Kenneth H Kraemer

10PUBLICATIONS
15CO-AUTHORS
Cancer geneticsMajor global burdens of diseaseEpigenetics (incl. genome methylation and epigenomics)Cancer diagnosisInnate immunity
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Publications (10)

|Dec 02, 2024
Different germline variants in the XPA gene are associated with severe, intermediate, or mild neurodegeneration in xeroderma pigmentosum patients.

Jeffrey P Sagun, Sikandar G Khan, Kyoko Imoto

|Sep 14, 2022
Debilitating hip degeneration in trichothiodystrophy: Association with ERCC2/XPD mutations, osteosclerosis, osteopenia, coxa valga, contractures, and osteonecrosis.

John J DiGiovanna, Grant Randall, Alexandra Edelman

|Jun 09, 2021
Cockayne syndrome, MEN1, and genomic variants: Exome sequencing is changing our view of the genetic landscape.

Sandra R Oska, Deborah Tamura, Jenny E Blau

|Nov 06, 2020
Thyroid nodules in xeroderma pigmentosum patients: a feature of premature aging.

S D Kouatcheu, J Marko, D Tamura

|May 09, 2019
Hydroa vacciniforme-like lymphoproliferative disorder: an EBV disease with a low risk of systemic illness in whites.

Jeffrey I Cohen, Irini Manoli, Kennichi Dowdell

|Jun 14, 2018
Four-dimensional, dynamic mosaicism is a hallmark of normal human skin that permits mapping of the organization and patterning of human epidermis during terminal differentiation.

Yun Wang, Taro Masaki, Sikandar G Khan

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Frequent Collaborators

5 joint publications

John J DiGiovanna

4 joint publications

Sikandar G Khan

2 joint publications

Deborah Tamura

1 joint publications

S D Kouatcheu