Jennifer Howe

11.0k total citations
38 papers, 876 citations indexed

About

Jennifer Howe is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Jennifer Howe has authored 38 papers receiving a total of 876 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 19 papers in Cognitive Neuroscience and 10 papers in Molecular Biology. Recurrent topics in Jennifer Howe's work include Autism Spectrum Disorder Research (18 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Genomic variations and chromosomal abnormalities (10 papers). Jennifer Howe is often cited by papers focused on Autism Spectrum Disorder Research (18 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Genomic variations and chromosomal abnormalities (10 papers). Jennifer Howe collaborates with scholars based in Canada, United States and United Kingdom. Jennifer Howe's co-authors include Stephen W. Scherer, Péter Szatmári, Christian R. Marshall, Volker Endris, Angelika Rieß, Birgit Weiß, Rolf Sprengel, Michael Bonin, Simone Berkel and Dalila Pinto and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and PLoS ONE.

In The Last Decade

Jennifer Howe

34 papers receiving 847 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jennifer Howe Canada 13 456 362 331 118 87 38 876
Aaron R. Jeffries United Kingdom 20 564 1.2× 838 2.3× 204 0.6× 108 0.9× 59 0.7× 48 1.3k
Katy Phelan United States 12 622 1.4× 562 1.6× 312 0.9× 75 0.6× 74 0.9× 32 995
Alex Plocik United States 11 223 0.5× 800 2.2× 91 0.3× 88 0.7× 170 2.0× 14 1.2k
Giuseppe LaFauci United States 17 370 0.8× 598 1.7× 224 0.7× 32 0.3× 21 0.2× 23 875
Mark N. Ziats United States 16 409 0.9× 617 1.7× 352 1.1× 91 0.8× 23 0.3× 20 1.1k
Karl J. Fryxell United States 16 196 0.4× 651 1.8× 97 0.3× 251 2.1× 109 1.3× 22 1.1k
Alicia Guemez‐Gamboa United States 13 370 0.8× 472 1.3× 267 0.8× 165 1.4× 17 0.2× 19 1.0k
Michal Bronstein Israel 10 280 0.6× 334 0.9× 72 0.2× 56 0.5× 22 0.3× 11 767
Ayumi Matsumoto Japan 15 156 0.3× 221 0.6× 76 0.2× 70 0.6× 136 1.6× 61 727

Countries citing papers authored by Jennifer Howe

Since Specialization
Citations

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

Fields of papers citing papers by Jennifer Howe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jennifer Howe

