Barbara R. Pober

Also affiliated with Massachusetts General Hospital

NeuroscienceMedicineBiochemistry, 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 7 papers. Top paper: “Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams–Beuren syndrome”.

Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams–Beuren syndrome

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61522

N/A

0.561DataRank · unranked

41 citations

Zoë C. Wong, Charles J. Billington, Phoebe C. R. Parrish, Glennis Muldoon, Delong Liu +3 more

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

UNC Libraries(2020)10.17615/5188-7m66

N/A

0DataRank · unranked

0 citations

Donna M. McDonald‐McGinn, Mauricio Arcos‐Burgos, Lina M. Moreno, Andrew C. Lidral, Michel Bahuau +21 more

Williams syndrome

Nature Reviews Disease Primers(2021)10.1038/s41572-021-00276-z

N/A

0DataRank · unranked

244 citations

Boaz Barak, Chong Ae Kim, Carolyn Β. Mervis, Lucy R. Osborne, Melanie Porter +2 more

Missense variants affecting the actin-binding domains of PLS3 cause X-linked congenital diaphragmatic hernia and body wall defects

medRxiv(2021)10.1101/2021.07.07.21259278

N/A

0DataRank · unranked

2 citations

Mauro Longoni, Julie Wells, Richard S. Maser, Matthew J. Dysart, Hannah T. M. Contreras +33 more

Pathway analysis identifies novel non-synonymous variants contributing to extreme vascular outcomes in Williams-Beuren syndrome

medRxiv(2022)10.1101/2022.09.21.22280107

N/A

0DataRank · unranked

0 citations

Charles J. Billington, Niranjan Raja, Zoë C. Wong, Mark Levin, Wolfgang Resch +20 more

PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.09.002

N/A

0DataRank · unranked

8 citations

Mauro Longoni, Julie Wells, Richard S. Maser, Eric L. Bogenschutz, Matthew J. Dysart +34 more

Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams–Beuren Syndrome

Journal of the American Heart Association(2024)10.1161/jaha.123.031377

N/A

0DataRank · unranked

2 citations

Charles J. Billington, Neelam Raja, Zoë C. Wong, Mark Levin, Wolfgang Resch +20 more