Philip F. Giampietro

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 8 papers. Top paper: “Rare missense variants in FNDC1 are associated with severe adolescent idiopathic scoliosis”.

Rare missense variants in FNDC1 are associated with severe adolescent idiopathic scoliosis

Journal of Medical Genetics(2025)10.1136/jmg-2024-110586

N/A

0.104DataRank · unranked

1 citations

Gabe Haller, Julia Whittle, Momchil Nikolov, Addison Avery, José A. Morcuende +12 more

A dyadic approach to the delineation of diagnostic entities in clinical genomics

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2020.11.013

N/A

0DataRank · unranked

116 citations

Margaret P Adam, Fowzan S. Alkuraya, Anne Amemiya, Michael J. Bamshad, Anita E. Beck +42 more

TLE4 Is a Critical Mediator of Osteoblast and Runx2-Dependent Bone Development

Frontiers in Cell and Developmental Biology(2021)10.3389/fcell.2021.671029

N/A

0DataRank · unranked

6 citations

Evangelos A. Theodorou, Carl S. Holland, Rae’e Yamin, Cathleen Raggio, Philip F. Giampietro +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

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

Human Molecular Genetics(2020)10.1093/hmg/ddaa258

N/A

0DataRank · unranked

26 citations

Annabelle Enriquez, Duncan B. Sparrow, David T. Humphreys, Aideen McInerney‐Leo, Paul Leo +29 more

COL11A2 as a candidate gene for vertebral malformations and congenital scoliosis

Human Molecular Genetics(2023)10.1093/hmg/ddad117

N/A

0DataRank · unranked

22 citations

Elizabeth Wohler, Vida Erfani, Guozhuang Li, Alexya N. Aguilera, Alberto Santiago-Cornier +11 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

Myhre syndrome is caused by dominant-negative dysregulation of SMAD4 and other co-factors

Differentiation(2022)10.1016/j.diff.2022.09.002

N/A

0DataRank · unranked

18 citations

Annabelle Enriquez, Robert D. Steiner, Cathy Raggio, Megan Higgins, Di Milnes +7 more