. A. Mackenzie Canada	3	785 1.2×	260 0.9×	320 1.2×	366 1.6×	245 1.5×	5	934
Jenna M. Gregory United Kingdom	15	474 0.7×	229 0.8×	346 1.3×	153 0.7×	113 0.7×	38	739
P. Corcia France	9	514 0.8×	300 1.0×	165 0.6×	91 0.4×	79 0.5×	12	606

Countries citing papers authored by Denise Levitch

Since Specialization

Citations

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

Fields of papers citing papers by Denise Levitch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Denise Levitch

This figure shows the co-authorship network connecting the top 25 collaborators of Denise Levitch. A scholar is included among the top collaborators of Denise Levitch 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 Denise Levitch. Denise Levitch is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

1.

Karch, Celeste M., Damián Hernández, Jen‐Chyong Wang, et al.. (2018). Human fibroblast and stem cell resource from the Dominantly Inherited Alzheimer Network. Alzheimer s Research & Therapy. 10(1). 69–69. 23 indexed citations

2.

Hsu, Simon, Brian A. Gordon, Russ C. Hornbeck, et al.. (2018). Discovery and validation of autosomal dominant Alzheimer’s disease mutations. Alzheimer s Research & Therapy. 10(1). 67–67. 27 indexed citations

3.

Ravenscroft, Thomas A., Cyril Pottier, Melissa E. Murray, et al.. (2016). The presenilin 1 p.Gly206Ala mutation is a frequent cause of early-onset Alzheimer's disease in Hispanics in Florida.. PubMed. 5(1). 94–101. 5 indexed citations

4.

Norton, Joanne, N.J. Cairns, Sumitra Chakraverty, et al.. (2009). PRESENILIN1 G217R MUTATION LINKED TO ALZHEIMER DISEASE WITH COTTON WOOL PLAQUES. Neurology. 73(6). 480–482. 7 indexed citations

5.

Gitcho, Michael A., Robert H. Baloh, Sumi Chakraverty, et al.. (2008). TDP‐43 A315T mutation in familial motor neuron disease. Annals of Neurology. 63(4). 535–538. 496 indexed citations

6.

Mukherjee, Odity, Jun Wang, Michael A. Gitcho, et al.. (2008). Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia. Human Mutation. 29(4). 512–521. 63 indexed citations

7.

Gitcho, Michael A., Robert H. Baloh, Sumi Chakraverty, et al.. (2008). P3‐287: TDP‐43 A315T mutation in familial motor neuron disease. Alzheimer s & Dementia. 4(4S_Part_18). 1 indexed citations

8.

Mukherjee, Odity, Pau Pástor, Nigel J. Cairns, et al.. (2006). HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin‐positive, tau‐negative inclusions caused by a missense mutation in the signal peptide of progranulin. Annals of Neurology. 60(3). 314–322. 144 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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