Scott M. Paul

National Institutes of Health Clinical Center

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 9 papers. Top paper: “Selumetinib in Children with Inoperable Plexiform Neurofibromas”.

Selumetinib in Children with Inoperable Plexiform Neurofibromas

New England Journal of Medicine(2020)10.1056/nejmoa1912735

N/A

9.0DataRank · unranked

708 citations

Pamela L. Wolters, Eva Dombi, Andrea Baldwin, Patricia Whitcomb, Michael J. Fisher +24 more

Safety and Efficacy of Denosumab for Fibrous Dysplasia of Bone

New England Journal of Medicine(2023)10.1056/nejmc2214862

N/A

1.8DataRank · unranked

67 citations

Zachary Michel, Kristen S. Pan, Jocelyn Taylor, Vivian Szymczuk, Sriram S. Paravastu +9 more

Selumetinib in children with neurofibromatosis type 1 and asymptomatic inoperable plexiform neurofibroma at risk for developing tumor-related morbidity

Neuro-Oncology(2022)10.1093/neuonc/noac109

N/A

1.7DataRank · unranked

66 citations

Brittany Glassberg, Pamela L. Wolters, Eva Dombi, Andrea Baldwin, Michael J. Fisher +18 more

TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy

Human Genetics(2021)10.1007/s00439-021-02379-9

N/A

0.510DataRank · unranked

29 citations

Brenda J. Barry, Caroline D. Robson, Flavia M. Facio, Carol Van Ryzin, Wai‐Man Chan +31 more

Updated consensus guidelines on the management of Phelan–McDermid syndrome

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63312

N/A

0DataRank · unranked

49 citations

Mustafa Sahin, Joseph D. Buxbaum, Elizabeth Berry‐Kravis, Latha Soorya, Audrey Thurm +40 more

Systematic phenotype and genotype characterization of Moebius syndrome

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103437

N/A

0DataRank · unranked

1 citations

Julie A. Jurgens, Narisu Narisu, Zhongyang Zhang, Brenda J. Barry, Carol Van Ryzin +37 more

Neonatal-Onset Multisystem Inflammatory Disease Responsive to Interleukin-1β Inhibition

UNC Libraries(2020)10.17615/z694-np66

N/A

0DataRank · unranked

0 citations

Bracha Shaham, Scott Penzak, Frank Pucino, Kathleen M. O’Neil, Robert C. Fuhlbrigge +27 more

Debilitating hip degeneration in trichothiodystrophy: Association with ERCC2/XPD mutations, osteosclerosis, osteopenia, coxa valga, contractures, and osteonecrosis

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62962

N/A

0DataRank · unranked

9 citations

Grant Randall, Alexandra Edelman, Rina Allawh, Michael Xiong, Deborah Tamura +7 more

RANKL inhibition with denosumab improves fibrous dysplasia by decreasing lesional cell proliferation and increasing osteogenesis

medRxiv(2022)10.1101/2022.10.24.22281375

N/A

0DataRank · unranked

4 citations

Jarred M. Whitlock, Zachary Michel, Kristen S. Pan, Jocelyn Taylor, Vivian Szymczuk +12 more