Lauren Snider

5.9k total citations · 3 hit papers
33 papers, 4.7k citations indexed

About

Lauren Snider is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Lauren Snider has authored 33 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 7 papers in Physiology and 7 papers in Genetics. Recurrent topics in Lauren Snider's work include Muscle Physiology and Disorders (19 papers), RNA Research and Splicing (12 papers) and RNA modifications and cancer (5 papers). Lauren Snider is often cited by papers focused on Muscle Physiology and Disorders (19 papers), RNA Research and Splicing (12 papers) and RNA modifications and cancer (5 papers). Lauren Snider collaborates with scholars based in United States, Netherlands and South Africa. Lauren Snider's co-authors include Stephen J. Tapscott, H Weintraub, Silvère M. van der Maarel, Rabi Tawil, Ralph A.W. Rupp, Stanley M. Hollenberg, Harold Weintraub, Richard J.L.F. Lemmers, Linda N. Geng and Daniel G. Miller and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Lauren Snider

33 papers receiving 4.6k 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.

Conversion of Xenopus Ectoderm into Neurons by NeuroD, a Basic Helix-Loop-Helix Protein

1995 892 citations Stanley M. Hollenberg, Lauren Snider et al. Science profile →
Xenopus embryos regulate the nuclear localization of XMyoD.

1994 566 citations Lauren Snider, H Weintraub et al. profile →
A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy

2010 528 citations Richard J.L.F. Lemmers, Patrick J. van der Vliet et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lauren Snider United States	23	4.1k	762	730	569	533	33	4.7k
Shannon J. Odelberg United States	26	2.2k 0.5×	506 0.7×	751 1.0×	222 0.4×	166 0.3×	49	3.8k
Scott Q. Harper United States	27	3.9k 0.9×	1.1k 1.5×	1.1k 1.5×	413 0.7×	540 1.0×	54	4.4k
Eva Bober Germany	36	5.1k 1.2×	899 1.2×	301 0.4×	465 0.8×	571 1.1×	64	6.3k
Jeh-Ping Liu United States	16	4.1k 1.0×	1.3k 1.7×	1.1k 1.5×	226 0.4×	255 0.5×	20	6.5k
Vincenzo Nigro Italy	43	5.7k 1.4×	1.5k 2.0×	1.3k 1.8×	659 1.2×	1.3k 2.5×	224	7.1k
Bettina Erdmann Germany	26	3.0k 0.7×	410 0.5×	496 0.7×	165 0.3×	864 1.6×	47	4.6k
Christophe Marcelle France	32	3.6k 0.9×	873 1.1×	500 0.7×	468 0.8×	70 0.1×	62	4.4k
Ronald A. Conlon United States	31	4.9k 1.2×	1.0k 1.3×	710 1.0×	256 0.4×	121 0.2×	45	6.1k
G. Giacomo Consalez Italy	35	2.0k 0.5×	667 0.9×	723 1.0×	154 0.3×	176 0.3×	93	3.3k
Jean‐Philippe Hugnot France	28	2.6k 0.6×	263 0.3×	655 0.9×	285 0.5×	499 0.9×	62	3.4k

Countries citing papers authored by Lauren Snider

Since Specialization

Citations

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

Fields of papers citing papers by Lauren Snider

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lauren Snider

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

Wong, Chao-Jen, Seth D. Friedman, Lauren Snider, et al.. (2024). Regional and bilateral MRI and gene signatures in facioscapulohumeral dystrophy: implications for clinical trial design and mechanisms of disease progression. Human Molecular Genetics. 33(8). 698–708. 10 indexed citations

Campbell, Amy E., Matthew Yates, Jun Zhong, et al.. (2017). BET bromodomain inhibitors and agonists of the beta-2 adrenergic receptor identified in screens for compounds that inhibit DUX4 expression in FSHD muscle cells. Skeletal Muscle. 7(1). 16–16. 51 indexed citations

Snider, Lauren, Zizhen Yao, Rabi Tawil, et al.. (2015). DICER/AGO-dependent epigenetic silencing of D4Z4 repeats enhanced by exogenous siRNA suggests mechanisms and therapies for FSHD. Human Molecular Genetics. 24(17). 4817–4828. 40 indexed citations

