Kenneth H. Kraemer

Also affiliated with Department of Health and Human Services

Biochemistry, Genetics and Molecular BiologyMedicine

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 13 papers. Top paper: “Thyroid nodules in xeroderma pigmentosum patients: a feature of premature aging”.

Thyroid nodules in xeroderma pigmentosum patients: a feature of premature aging

Journal of Endocrinological Investigation(2020)10.1007/s40618-020-01451-x

N/A

0DataRank · unranked

10 citations

Jamie Marko, Deborah Tamura, Sikandar G. Khan, Chyi‐Chia Richard Lee, John J. DiGiovanna +2 more

Xeroderma Pigmentosum: A Model for Human Premature Aging

Journal of Investigative Dermatology(2021)10.1016/j.jid.2020.11.012

N/A

0DataRank · unranked

43 citations

John J. DiGiovanna, Sikandar G. Khan, Deborah Tamura, Jack Jeskey, Kenneth H. Kraemer +1 more

Differences in peripheral neuropathy in xeroderma pigmentosum complementation groups A and D as evaluated by nerve conduction studies

BMC Neurology(2021)10.1186/s12883-021-02414-2

N/A

0DataRank · unranked

6 citations

Paul Sackstein, Deborah Tamura, Martha Quezado, Tianxia Wu, Sikandar G. Khan +6 more

Cockayne syndrome, MEN1, and genomic variants: Exome sequencing is changing our view of the genetic landscape

Pediatric Dermatology(2021)10.1111/pde.14655

N/A

0DataRank · unranked

1 citations

Deborah Tamura, Jenny E. Blau, Sikandar G. Khan, Kenneth H. Kraemer, John J. DiGiovanna +1 more

Xeroderma Pigmentosum Group C Splice Mutation Associated with Autism and Hypoglycinemia

UNC Libraries(2021)10.17615/6ezf-xg77

N/A

0DataRank · unranked

17 citations

Steffen Emmert, Randy J. Legerski, Lei Li, James E. Cleaver, Thomas D. Schneider +6 more

Differences in Peripheral Neuropathy in Xeroderma Pigmentosum Complementation Groups A and D

Research Square(2021)10.21203/rs.3.rs-351476/v1

N/A

0DataRank · unranked

0 citations

Paul Sackstein, Deborah Tamura, Martha Quezado, Tianxia Wu, Sikandar G. Khan +6 more

Debilitating hip degeneration in trichothiodystrophy: Association with ERCC2/XPD mutations, osteosclerosis, osteopenia, coxa valga, contractures, and osteonecrosis

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62962

N/A

0DataRank · unranked

9 citations

Grant Randall, Alexandra Edelman, Rina Allawh, Michael Xiong, Deborah Tamura +7 more

Trichothiodystrophy hair shafts display distinct ultrastructural features

Experimental Dermatology(2022)10.1111/exd.14614

N/A

0DataRank · unranked

3 citations

Sikandar G. Khan, Deborah Tamura, John J. DiGiovanna, E. Rizza, Kenneth H. Kraemer +2 more

Retrospective study of efficacy and adverse events of immune checkpoint inhibitors in 22 xeroderma pigmentosum patients with metastatic or unresectable cancers

Frontiers in Oncology(2023)10.3389/fonc.2023.1282823

N/A

0DataRank · unranked

13 citations

Deborah Tamura, Sikandar G. Khan, Sophie Momen, Hiva Fassihi, Robert Sarkany +3 more

Different germline variants in the XPA gene are associated with severe, intermediate, or mild neurodegeneration in xeroderma pigmentosum patients

PLoS Genetics(2024)10.1371/journal.pgen.1011265

N/A

0DataRank · unranked

2 citations

Sikandar G. Khan, Kyoko Imoto, Deborah Tamura, Kyu‐Seon Oh, John J. DiGiovanna +2 more

Personalized sun protection equation: Dermatology + Psychology = XPAND

British Journal of Dermatology(2024)10.1093/bjd/ljae446

N/A

0DataRank · unranked

0 citations

Deborah Tamura, Kenneth H. Kraemer

Co-infection of HSV-1 amplicons containing the XPC gene and a human artificial chromosome vector into primary XPC deficient fibroblast cells

Biochemistry and Biophysics Reports(2024)10.1016/j.bbrep.2024.101875

N/A

0DataRank · unranked

0 citations

Avi Smith, Jonathan A. Garlick, Kenneth H. Kraemer, Zoia L. Monaco, Daniela Moralli

RNA Lariat-Debranching Enzyme (DBR1) Variations in Sabinas Brittle Hair Syndrome Form of Trichothiodystrophy: A Trichothiodystrophy-Causing Gene

Journal of Investigative Dermatology(2025)10.1016/j.jid.2025.06.1591

N/A

0DataRank · unranked

2 citations

Wenelia Baghoomian, Christiane Kuschal-Tauzon, Deborah Tamura, Maxwell P. Lee, John J. DiGiovanna +4 more