Laura Schultz‐Rogers

University of North Carolina at Chapel Hill

Also affiliated with Mayo Clinic, Emma Kinderziekenhuis, Mayo Clinic in Florida, Amsterdam University Medical Centers, University of Colorado Anschutz Medical Campus, University of Amsterdam

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 8 papers. Top paper: “Haploinsufficiency as a disease mechanism in GNB1‐associated neurodevelopmental disorder”.

Haploinsufficiency as a disease mechanism in GNB1‐associated neurodevelopmental disorder

Molecular Genetics & Genomic Medicine(2020)10.1002/mgg3.1477

N/A

0DataRank · unranked

18 citations

Ikuo Masuho, Filippo Pinto e Vairo, Christopher T. Schmitz, Tanya L. Schwab, Karl J. Clark +6 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

A homozygous missense variant in UBE2T is associated with a mild Fanconi anemia phenotype

Haematologica(2020)10.3324/haematol.2020.259275

N/A

0DataRank · unranked

5 citations

Francis P. Lach, Kimberly A. Rickman, Alejandro Ferrer, Abhishek A. Mangaonkar, Tanya L. Schwab +10 more

Pathogenic SPTBN1 variants cause a novel autosomal dominant neurodevelopmental syndrome

medRxiv(2020)10.1101/2020.08.31.20184481

N/A

0DataRank · unranked

3 citations

Keith A. Breau, Blake A. Creighton, Rebecca C. Spillmann, Erin Torti, Sruthi Dontu +63 more

Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome

Nature Genetics(2021)10.1038/s41588-021-00886-z

N/A

0DataRank · unranked

108 citations

Blake A. Creighton, Keith A. Breau, Rebecca C. Spillmann, Erin Torti, Sruthi Dontu +70 more

SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.01.015

N/A

0DataRank · unranked

93 citations

Kaifang Pang, Andrea Ciolfi, Michael A. Levy, Andrés Hernández, Lucia Pedace +95 more

Rbbp4 loss disrupts neural progenitor cell cycle regulation independent of Rb and leads to Tp53 acetylation and apoptosis

Developmental Dynamics(2022)10.1002/dvdy.467

N/A

0DataRank · unranked

17 citations

Michelle L. Thayer, Sekhar Kambakam, Wesley A. Wierson, Jordan A. Helmer, Mark Wishman +12 more

Bi-allelic variants in INTS11 are associated with a complex neurological disorder

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.03.012

N/A

0DataRank · unranked

38 citations

Erica L. Macke, Marcello Niceta, Monika Weisz Hubshman, Oguz Kanca, Laura Schultz‐Rogers +95 more