Feng, Qing, Lauren Snider, Sujatha Jagannathan, et al.. (2015). A feedback loop between nonsense-mediated decay and the retrogene DUX4 in facioscapulohumeral muscular dystrophy. eLife. 4. 98 indexed citations

Yao, Zizhen, Lauren Snider, Judit Balog, et al.. (2014). DUX4-induced gene expression is the major molecular signature in FSHD skeletal muscle. Human Molecular Genetics. 23(20). 5342–5352. 161 indexed citations

Young, Janet M., Zizhen Yao, Lauren Snider, et al.. (2013). DUX4 Binding to Retroelements Creates Promoters That Are Active in FSHD Muscle and Testis. PLoS Genetics. 9(11). e1003947–e1003947. 128 indexed citations

Parker, Maura H., Carol Loretz, Ashlee E. Tyler, et al.. (2012). Inhibition of CD26/DPP-IV enhances donor muscle cell engraftment and stimulates sustained donor cell proliferation. Skeletal Muscle. 2(1). 4–4. 9 indexed citations

Geng, Linda N., Zizhen Yao, Lauren Snider, et al.. (2011). DUX4 Activates Germline Genes, Retroelements, and Immune Mediators: Implications for Facioscapulohumeral Dystrophy. Developmental Cell. 22(1). 38–51. 339 indexed citations

Lemmers, Richard J.L.F., Patrick J. van der Vliet, Rinse Klooster, et al.. (2010). A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy. Science. 329(5999). 1650–1653. 528 indexed citations breakdown →

10.

Snider, Lauren, Linda N. Geng, Richard J.L.F. Lemmers, et al.. (2010). Facioscapulohumeral Dystrophy: Incomplete Suppression of a Retrotransposed Gene. PLoS Genetics. 6(10). e1001181–e1001181. 364 indexed citations

11.

Snider, Lauren, Ashlee E. Tyler, Linda N. Geng, et al.. (2009). RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy. Human Molecular Genetics. 18(13). 2414–2430. 167 indexed citations

12.

Snider, Lauren & Stephen J. Tapscott. (2003). Emerging Parallels in the Generation and Regeneration of Skeletal Muscle. Cell. 113(7). 811–812. 26 indexed citations

13.

Olson, James M., Atsushi Asakura, Lauren Snider, et al.. (2001). NeuroD2 Is Necessary for Development and Survival of Central Nervous System Neurons. Developmental Biology. 234(1). 174–187. 121 indexed citations

14.

Klesert, Todd R., John I. Clark, James Maylie, et al.. (2000). Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy. Nature Genetics. 25(1). 105–109. 182 indexed citations

15.

Kraut, Norbert, et al.. (1998). Requirement of the mouse I-mfa gene for placental development and skeletal patterning. The EMBO Journal. 17(21). 6276–6288. 95 indexed citations

16.

McCormick, Mary, Rulla M. Tamimi, Lauren Snider, et al.. (1996). neuroD2 and neuroD3 : Distinct Expression Patterns and Transcriptional Activation Potentials within the neuroD Gene Family. Molecular and Cellular Biology. 16(10). 5792–5800. 144 indexed citations

17.

Laue, Thomas M., Melissa A. Starovasnik, H Weintraub, et al.. (1995). MyoD forms micelles which can dissociate to form heterodimers with E47: implications of micellization on function.. Proceedings of the National Academy of Sciences. 92(25). 11824–11828. 12 indexed citations

18.

Hollenberg, Stanley M., et al.. (1995). Conversion of Xenopus Ectoderm into Neurons by NeuroD, a Basic Helix-Loop-Helix Protein. Science. 268(5212). 836–844. 892 indexed citations breakdown →

19.

Snider, Lauren, et al.. (1992). Maturation of mouse mammary tumor virus envelope protein is blocked by a specific point mutation. Virology. 189(1). 393–396. 1 indexed citations

20.

Snider, Lauren, Janis L. Corey, Sridhar K. Rabindran, & Michael R. Stallcup. (1990). Characterization of Oligosaccharide Chains on Mouse Mammary Tumor Virus Envelope Proteins and the Implications for the Mechanism of Their Glucocorticoid Regulated Processing. Molecular Endocrinology. 4(5). 749–757. 11 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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