Jennifer K. Lowe

13.9k total citations · 5 hit papers
48 papers, 5.3k citations indexed

About

Jennifer K. Lowe is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Jennifer K. Lowe has authored 48 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 20 papers in Molecular Biology and 15 papers in Cognitive Neuroscience. Recurrent topics in Jennifer K. Lowe's work include Autism Spectrum Disorder Research (14 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genetic Associations and Epidemiology (9 papers). Jennifer K. Lowe is often cited by papers focused on Autism Spectrum Disorder Research (14 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genetic Associations and Epidemiology (9 papers). Jennifer K. Lowe collaborates with scholars based in United States, United Kingdom and Argentina. Jennifer K. Lowe's co-authors include Daniel H. Geschwind, Steve Horvath, Benjamin J. Blencowe, Rita M. Cantor, Yuan Tian, Irina Voineagu, Xinchen Wang, Jonathan Mill, Patrick G. Johnston and Neelroop Parikshak and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Jennifer K. Lowe

45 papers receiving 5.2k citations

Hit Papers

5 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.

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

2011 1.3k citations Irina Voineagu, Jennifer K. Lowe et al. profile →
Integrative Functional Genomic Analyses Implicate Specific Molecular Pathways and Circuits in Autism

2013 691 citations Neelroop Parikshak, Rui Luo et al. profile →
Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism

2015 542 citations Stanley B. Prusiner, Amanda L. Woerman et al. Proceedings of the National Academy of Sciences profile →
Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism

2016 445 citations Neelroop Parikshak, Virpi Leppä et al. profile →
Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks

2019 257 citations Elizabeth K. Ruzzo, Laura Pérez‐Cano et al. profile →

Peers

Countries citing papers authored by Jennifer K. Lowe

Since Specialization

Citations

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

Fields of papers citing papers by Jennifer K. Lowe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jennifer K. Lowe. 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 Jennifer K. Lowe. The network helps show where Jennifer K. Lowe may publish in the future.

