Lina Ghaloul‐Gonzalez

Biochemistry, 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 10 papers. Top paper: “A porcine model of phenylketonuria generated by CRISPR/Cas9 genome editing”.

A porcine model of phenylketonuria generated by CRISPR/Cas9 genome editing

JCI Insight(2020)10.1172/jci.insight.141523

N/A

0DataRank · unranked

45 citations

Bethany K. Redel, Marie A. Johnson, Kristen J. Skvorak, Lina Ghaloul‐Gonzalez, Megan E. Yates +21 more

Development and characterization of a mouse model for Acad9 deficiency

Molecular Genetics and Metabolism(2021)10.1016/j.ymgme.2021.09.002

N/A

0DataRank · unranked

12 citations

Al‐Walid Mohsen, Kailyn Bloom, Anuradha Karunanidhi, Sivakama S. Bharathi, Yijen Wu +6 more

Natural history of TANGO2 deficiency disorder: Baseline assessment of 73 patients

Genetics in Medicine(2022)10.1016/j.gim.2022.11.020

N/A

0DataRank · unranked

50 citations

Erica Julianne Lay, Claudia Soler‐Alfonso, Kevin E. Glinton, Kimberly Houck, Mustafa Tosur +29 more

Mitochondrial dysfunction associated with TANGO2 deficiency

Scientific Reports(2022)10.1038/s41598-022-07076-9

N/A

0DataRank · unranked

48 citations

Al‐Walid Mohsen, Anuradha Karunanidhi, Claudette M. St. Croix, Simon C. Watkins, Erik Koppes +4 more

Prevalence of Pathogenic and Potentially Pathogenic Inborn Error of Immunity Associated Variants in Children with Severe Sepsis

Journal of Clinical Immunology(2022)10.1007/s10875-021-01183-4

N/A

0DataRank · unranked

24 citations

Lina Ghaloul‐Gonzalez, Jerry Vockley, Janette Lamb, Deborah Hollingshead, Uma Chandran +21 more

Natural history of propionic acidemia in the Amish population

Molecular Genetics and Metabolism Reports(2022)10.1016/j.ymgmr.2022.100936

N/A

0DataRank · unranked

12 citations

Catherine Walsh Vockley, Paige Heiman, Zineb Ammous, Olivia Wenger, Jerry Vockley +2 more

ITCH deficiency clinical phenotype expansion and mitochondrial dysfunction

Molecular Genetics and Metabolism Reports(2022)10.1016/j.ymgmr.2022.100932

N/A

0DataRank · unranked

5 citations

Paige Heiman, Olivia D’Annibale, Anuradha Karunanidhi, Alyssa Powers, Marianne McGuire +8 more

Identification of Two Homozygous Variants in MYBPC3 and SMYD1 Genes Associated with Severe Infantile Cardiomyopathy

Genes(2023)10.3390/genes14030659

N/A

0DataRank · unranked

3 citations

Miguel Reyes‐Múgica, Daniel F. Marker, Ana M. Gómez, Matthew Zinn, Leslie Walsh +4 more

De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.02.007

N/A

0DataRank · unranked

10 citations

Alice M. Tao, Shenzhao Lu, Mengqi Ma, Shabab B. Hannan, Rachel Slaugh +43 more

The Crystal Structure of Human Transport and Golgi Organization 2 Homolog ( TANGO2 ) Protein Reveals an αββα‐Fold Arrangement

Proteins Structure Function and Bioinformatics(2025)10.1002/prot.70023

N/A

0DataRank · unranked

2 citations

Alyssa Powers, K.P. Battaile, Al‐Walid Mohsen, David K. Johnson, Scott Lovell +2 more