Dusica Babovic‐Vuksanovic

Also affiliated with Mayo Clinic in Florida

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 8 papers. Top paper: “Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation”.

Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation

Genetics in Medicine(2022)10.1016/j.gim.2022.05.007

N/A

0.846DataRank · unranked

281 citations

Ludwine Messiaen, Eric Legius, Patrice Pancza, Robert A. Avery, Jaishri O. Blakeley +79 more

Audit of Gastrointestinal Manifestations in Patients with Loeys–Dietz Syndrome and Vascular Ehlers–Danlos Syndrome

Digestive Diseases and Sciences(2020)10.1007/s10620-020-06265-8

N/A

0.396DataRank · unranked

13 citations

Mary Babameto, Dusica Babovic‐Vuksanovic, Juan M. Bowen, Michael Camilleri, Xiao‐Jing Wang

TSPEAR variants are primarily associated with ectodermal dysplasia and tooth agenesis but not hearing loss: A novel cohort study

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62347

N/A

0DataRank · unranked

20 citations

Alejandro Ferrer, Carla Nishimura, Filippo Pinto e Vairo, Tristan Rey, Bruno Leheup +27 more

Pathogenic mutations in the chromokinesin KIF22 disrupt anaphase chromosome segregation

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.09.29.462402

N/A

0DataRank · unranked

1 citations

Patrick R. Blackburn, Noah S Arons, Sarah N Stevens, Dusica Babovic‐Vuksanovic, Jane B. Lian +3 more

Pathogenic mutations in the chromokinesin KIF22 disrupt anaphase chromosome segregation

eLife(2022)10.7554/elife.78653

N/A

0DataRank · unranked

23 citations

Patrick R. Blackburn, Noah S Arons, Sarah N Stevens, Dusica Babovic‐Vuksanovic, Jane B. Lian +3 more

Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development

Neuron(2020)10.1016/j.neuron.2020.01.042

N/A

0DataRank · unranked

223 citations

Mariah L. Hoye, Ruiji Jiang, Bethany Johnson-Kerner, Lindsey Suit, Srivats Venkataramanan +49 more

Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypes

iScience(2023)10.1016/j.isci.2023.106818

N/A

0DataRank · unranked

33 citations

Kristian Assing, Safa Barış, Stephanie L. Safgren, Işık Somuncu Johansen, Marianne Antonius Jakobsen +20 more

SPECC1L regulates palate development downstream of IRF6

Human Molecular Genetics(2020)10.1093/hmg/ddaa002

N/A

0DataRank · unranked

27 citations

Luke W. Wenger, Nathan R. Wilson, Sraavya S Undurty-Akella, Jennifer Standley, Eno-Abasi Augustine-Akpan +23 more