Eric A. Pierce

Also affiliated with Massachusetts Eye and Ear Infirmary, Harvard University

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 16 papers. Top paper: “Gene Editing for CEP290 -Associated Retinal Degeneration”.

Gene Editing for CEP290 -Associated Retinal Degeneration

New England Journal of Medicine(2024)10.1056/nejmoa2309915

N/A

3.3DataRank · unranked

204 citations

Tomás S. Alemán, Kanishka T. Jayasundera, Bright S. Ashimatey, Keunpyo Kim, Alia Rashid +9 more

Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.03.008

N/A

0.489DataRank · unranked

25 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 more

Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases

medRxiv(2024)10.1101/2024.12.22.24319370

N/A

0.104DataRank · unranked

1 citations

Kristen M. Laricchia, Nicole J. Lake, Sushma Chaluvadi, Vijay Ganesh, Stephanie DiTroia +30 more

Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis

medRxiv(2023)10.1101/2023.08.08.23293829

N/A

0DataRank · unranked

8 citations

Gabrielle Lemire, Maha S. Zaki, Mariel Wissman, Wathone Win, S. White +70 more

Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease

medRxiv(2023)10.1101/2023.10.05.23296595

N/A

0DataRank · unranked

1 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 more

Genome Sequencing for Diagnosing Rare Diseases

New England Journal of Medicine(2024)10.1056/nejmoa2314761

N/A

0DataRank · unranked

189 citations

Gabrielle Lemire, Eva Berger, Maha S. Zaki, Mariel Wissmann, Wathone Win +84 more

Substitution of a single non-coding nucleotide upstream of TMEM216 causes non-syndromic retinitis pigmentosa and is associated with reduced TMEM216 expression

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.020

N/A

0DataRank · unranked

7 citations

Pooja Biswas, Anne-Marie Berry, Riccardo Sangermano, Mukhtar Ullah, Siying Lin +40 more

Optimized Prime Editing of Human Induced Pluripotent Stem Cells to Efficiently Generate Isogenic Models of Mendelian Diseases

International Journal of Molecular Sciences(2024)10.3390/ijms26010114

N/A

0DataRank · unranked

5 citations

Alba Ortega-Gascó, Hafiz Muhammad Azhar Baig, Nathan Ehrenreich, Thibaud Metais, Michael J. Scandura +4 more

Systematic empirical evaluation of individual base editing targets: validating therapeutic targets in USH2A and comparison of methods

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.10.02.615422

N/A

0DataRank · unranked

0 citations

Kannan Vrindavan Manian, Rossano Butcher, Jonathan M. Levy, Nachiket Pendse, Erin Hennessey +5 more

Systematic empirical evaluation of individual base editing targets: Validating therapeutic targets in USH2A and comparison of methods

Molecular Therapy(2025)10.1016/j.ymthe.2025.01.042

N/A

0DataRank · unranked

11 citations

Kannan Vrindavan Manian, Rossano Butcher, Jonathan M. Levy, Nachiket Pendse, Erin Hennessey +5 more

Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy

Genetics in Medicine(2025)10.1016/j.gim.2025.101401

N/A

0DataRank · unranked

4 citations

Maayan Avraham, Sandeep Sarma Asodu, Abigail R. Moye, Riccardo Sangermano, Leah Rizel +19 more

Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100441

N/A

0DataRank · unranked

1 citations

Kristen M. Laricchia, Nicole J. Lake, Sushma Chaluvadi, Vijay Ganesh, Stephanie DiTroia +31 more

Investigating cone photoreceptor development using patient-derived NRL null retinal organoids

Communications Biology(2020)10.1038/s42003-020-0808-5

N/A

0DataRank · unranked

102 citations

Elizabeth E. Capowski, Jie Wang, Aniruddha M. Kaushik, Alex D. Jansen, Kimberly L. Edwards +9 more

Identifying genetic determinants of outer retinal function in mice using a large-scale gene-targeted screen

PLoS Genetics(2025)10.1371/journal.pgen.1011886

N/A

0DataRank · unranked

0 citations

Mark P. Krebs, Riccardo Sangermano, Jessica K. Wong, Cynthia L. Smith, Amelia Willett +14 more

Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.04.005

N/A

0DataRank · unranked

55 citations

Xénia Latypova, Lokuliyanage Dona Samudita Senaratne, Ludovic Martin, Daniel C. Koboldt, Georgios Kellaris +72 more

Generation of a human induced pluripotent stem cell line (OGIi001) from peripheral blood mononuclear cells of a healthy male donor

Stem Cell Research(2023)10.1016/j.scr.2023.103280

N/A

0DataRank · unranked

2 citations

Laurence Dahéron, Rodrigo Cerna-Chavez, Emily Place, Rachel M. Huckfeldt, Eric A. Pierce +2 more