Xinying Hong

Also affiliated with University of Pennsylvania

MedicineBiochemistry, Genetics and Molecular Biology

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: “Base editing strategies for in vivo correction of two highly recurrent phenylketonuria variants”.

Base editing strategies for in vivo correction of two highly recurrent phenylketonuria variants

Molecular Therapy — Nucleic Acids(2025)10.1016/j.omtn.2025.102770

N/A

0.208DataRank · unranked

3 citations

Ishaan Jindal, Thomas R. Campion, Delaney Rutherford, Yongseok Han, Walsh Quigley +6 more

A highly multiplexed biochemical assay for analytes in dried blood spots: application to newborn screening and diagnosis of lysosomal storage disorders and other inborn errors of metabolism

Genetics in Medicine(2020)10.1038/s41436-020-0790-9

N/A

0DataRank · unranked

33 citations

Martin Sadı́lek, Michael H. Gelb, Xinying Hong

Liquid Chromatography–Tandem Mass Spectrometry in Newborn Screening Laboratories

International Journal of Neonatal Screening(2022)10.3390/ijns8040062

N/A

0DataRank · unranked

46 citations

Khaja Basheeruddin, Alberto B. Burlina, Hsiao-Jan Chen, Yin‐Hsiu Chien, George J. Dizikes +21 more

Neuron-specific ablation of the Krabbe disease gene galactosylceramidase in mice results in neurodegeneration

PLoS Biology(2022)10.1371/journal.pbio.3001661

N/A

0DataRank · unranked

15 citations

Jacob Favret, Nadav I. Weinstock, Malabika Maulik, Xinying Hong, Michael H. Gelb +4 more

Stratification of patients with lysosomal acid lipase deficiency by enzyme activity in dried blood spots

Molecular Genetics and Metabolism Reports(2022)10.1016/j.ymgmr.2022.100935

N/A

0DataRank · unranked

3 citations

Yi-Cheng Chen, Marianne Barr, Michael H. Gelb, Xinying Hong

Predicting disease severity in metachromatic leukodystrophy using protein activity and a patient phenotype matrix

Genome biology(2023)10.1186/s13059-023-03001-z

N/A

0DataRank · unranked

25 citations

Xinying Hong, Steven Froelich, Jessica Daiker, James Sacco, Hong Phuc Nguyen +7 more

Endogenous, non-reducing end glycosaminoglycan biomarkers are superior to internal disaccharide glycosaminoglycan biomarkers for newborn screening of mucopolysaccharidoses and GM1 gangliosidosis

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.107632

N/A

0DataRank · unranked

16 citations

Xinying Hong, Leslie Urdaneta, Terri Klein, Christine Waggoner, Hsuan-Chieh Liao +5 more

Newborn screening for the full set of mucopolysaccharidoses in dried blood spots based on first-tier enzymatic assay followed by second-tier analysis of glycosaminoglycans

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.107698

N/A

0DataRank · unranked

12 citations

Xinying Hong, Martin Sadı́lek, Maria Fuller, Michael H. Gelb, Zackary M. Herbst

A novel iPSC model reveals selective vulnerability of neurons in multiple sulfatase deficiency

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.108116

N/A

0DataRank · unranked

7 citations

Lívia Sertori Finoti, Margaret M. Cassidy, Jean Ann Maguire, Alyssa Gagne, Elisa A. Waxman +10 more

Multiplex tandem mass spectrometry enzymatic activity assay for the screening and diagnosis of Mucolipidosis type II and III

Molecular Genetics and Metabolism Reports(2023)10.1016/j.ymgmr.2023.100978

N/A

0DataRank · unranked

4 citations

Laura Pollard, Miao He, Michael H. Gelb, Timothy C. Wood, Xinying Hong

Combined PMM2-CDG and hereditary fructose intolerance in a patient with mild clinical presentation

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.107682

N/A

0DataRank · unranked

2 citations

Andrew C. Edmondson, Alanna Strong, Daniel Pomerantz, Emma Michl, Gerard T. Berry +2 more

Higher precision, first tier newborn screening for metachromatic leukodystrophy using 16:1-OH-sulfatide

Molecular Genetics and Metabolism(2024)10.1016/j.ymgme.2024.108436

N/A

0DataRank · unranked

9 citations

Annette Bley, Heather A. Brown, Charlotte Chanson, Heather J. Church, Michael H. Gelb +10 more

Hematopoietic stem cell gene therapy improves outcomes in a clinically relevant mouse model of multiple sulfatase deficiency

Molecular Therapy(2024)10.1016/j.ymthe.2024.08.015

N/A

0DataRank · unranked

3 citations

Lucas Tricoli, Xinying Hong, Parith Wongkittichote, Carlo Castruccio Castracani, Amaliris Guerra +11 more

Hematopoietic stem cell gene therapy improves outcomes in a clinically relevant mouse model of Multiple Sulfatase Deficiency

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.03.08.584099

N/A

0DataRank · unranked

0 citations

Lucas Tricoli, Xinying Hong, Parith Wongkittichote, Carlo Castruccio Castracani, Amaliris Guerra +11 more

Toward newborn screening of metachromatic leukodystrophy: results from analysis of over 27,000 newborn dried blood spots

Genetics in Medicine(2020)10.1038/s41436-020-01017-5

N/A

0DataRank · unranked

69 citations

Jessica Daiker, Martin Sadı́lek, Nicole Ruiz-Schultz, Arun Kumar, Stevie Norcross +7 more

Newborn screening for metachromatic leukodystrophy: Preparation of reagents and methodology for measurement of sulfatides and arylsulfatase A enzymatic activity in dried blood spots

Molecular Genetics and Metabolism(2025)10.1016/j.ymgme.2025.109138

N/A

0DataRank · unranked

2 citations

Khaja Basheeruddin, Soumeya Bekri, Heather A. Brown, Heather J. Church, Justin Gianares +11 more