Barbara K. Burton

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

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 13 papers. Top paper: “Newborn Screening for Mucopolysaccharidosis Type II in Illinois: An Update”.

Newborn Screening for Mucopolysaccharidosis Type II in Illinois: An Update

International Journal of Neonatal Screening(2020)10.3390/ijns6030073

N/A

1.3DataRank · unranked

25 citations

Rachel Hickey, Lauren Hitchins, Barbara K. Burton

Intrathecal idursulfase-IT in patients with neuronopathic mucopolysaccharidosis II: Results from a phase 2/3 randomized study

Molecular Genetics and Metabolism(2022)10.1016/j.ymgme.2022.07.017

N/A

0.978DataRank · unranked

49 citations

Barbara K. Burton, Paul Harmatz, Luis González Gutiérrez-Solana, Matilde Ruíz-Garcìa, Simon Jones +9 more

Long-term open-label extension study of the safety and efficacy of intrathecal idursulfase-IT in patients with neuronopathic mucopolysaccharidosis II

Molecular Genetics and Metabolism(2022)10.1016/j.ymgme.2022.07.016

N/A

0.631DataRank · unranked

26 citations

Barbara K. Burton, Paul Harmatz, Luis González Gutiérrez-Solana, Matilde Ruíz-Garcìa, Simon Jones +9 more

Newborn screening for mucopolysaccharidosis type II: Lessons learned

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.107557

N/A

0.542DataRank · unranked

14 citations

Vera Shively, Allegra Quadri, Lauren Warn, Jennifer Burton, Dorothy K. Grange +6 more

Missense variants in the voltage sensing and pore domain of KCNH5 cause neurodevelopmental phenotypes including epilepsy

medRxiv(2022)10.1101/2022.04.26.22274147

N/A

0DataRank · unranked

0 citations

Lynette G. Sadleir, Matthew Zemel, Guillem de Valles‐Ibáñez, Michael S. Hildebrand, Allyn McConkie‐Rosell +49 more

Challenges and strategies for clinical trials in propionic and methylmalonic acidemias

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.107612

N/A

0DataRank · unranked

13 citations

Barbara K. Burton, Agnieszka Jurecka, Jitendra Ganju, Beth Leiro, Roberto T. Zori +2 more

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition

Research Square(2023)10.21203/rs.3.rs-3317938/v1

N/A

0DataRank · unranked

4 citations

Ghayda Mirzaa, Keqin Yan, Raissa Relator, Sara Timpano, Binnaz Yalcin +57 more

Consensus guidelines for the monitoring and management of metachromatic leukodystrophy in the United States

Cytotherapy(2024)10.1016/j.jcyt.2024.03.487

N/A

0DataRank · unranked

25 citations

Joshua L. Bonkowsky, Jaap Jan Boelens, Eric J. Mallack, Rebecca C. Ahrens‐Nicklas, John Bernat +27 more

High precision newborn screening for mucopolysaccharidosis type I by enzymatic activity followed by endogenous, non-reducing end glycosaminoglycan analysis

Molecular Genetics and Metabolism(2024)10.1016/j.ymgme.2024.108612

N/A

0DataRank · unranked

4 citations

Francyne Kubaski, Laura Pollard, Khaja Basheeruddin, Barbara K. Burton, Joseph J. Orsini +4 more

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition

Nature Communications(2025)10.1038/s41467-025-64838-5

N/A

0DataRank · unranked

4 citations

Keqin Yan, Raissa Relator, Mathieu Lévesque, P.S. Jayasinghe, Sara Timpano +61 more

The Genetic Landscape and Epidemiology of Phenylketonuria

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.006

N/A

0DataRank · unranked

384 citations

Yair Anikster, Amaya Bélanger-Quintana, Alberto B. Burlina, Barbara K. Burton, Carla Carducci +43 more

Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5

Neurology(2022)10.1212/wnl.0000000000201492

N/A

0DataRank · unranked

24 citations

Lynette G. Sadleir, Matthew Zemel, Guillem de Valles‐Ibáñez, Michael S. Hildebrand, Allyn McConkie‐Rosell +50 more

Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling

Genetics in Medicine(2022)10.1016/j.gim.2022.07.005

N/A

0DataRank · unranked

23 citations

Rachel VanCoillie, Elizabeth VanSickle, Deanna Alexis Carere, Kara Withrow, Erin Torti +43 more