Jessica Alföldi

Broad Institute — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

42h-index26.3kcitations103works40.02yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Genomics and Phylogenetic Studies(25), Genomics and Rare Diseases(22), Virus-based gene therapy research(17), Cancer Genomics and Diagnostics(16), Sarcoma Diagnosis and Treatment(14)

Publications98 total

Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database
Nature Communications·2025· 3 citedOpen Access
The effect of LRRK2 loss-of-function variants in humans
UNC Libraries·2025Open Access
Author Correction: The effect of LRRK2 loss-of-function variants in humans
UNC Libraries·2025Open Access
Author Correction: A genomic mutational constraint map using variation in 76,156 human genomes
Nature·2024· 157 citedOpen Access
A genomic mutational constraint map using variation in 76,156 human genomes
Nature·2023· 1.1k citedOpen Access
Inferring compound heterozygosity from large-scale exome sequencing data
Nature Genetics·2023· 30 citedOpen Access
Data from Comparative Genomics Reveals Shared Mutational Landscape in Canine Hemangiosarcoma and Human Angiosarcoma
2023Open Access
Supplemental Table 7 from Comparative Genomics Reveals Shared Mutational Landscape in Canine Hemangiosarcoma and Human Angiosarcoma
2023Open Access
Supplemental Table 7 from Comparative Genomics Reveals Shared Mutational Landscape in Canine Hemangiosarcoma and Human Angiosarcoma
2023Open Access
Supplementary Methods from Comparative Genomics Reveals Shared Mutational Landscape in Canine Hemangiosarcoma and Human Angiosarcoma
2023Open Access
Supplementary Tables and Figures from Comparative Genomics Reveals Shared Mutational Landscape in Canine Hemangiosarcoma and Human Angiosarcoma
2023Open Access
Data from Comparative Genomics Reveals Shared Mutational Landscape in Canine Hemangiosarcoma and Human Angiosarcoma
2023Open Access
Supplementary Tables and Figures from Comparative Genomics Reveals Shared Mutational Landscape in Canine Hemangiosarcoma and Human Angiosarcoma
2023Open Access
Supplementary Methods from Comparative Genomics Reveals Shared Mutational Landscape in Canine Hemangiosarcoma and Human Angiosarcoma
2023Open Access
Supplementary Table 5 from <i>SETD2</i> Is Recurrently Mutated in Whole-Exome Sequenced Canine Osteosarcoma
2023Open Access
Supplementary Table 14 from <i>SETD2</i> Is Recurrently Mutated in Whole-Exome Sequenced Canine Osteosarcoma
2023Open Access
Supplementary Tables 1-14 from <i>SETD2</i> Is Recurrently Mutated in Whole-Exome Sequenced Canine Osteosarcoma
2023Open Access
Supplementary Figures 1-8 from <i>SETD2</i> Is Recurrently Mutated in Whole-Exome Sequenced Canine Osteosarcoma
2023Open Access
Supplementary Table 5 from <i>SETD2</i> Is Recurrently Mutated in Whole-Exome Sequenced Canine Osteosarcoma
2023Open Access
Data from <i>SETD2</i> Is Recurrently Mutated in Whole-Exome Sequenced Canine Osteosarcoma
2023Open Access
page 1 of 5Next →

Frequent Co-authors

Kerstin Lindblad‐Toh(23), Konrad J. Karczewski(19), Laurent C. Francioli(17), Beryl B. Cummings(17), Jeremy Johnson(17), Nicholas A. Watts(16), Laura D. Gauthier(15), Federica Di Palma(15), Ryan L. Collins(14), Matthew Solomonson(14), Eric Banks(14), Anne O’Donnell‐Luria(14), Namrata Gupta(14), Mark J. Daly(14), Qingbo S. Wang(13), Timothy Poterba(13), Irina M. Armean(13), Louis Bergelson(13), Stacey Gabriel(13), Ruchi Munshi(13)