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

All Works

20 of 20 papers shown
1.
Sundberg, Maria, Carole Shum, Nina R. Makhortova, et al.. (2025). Human iPSC-derived glutamatergic neurons with pathogenic KCNQ2 variants display hyperactive bursting phenotypes. Neurobiology of Disease. 216. 107126–107126.
2.
Hoang, Ny, Jennifer Howe, Alana Iaboni, et al.. (2025). Clinical utility of genome sequencing in autism: illustrative examples from a genomic research study. Journal of Medical Genetics. 62(6). 413–421. 1 indexed citations
3.
4.
Eisfeldt, Jesper, Edward J. Higginbotham, Jennifer Howe, et al.. (2024). Resolving complex duplication variants in autism spectrum disorder using long-read genome sequencing. Genome Research. 34(11). 1763–1773. 3 indexed citations
5.
Shum, Carole, Bhooma Thiruvahindrapuram, Zhuozhi Wang, et al.. (2023). Combining Off‐flow, a Nextflow‐coded program, and whole genome sequencing reveals unintended genetic variation in CRISPR/Cas-edited iPSCs. Computational and Structural Biotechnology Journal. 23. 638–647. 2 indexed citations
6.
Faheem, Muhammad, Éric Deneault, Roumiana Alexandrova, et al.. (2023). Disruption of DDX53 coding sequence has limited impact on iPSC-derived human NGN2 neurons. BMC Medical Genomics. 16(1). 5–5. 4 indexed citations
7.
Woodbury‐Smith, Marc, Lia D’Abate, Dimitri J. Stavropoulos, et al.. (2023). The Phenotypic variability of 16p11.2 distal BP2–BP3 deletion in a transgenerational family and in neurodevelopmentally ascertained samples. Journal of Medical Genetics. 60(12). 1153–1160. 1 indexed citations
8.
Moreira, Danielle de Paula, Isaac E. García, Francisco Aboitiz, et al.. (2022). Mutations in trpγ, the homologue of TRPC6 autism candidate gene, causes autism-like behavioral deficits in Drosophila. Molecular Psychiatry. 27(8). 3328–3342. 12 indexed citations
9.
Cheng, Zhiliang, Kevin D. O’Brien, Jennifer Howe, et al.. (2022). INZ‐701, a recombinant ENPP1 enzyme, prevents ectopic calcification in an Abcc6−/− mouse model of pseudoxanthoma elasticum. Experimental Dermatology. 31(7). 1095–1101. 13 indexed citations
10.
Parmalee, Nancy L., Kiran Kaur, Jennifer Howe, et al.. (2022). Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants. npj Genomic Medicine. 7(1). 13–13. 20 indexed citations
11.
Sangster, Kevin T., Jennifer Kao, Mehdi Zarrei, et al.. (2022). Regionally defined proteomic profiles of human cerebral tissue and organoids reveal conserved molecular modules of neurodevelopment. Cell Reports. 39(8). 110846–110846. 6 indexed citations
12.
Bankapur, Asma, Ibrahim M. Inuwa, Mehdi Zarrei, et al.. (2021). Single-cell transcriptome identifies molecular subtype of autism spectrum disorder impacted by de novo loss-of-function variants regulating glial cells. Human Genomics. 15(1). 68–68. 21 indexed citations
13.
Cheng, Zhiliang, Kevin D. O’Brien, Jennifer Howe, et al.. (2020). INZ-701 Prevents Ectopic Tissue Calcification and Restores Bone Architecture and Growth in ENPP1-Deficient Mice. Journal of Bone and Mineral Research. 36(8). 1594–1604. 25 indexed citations
14.
Yusuf, Afiqah, Tal Savion‐Lemieux, Ridha Joober, et al.. (2020). Perceived utility of biological testing for autism spectrum disorder is associated with child and family functioning. Research in Developmental Disabilities. 100. 103605–103605. 8 indexed citations
15.
Deneault, Éric, Muhammad Faheem, Sean H. White, et al.. (2019). CNTN5-/+or EHMT2-/+human iPSC-derived neurons from individuals with autism develop hyperactive neuronal networks. eLife. 8. 60 indexed citations
16.
Yusuf, Afiqah, Tal Savion‐Lemieux, Ridha Joober, et al.. (2019). Association between distress and knowledge among parents of autistic children. PLoS ONE. 14(9). e0223119–e0223119. 6 indexed citations
17.
Woodbury‐Smith, Marc, Andrew D. Paterson, Mehdi Zarrei, et al.. (2018). A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees. Journal of Neurodevelopmental Disorders. 10(1). 20–20. 15 indexed citations
18.
Woodbury‐Smith, Marc, Éric Deneault, Ryan K. C. Yuen, et al.. (2017). Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly. Molecular Autism. 8(1). 59–59. 33 indexed citations
19.
Gavin, W., S. Blash, N. Hawkins, et al.. (2017). Generation of transgenic goats by pronuclear microinjection: a retrospective analysis of a commercial operation (1995–2012). Transgenic Research. 27(1). 115–122. 5 indexed citations
20.
Ding, Shou‐Wei, Jennifer Howe, Paul Keese, et al.. (1990). The tymobox, a sequence shared by most tymoviruses: its use in molecular studies of tymoviruses. Nucleic Acids Research. 18(5). 1181–1187. 77 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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