Co-authorship network of co-authors of Jennifer K. Lowe

This figure shows the co-authorship network connecting the top 25 collaborators of Jennifer K. Lowe. A scholar is included among the top collaborators of Jennifer K. Lowe 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 Jennifer K. Lowe. Jennifer K. Lowe 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	Early therapeutic drug monitoring of methotrexate and its association with acute kidney injury: A retrospective cohort study 2024 ·Cancer Medicine ·(unknown), (unknown), Gabriela Villanueva, Ryan Combs, Jennifer K. Lowe, Laura B. Ramsey, (unknown), (unknown), (unknown), (unknown), Carmelo Rizzari, Scott C. Howard	4
2	The contributions of rare inherited and polygenic risk to ASD in multiplex families 2023 ·Proceedings of the National Academy of Sciences ·Matilde Cirnigliaro, Timothy S. Chang, (unknown), Laura Pérez‐Cano, Elizabeth K. Ruzzo, Aaron Gordon, Lucy Bicks, Jae-Yoon Jung, Jennifer K. Lowe, Dennis P. Wall, Daniel H. Geschwind	44
3	What Is Autistic Burnout? A Thematic Analysis of Posts on Two Online Platforms 2021 ·Autism in Adulthood ·(unknown), Amanda L. Richdale, Achini Adikari, Jennifer K. Lowe, Cheryl Dissanayake	70
4	Imaging-genetics of sex differences in ASD: distinct effects of OXTR variants on brain connectivity 2020 ·Translational Psychiatry ·Leanna M. Hernandez, Katherine E. Lawrence, (unknown), (unknown), (unknown), Jennifer K. Lowe, Jeffrey Eilbott, Allison Jack, Elizabeth Aylward, Nadine Gaab, John D. Van Horn, Raphael Bernier, James C. McPartland, Sara Jane Webb, Kevin A. Pelphrey, Shulamite A. Green, Daniel H. Geschwind, Susan Y. Bookheimer, Mirella Dapretto	26
5	ASD restricted and repetitive behaviors associated at 17q21.33: genes prioritized by expression in fetal brains 2017 ·Molecular Psychiatry ·Rita M. Cantor, (unknown), Hyejung Won, Rebecca L. Walker, Jennifer K. Lowe, Daniel H. Geschwind	14
6	Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families 2016 ·The American Journal of Human Genetics ·Virpi Leppä, Stephanie N. Kravitz, Alastair J. Martin, Joris Andrieux, Cédric Le Caignec, Dominique Martin‐Coignard, (unknown), Stephan Sanders, Jennifer K. Lowe, Rita M. Cantor, Daniel H. Geschwind	121
7	Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism breakdown → 2015 ·Proceedings of the National Academy of Sciences ·Stanley B. Prusiner, Amanda L. Woerman, Daniel A. Mordes, Joel C. Watts, Ryan Rampersaud, David B. Berry, Smita S. Patel, Abby Oehler, Jennifer K. Lowe, Stephanie N. Kravitz, Daniel H. Geschwind, David V. Glidden, Glenda M. Halliday, Lefkos Middleton, Steve Gentleman, Lea T. Grinberg, Kurt Giles	542
8	A Quantitative Framework to Evaluate Modeling of Cortical Development by Neural Stem Cells 2014 ·Neuron ·Jason L. Stein, Luis de la Torre-Ubieta, Yuan Tian, Neelroop Parikshak, Israel Hernández, Maria C. Marchetto, (unknown), Daning Lu, Cassidy Hinman, Jennifer K. Lowe, Eric Wexler, Alysson R. Muotri, Fred H. Gage, Kenneth S. Kosik, Daniel H. Geschwind	137
9	Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder 2014 ·Molecular Autism ·Donna M. Werling, Jennifer K. Lowe, Rui Luo, Rita M. Cantor, Daniel H. Geschwind	30
10	Genome-wide Transcriptome Profiling Reveals the Functional Impact of Rare De Novo and Recurrent CNVs in Autism Spectrum Disorders 2012 ·The American Journal of Human Genetics ·Rui Luo, Stephan Sanders, Yuan Tian, Irina Voineagu, Ni Huang, Su H. Chu, Lambertus Klei, Chaochao Cai, Jing Ou, Jennifer K. Lowe, Matthew E. Hurles, Bernie Devlin, Matthew W. State, Daniel H. Geschwind	122
11	Modeling the functional genomics of autism using human neurons 2011 ·Molecular Psychiatry ·Geneviève Konopka, Eric Wexler, Evan D. Rosen, Zohar Mukamel, Gregory E. Osborn, Lu Chen, Daning Lu, Fuying Gao, Kun Gao, Jennifer K. Lowe, Daniel H. Geschwind	65
12	Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population 2010 ·Human Molecular Genetics ·Eimear E. Kenny, (unknown), Alexander Gusev, Jennifer K. Lowe, Jacqueline Salit, J. G. Smith, (unknown), Hyun Min Kang, Christopher Newton‐Cheh, Mark J. Daly, Markus Stoffel, David Altshuler, Jeffrey M. Friedman, Eleazar Eskin, Jan L. Breslow, Itsik Pe’er	19
13	Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult mice 2010 ·Molecular Psychiatry ·Dan Ehninger, Yoshitake Sano, Petrus J. de Vries, Kira A. Dies, David Neal Franz, Dan Geschwind, M Kaur, Yong‐Seok Lee, Weidong Li, Jennifer K. Lowe, Jo Anne Nakagawa, Mustafa Şahin, Kirby D. Smith, Vicky Whittemore, Alcino J. Silva	85
14	Whole population, genome-wide mapping of hidden relatedness 2008 ·Genome Research ·Alexander Gusev, Jennifer K. Lowe, Markus Stoffel, Mark J. Daly, David Altshuler, Jan L. Breslow, Jeffrey M. Friedman, Itsik Pe’er	301
15	Evaluating potential for whole-genome studies in Kosrae, an isolated population in Micronesia 2006 ·Nature Genetics ·Penelope E. Bonnen, Itsik Pe’er, Robert M. Plenge, (unknown), Jennifer K. Lowe, Michael H. Shapero, Richard P. Lifton, Jan L. Breslow, Mark J. Daly, David Reich, Keith Jones, Markus Stoffel, David Altshuler, Jeffrey M. Friedman	52
16	Linkage mapping of the primary disease locus for collie eye anomaly☆ 2003 ·Genomics ·Jennifer K. Lowe, Anna V. Kukekova, Ewen F. Kirkness, (unknown), Geoffrey K. Aguirre, Gregory M. Acland, Elaine A. Ostrander	43
17	Identification of a Mutation Responsible for Hereditary Cone Degeneration in Dog 2002 ·Investigative Ophthalmology & Visual Science ·(unknown), Jennifer K. Lowe, Cathryn S. Mellersh, (unknown), B.S. Milne, David R. Sargan, (unknown), (unknown)	1
18	DNA sequence and physical mapping of the canine transglutaminase 1 gene 2001 ·Cytogenetic and Genome Research ·Kelly M. Credille, Patrick J. Venta, Matthew Breen, Jennifer K. Lowe, Keith E. Murphy, Elaine A. Ostrander, Francis Galibert, Robert W. Dunstan	9
19	Cigars, Slippers and Nightcaps: Attitudes and Actions in "La Regenta" and "Tristana" 1992 ·Anales galdosianos ·Jennifer K. Lowe	2
20	Galdós' use of time in La de Bringas 1980 ·Anales galdosianos ·Jennifer K. Lowe	1

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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