Sarah Silverstein

Rutgers, The State University of New Jersey

Also affiliated with National Institutes of Health, National Institute of Neurological Disorders and Stroke, Institute of Social Work, Rutgers New Jersey Medical School

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 9 papers. Top paper: “CIAO1 loss of function causes a neuromuscular disorder with compromise of nucleocytoplasmic Fe-S enzymes”.

CIAO1 loss of function causes a neuromuscular disorder with compromise of nucleocytoplasmic Fe-S enzymes

Journal of Clinical Investigation(2024)10.1172/jci179559

N/A

0.449DataRank · unranked

19 citations

Rotem Orbach, Irina Zaharieva, Ana Töpf, Sandra Donkervoort, Pinki Munot +20 more

A humanized knock-in Col6a1 mouse recapitulates a deep-intronic splice-activating variant

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.03.21.581572

N/A

0.104DataRank · unranked

1 citations

Fady Guirguis, Berit Lubben, Lindsey Trank, Sarah Silverstein, Astrid Brull +5 more

Clinical, immunohistochemical, and genetic characterization of splice-altering biallelic DES variants: Therapeutic implications

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100274

N/A

0DataRank · unranked

2 citations

Chamindra G. Laverty, Sandra Donkervoort, Ying Hu, Sarah Silverstein, Sarah Neuhaus +12 more

Differential inclusion of NEB exons 143 and 144 provides insight into NEB -related myopathy variant interpretation and disease manifestation

medRxiv(2024)10.1101/2024.03.25.24304535

N/A

0DataRank · unranked

0 citations

Rotem Orbach, Safoora Syeda, A. Reghan Foley, Svetlana Gorokhova, Katherine G. Meilleur +6 more

Differential inclusion of NEB exons 143 and 144 provides insight into NEB-related myopathy variant interpretation and disease manifestation

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100354

N/A

0DataRank · unranked

0 citations

Rotem Orbach, Safoora Syeda, A. Reghan Foley, Svetlana Gorokhova, Katherine G. Meilleur +6 more

Collagen type VI regulates TGF-β bioavailability in skeletal muscle in mice

Journal of Clinical Investigation(2025)10.1172/jci173354

N/A

0DataRank · unranked

14 citations

Hailey Hearn, Jachinta E. Rooney, Yaqun Zou, Kory R. Johnson, Gina Norato +9 more

RNA sequencing driven diagnosis expands the phenotypic spectrum of NBAS deficiency

Molecular Genetics and Metabolism(2025)10.1016/j.ymgme.2025.109105

N/A

0DataRank · unranked

3 citations

Thomas Cassini, Jiayu Fu, Barbara N. Pusey, Ellen F. Macnamara, F. Graeme Frost +7 more

BCS1L‐Associated Disease: 5′‐UTR Variant Shifts the Phenotype Towards Axonal Neuropathy

Annals of Clinical and Translational Neurology(2025)10.1002/acn3.70108

N/A

0DataRank · unranked

0 citations

Nunziata Maio, Russell J. Butterfield, A. Reghan Foley, Sarah Silverstein, Yan Li +7 more

Mitochondrial trifunctional protein deficiency caused by a deep intronic deletion leading to aberrant splicing

JIMD Reports(2024)10.1002/jmd2.12459

N/A

0DataRank · unranked

4 citations

Sarah Silverstein, Molly Behan, Cynthia J. Tifft, May Christine V. Malicdan, David R. Adams +4 more