Jennifer A. Sullivan

5.3k total citations
51 papers, 1.7k citations indexed

About

Jennifer A. Sullivan is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Jennifer A. Sullivan has authored 51 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 12 papers in Molecular Biology and 8 papers in Physiology. Recurrent topics in Jennifer A. Sullivan's work include Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (9 papers) and Autism Spectrum Disorder Research (7 papers). Jennifer A. Sullivan is often cited by papers focused on Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (9 papers) and Autism Spectrum Disorder Research (7 papers). Jennifer A. Sullivan collaborates with scholars based in United States, Australia and France. Jennifer A. Sullivan's co-authors include Priya S. Kishnani, Allyn McConkie‐Rosell, Gail A. Spiridigliozzi, Albert S.B. Edge, Daniela Sachs, Laura P. Svetkey, Susanne B. Haga, Rachel Mills, Huntington F. Willard and Geoffrey S. Ginsburg and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Immunology and Human Molecular Genetics.

In The Last Decade

Jennifer A. Sullivan

50 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jennifer A. Sullivan United States	23	769	463	416	364	213	51	1.7k
Juan Clinton Llerena Brazil	23	601 0.8×	291 0.6×	400 1.0×	219 0.6×	143 0.7×	112	1.6k
Nancy J. Mendelsohn United States	26	859 1.1×	650 1.4×	651 1.6×	422 1.2×	391 1.8×	51	2.1k
Hüseyin Önay Türkiye	24	441 0.6×	177 0.4×	754 1.8×	107 0.3×	223 1.0×	205	2.0k
Richard W. Erbe United States	25	549 0.7×	293 0.6×	973 2.3×	422 1.2×	96 0.5×	65	2.4k
Pranesh Chakraborty Canada	27	474 0.6×	185 0.4×	802 1.9×	108 0.3×	197 0.9×	100	2.0k
Nanbert Zhong United States	25	210 0.3×	359 0.8×	630 1.5×	85 0.2×	357 1.7×	87	1.8k
Nobutake Matsuo Japan	32	1.2k 1.6×	205 0.4×	1.5k 3.6×	191 0.5×	105 0.5×	107	3.2k
Emmanouil Rampakakis Canada	24	291 0.4×	104 0.2×	526 1.3×	375 1.0×	429 2.0×	150	2.3k
Gail E. Graham Canada	23	549 0.7×	95 0.2×	786 1.9×	77 0.2×	261 1.2×	60	1.9k
Justine A. Ellis Australia	31	485 0.6×	338 0.7×	598 1.4×	140 0.4×	174 0.8×	93	2.6k

Countries citing papers authored by Jennifer A. Sullivan

Since Specialization

Citations

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

Fields of papers citing papers by Jennifer A. Sullivan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jennifer A. Sullivan

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Sullivan, Jennifer A., et al.. (2024). The book is just being written: The enduring journey of parents of children with emerging‐ ultrarare disorders. Journal of Genetic Counseling. 34(1). e1894–e1894. 2 indexed citations

Sandal, Priyanka, Chian Ju Jong, Ronald A. Merrill, et al.. (2024). De novo missense variants in the PP2A regulatory subunit PPP2R2B in a neurodevelopmental syndrome: potential links to mitochondrial dynamics and spinocerebellar ataxias. Human Molecular Genetics. 34(2). 193–203. 1 indexed citations

Sullivan, Jennifer A., Rebecca C. Spillmann, Kelly Schoch, et al.. (2023). The best of both worlds: Blending cutting‐edge research with clinical processes for a productive exome clinic. Clinical Genetics. 105(1). 62–71.

McConkie‐Rosell, Allyn, Rebecca C. Spillmann, Kelly Schoch, et al.. (2023). Unraveling non‐participation in genomic research: A complex interplay of barriers, facilitators, and sociocultural factors. Journal of Genetic Counseling. 32(5). 993–1008. 7 indexed citations

Sullivan, Jennifer A., et al.. (2021). VA Compassionate Contact Corps: A Phone-Based Intervention for Veterans Interested In Speaking With Peers. Innovation in Aging. 5(Supplement_1). 204–204. 5 indexed citations

