Hanoch Slor

Professor

Associate Professor (Emeritus), Faculty of Medicine, NY American Medicine Program
Associate Professor (Emeritus), Faculty of Medicine, Eye Institute (Goldschleger)

Former affiliations

Associate Professor, Faculty of Medicine, Eye Institute (Goldschleger)
Associate Professor, Faculty of Medicine, NY American Medicine Program

Research activity per year

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Dive into the research topics where Hanoch Slor is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

1 Similar Profiles

85 Article
2 Review article
1 Editorial

Clinical utility gene card for: Xeroderma pigmentosum
Schubert, S., Lehmann, J., Kalfon, L., Slor, H., Falik-Zaccai, T. C. & Emmert, S., Jul 2014, In: European Journal of Human Genetics. 22, 7, p. 953 1 p.
Research output: Contribution to journal › Article › peer-review

Open Access

23 Scopus citations
A novel XPD mutation in a compound heterozygote; the mutation in the second allele is present in three homozygous patients with mild sun sensitivity
Falik-Zaccai, T. C., Erel-Segal, R., Horev, L., Bitterman-Deutsch, O., Koka, S., Chaim, S., Keren, Z., Kalfon, L., Gross, B., Segal, Z., Orgal, S., Shoval, Y., Slor, H., Spivak, G. & Hanawalt, P. C., Aug 2012, In: Environmental and Molecular Mutagenesis. 53, 7, p. 505-514 10 p.
Research output: Contribution to journal › Article › peer-review
12 Scopus citations
Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair
Nakazawa, Y., Sasaki, K., Mitsutake, N., Matsuse, M., Shimada, M., Nardo, T., Takahashi, Y., Ohyama, K., Ito, K., Mishima, H., Nomura, M., Kinoshita, A., Ono, S., Takenaka, K., Masuyama, R., Kudo, T., Slor, H., Utani, A., Tateishi, S. & Yamashita, S. & 4 others, Stefanini, M., Lehmann, A. R., Yoshiura, K. I. & Ogi, T., May 2012, In: Nature Genetics. 44, 5, p. 586-592 7 p.
Research output: Contribution to journal › Article › peer-review

Open Access
183 Scopus citations
The versatile DNA nucleotide excision repair (NER) and its medical significance
Falik-Zaccai, T. C., Keren, Z. & Slor, H., Dec 2009, In: Pediatric Endocrinology Reviews. 7, 2, p. 37-42 6 p.
Research output: Contribution to journal › Review article › peer-review
4 Scopus citations
Cockayne syndrome type II in a Druze isolate in Northern Israel in association with an insertion mutation in ERCC6
Falik-Zaccai, T. C., Laskar, M., Kfir, N., Nasser, W., Slor, H. & Khayat, M., 1 Jun 2008, In: American Journal of Medical Genetics, Part A. 146, 11, p. 1423-1429 7 p.
Research output: Contribution to journal › Article › peer-review
29 Scopus citations

Hanoch Slor

Fingerprint

Research output

Clinical utility gene card for: Xeroderma pigmentosum

A novel XPD mutation in a compound heterozygote; the mutation in the second allele is present in three homozygous patients with mild sun sensitivity

Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair

The versatile DNA nucleotide excision repair (NER) and its medical significance

Cockayne syndrome type II in a Druze isolate in Northern Israel in association with an insertion mutation in ERCC6