🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Katherine A. Rauen

California State University, Sacramento

ORCID: 0000-0003-1719-7228

Also affiliated with University of California, Davis

Biochemistry, Genetics and Molecular BiologyMedicineImmunology and Microbiology

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

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 15 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

Advancing RAS/RASopathy therapies: An NCI‐sponsored intramural and extramural collaboration for the study of RASopathies

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61485

N/A

0.624DataRank · unranked

63 citations

Megan N. Frone, Karen W. Gripp, Bruce D. Gelb, Lisa Schoyer, Lisa Schill +17 more

A novel DPH5-related diphthamide-deficiency syndrome causing embryonic lethality or profound neurodevelopmental disorder

Genetics in Medicine(2022)10.1016/j.gim.2022.03.014

N/A

0.425DataRank · unranked

16 citations

Kristin Grimsrud, Louise Lanoue, Alena Egense, Brandon Willis, Johanna Hörberg +95 more

Ophthalmic manifestations in Costello syndrome caused by Ras pathway dysregulation during development

Ophthalmic Genetics(2021)10.1080/13816810.2021.1978103

N/A

0.385DataRank · unranked

12 citations

Reshmitha Fallurin, Tonya Watson, Prabhu Shankar, Terri L. Young, Deborah Orel‐Bixler +2 more

Translating multiscale research in rare disease

Disease Models & Mechanisms(2024)10.1242/dmm.052009

N/A

0.104DataRank · unranked

1 citations

Monica J. Justice, Monkol Lek, Karen Liu, Katherine A. Rauen, Kirsty M. Hooper

Cross-species analysis of LZTR1 loss-of-function mutants demonstrates dependency to RIT1 orthologs

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.01.04.474894

N/A

0.104DataRank · unranked

1 citations

Laura Rodríguez-Muñoz, Joaquím Grego‐Bessa, Alice Cheng, Katherine A. Rauen, Anatoly Urisman +4 more

MEK-inhibitor-mediated rescue of skeletal myopathy caused by activating Hras mutation in a Costello syndrome mouse model

Disease Models & Mechanisms(2021)10.1242/dmm.049166

N/A

0DataRank · unranked

26 citations

Alice F. Goodwin, Yoshiko Maeda, Ophir D. Klein, Katherine A. Rauen, William E. Tidyman

Obstetrical and neonatal outcomes of cardio‐facio‐cutaneous syndrome: Prenatal consequences of Ras/MAPK dysregulation

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.63020

N/A

0DataRank · unranked

5 citations

Amanda Mahle, Susan H Tran, Teresa N. Sparks, Katherine A. Rauen, Angie C. Jelin

A novel DPH5-related diphthamide-deficiency syndrome causing embryonic lethality or profound neurodevelopmental disorder

Genetics in Medicine(2022)10.1016/j.gim.2022.07.021

N/A

0DataRank · unranked

4 citations

Kristin Grimsrud, Louise Lanoue, Alena Egense, Brandon Willis, Johanna Hörberg +15 more

RAS pathway influences the number of melanocytic nevi in cardiofaciocutaneous and Costello syndromes

Journal of the American Academy of Dermatology(2020)10.1016/j.jaad.2020.01.038

N/A

0DataRank · unranked

12 citations

J. Urban, Guannan Zhu, Iryna Rybak, Jessica R. Terrell, Lihong Qi +4 more

Melanocytic neoplasms in neurofibromatosis type 1: a systematic review

Melanoma Research(2023)10.1097/cmr.0000000000000912

N/A

0DataRank · unranked

8 citations

Elanee Simmons, Amy Studer, Katherine A. Rauen, Maija Kiurua, Summer N. Meyer

The 8th International RASopathies Symposium: Expanding research and care practice through global collaboration and advocacy

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63477

N/A

0DataRank · unranked

7 citations

Anton M. Bennett, Lisa Schoyer, Beth Stronach, April Anschutz, Sarah C. Borrie +39 more

RASopathies – what they reveal about RAS/MAPK signaling in skeletal muscle development

Disease Models & Mechanisms(2024)10.1242/dmm.050609

N/A

0DataRank · unranked

12 citations

William E. Tidyman, Katherine A. Rauen

Recurrent p.H119Y variant in MAP2K1 expands the phenotypic spectrum of MAP2K1‐related RASopathy

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63854

N/A

0DataRank · unranked

0 citations

Daniel Wegner, Jennifer Wambach, Kathleen Sisco, Stephen Stone, Jonathan H. Sheehan +6 more

The seventh international RASopathies symposium: Pathways to a cure—expanding knowledge, enhancing research, and therapeutic discovery

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62716

N/A

0DataRank · unranked

16 citations

Amy E. Roberts, Lisa Schill, Lisa Schoyer, Beth Stronach, Grégor Andelfinger +37 more