Stanek, Lisa M., Kousaku Ohno, Lluı́s Samaranch, et al.. (2018). Extensive Transduction and Enhanced Spread of a Modified AAV2 Capsid in the Non-human Primate CNS. Molecular Therapy. 26(10). 2418–2430. 46 indexed citations

Sullivan, Jennifer A., Lisa M. Stanek, Michael Lukason, et al.. (2018). Rationally designed AAV2 and AAVrh8R capsids provide improved transduction in the retina and brain. Gene Therapy. 25(3). 205–219. 27 indexed citations

McNamara, Erin R., Jennifer A. Sullivan, Shashi Nagaraj, John S. Wiener, & Priya S. Kishnani. (2014). Neurogenic Bladder Dysfunction Presenting as Urinary Retention in Neuronopathic Gaucher Disease. JIMD Reports. 15. 67–70. 3 indexed citations

Passini, Marco A., Jie Bu, Amy M. Richards, et al.. (2014). Translational Fidelity of Intrathecal Delivery of Self-Complementary AAV9–Survival Motor Neuron 1 for Spinal Muscular Atrophy. Human Gene Therapy. 25(7). 619–630. 72 indexed citations

10.

Haga, Susanne B., William T. Barry, Rachel Mills, et al.. (2013). Public Knowledge of and Attitudes Toward Genetics and Genetic Testing. Genetic Testing and Molecular Biomarkers. 17(4). 327–335. 190 indexed citations

11.

Yepes, Juan F., et al.. (2007). Hypercoagulability syndromes: what the dentist needs to know. Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology. 104(1). 3–11. 3 indexed citations

12.

Heller, James H., Gail A. Spiridigliozzi, Blythe G. Crissman, et al.. (2006). Safety and Efficacy of Rivastigmine in Adolescents with Down Syndrome: A Preliminary 20-Week, Open-Label Study. Journal of Child and Adolescent Psychopharmacology. 16(6). 755–765. 33 indexed citations

13.

Basinger, Alice, Jessica K. Booker, Dianne M. Frazier, et al.. (2006). Glutaric acidemia type 1 in patients of Lumbee heritage from North Carolina. Molecular Genetics and Metabolism. 88(1). 90–92. 23 indexed citations

14.

Hanna, R M, Marie McDonald, Jennifer A. Sullivan, et al.. (2004). Diagnostic and treatment challenges of neuronopathic Gaucher disease: Two caseswith an intermediate phenotype. Journal of Inherited Metabolic Disease. 27(5). 687–690. 1 indexed citations

15.

Heller, James H., Gail A. Spiridigliozzi, Jennifer A. Sullivan, et al.. (2002). Donepezil for the treatment of language deficits in adults with Down syndrome: A preliminary 24‐week open trial. American Journal of Medical Genetics Part A. 116A(2). 111–116. 44 indexed citations

16.

Chen, Yuan‐Tsong, Deeksha Bali, & Jennifer A. Sullivan. (2002). Prenatal diagnosis in glycogen storage diseases. Prenatal Diagnosis. 22(5). 357–359. 5 indexed citations

17.

McConkie‐Rosell, Allyn, Gail A. Spiridigliozzi, Jennifer A. Sullivan, Deborah V. Dawson, & Ave M. Lachiewicz. (2001). Longitudinal study of the carrier testing process for fragile X syndrome: Perceptions and coping. American Journal of Medical Genetics. 98(1). 37–45. 1 indexed citations

18.

Amalfitano, Andrea, A. Resai Bengur, Richard P. Morse, et al.. (2001). Recombinant human acid α-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial. Genetics in Medicine. 3(2). 132–138. 293 indexed citations

19.

Scaria, Abraham, Jennifer A. Sullivan, Judith A. St. George, et al.. (2000). Adenoviral Vector Expressing ICP47 Inhibits Adenovirus-Specific Cytotoxic T Lymphocytes in Nonhuman Primates. Molecular Therapy. 2(5). 505–514. 10 indexed citations

20.

McConkie‐Rosell, Allyn, Gail A. Spiridigliozzi, Jennifer A. Sullivan, Deborah V. Dawson, & Ave M. Lachiewicz. (2000). Longitudinal study of the carrier testing process for fragile X syndrome: Perceptions and coping. American Journal of Medical Genetics. 98(1). 37–45. 29 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.

Explore authors with similar magnitude of impact