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

Christina G.S. Palmer

University of Colorado Hospital

ORCID: 0009-0005-6253-8425

Also affiliated with University of California, Los Angeles, University of California System, Neurobehavioral Systems, Integrative Medicine Institute, University of Colorado Denver

Biochemistry, Genetics and Molecular BiologyPsychology

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: “Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients”.

Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients

Science Advances(2020)10.1126/sciadv.abc9207
N/A
0.691DataRank · unranked
99 citations

Dong Li, Samuel G. Cox, Dylan M. Marchione, Evan F. Joiner, Khadija Wilson +95 more

Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

Genetics in Medicine(2021)10.1038/s41436-021-01152-7
N/A
0.515DataRank · unranked
30 citations

Georgi Stoyanov, Florian Erger, Constantine A. Stratakis, Nikolaos Settas, Edra London +95 more

Myopathy associated with homozygous PYROXD1 pathogenic variants detected by genome sequencing

Neuropathology(2020)10.1111/neup.12641
N/A
0.360DataRank · unranked
10 citations

Négar Khanlou, Hane Lee, Rebecca Signer, Perry B. Shieh, Johnathan Chen +6 more

Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples

Journal of Genetic Counseling(2021)10.1002/jgc4.1451
N/A
0.241DataRank · unranked
4 citations

Kelly Schoch, Jennifer A. Sullivan, Rebecca C. Spillmann, Heidi Cope, Queenie K.‐G. Tan +5 more

Loss of function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.02.06.578086
N/A
0.165DataRank · unranked
2 citations

Kristy Jay, Alden Y. Huang, Jijun Wan, Sharayu Jangam, Odelia Chorin +23 more

Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder,apraxia, and insensitivity to pain

medRxiv(2020)10.1101/2020.09.10.20190314
N/A
0.104DataRank · unranked
1 citations

Georgi Stoyanov, Florian Erger, Jill A. Rosenfeld, Erin Torti, Chad Haldeman‐Englert +18 more

Cultural, demographic, and other non‐demographic factors associated with cancer genetic counseling patients' appointment accompaniment preferences in the United States

Journal of Genetic Counseling(2024)10.1002/jgc4.1942
N/A
0DataRank · unranked
0 citations

Rita M. Cantor, Mariana Niell‐Swiller, Philip Sayegh, Christina G.S. Palmer, Jonathan Lin

Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice

Journal of Genetic Counseling(2020)10.1002/jgc4.1329
N/A
0DataRank · unranked
7 citations

Emily Glanton, Undiagnosed Diseases Network, Janet S. Sinsheimer, Christina G.S. Palmer, Kimberly LeBlanc +1 more

Expansion of NEUROD2 phenotypes to include developmental delay without seizures

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62064
N/A
0DataRank · unranked
11 citations

Annalisa G. Sega, Rebecca Signer, Tracy Cartwright, Weizhen Ji, Julián A. Martínez-Agosto +12 more

Novel NUDT2 variant causes intellectual disability and polyneuropathy

Annals of Clinical and Translational Neurology(2020)10.1002/acn3.51209
N/A
0DataRank · unranked
10 citations

Shaweta Khosa, Dmitriy Niyazov, Hane Lee, Richard Person, Michelle M. Morrow +14 more