PubMed (Bookshelf cited) for id: 12147

Year	Number of Results
1996	1
1997	1
1999	1
2003	1
2010	2
2011	2
2012	1
2013	4
2014	3
2016	2
2017	5
2018	1
2019	2
2020	4
2021	4
2024	0

1

Management guideline for Werner syndrome 2020 1. Dyslipidemia and fatty liver associated with Werner syndrome.

Tsukamoto K, Takemoto M, Kubota Y, Taniguchi T, Motegi SI, Taniguchi A, Nakagami H, Maezawa Y, Koshizaka M, Kato H, Mori S, Kuzuya M, Yokote K. Tsukamoto K, et al. Geriatr Gerontol Int. 2021 Feb;21(2):133-138. doi: 10.1111/ggi.14095. Epub 2020 Dec 1. Geriatr Gerontol Int. 2021. PMID: 33258561

2

Management guideline for Werner syndrome 2020. 6. Skin ulcers associated with Werner syndrome: Prevention and non-surgical and surgical treatment.

Kubota Y, Takemoto M, Taniguchi T, Motegi SI, Taniguchi A, Nakagami H, Maezawa Y, Koshizaka M, Kato H, Mori S, Tsukamoto K, Kuzuya M, Yokote K. Kubota Y, et al. Geriatr Gerontol Int. 2021 Feb;21(2):153-159. doi: 10.1111/ggi.14096. Epub 2020 Nov 22. Geriatr Gerontol Int. 2021. PMID: 33225552

3

Management guideline for Werner syndrome 2020. 3. Diabetes associated with Werner syndrome.

Takemoto M, Kubota Y, Taniguchi T, Motegi SI, Taniguchi A, Nakagami H, Maezawa Y, Koshizaka M, Kato H, Tsukamoto K, Mori S, Kuzuya M, Yokote K. Takemoto M, et al. Geriatr Gerontol Int. 2021 Feb;21(2):142-145. doi: 10.1111/ggi.14083. Epub 2020 Nov 9. Geriatr Gerontol Int. 2021. PMID: 33169495

4

Management guideline for Werner syndrome 2020. 4. Osteoporosis associated with Werner syndrome.

Mori S, Takemoto M, Kubota Y, Taniguchi T, Motegi SI, Taniguchi A, Nakagami H, Maezawa Y, Koshizaka M, Kato H, Tsukamoto K, Kuzuya M, Yokote K. Mori S, et al. Geriatr Gerontol Int. 2021 Feb;21(2):146-149. doi: 10.1111/ggi.14078. Epub 2020 Nov 5. Geriatr Gerontol Int. 2021. PMID: 33155383 No abstract available.

5

2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines.

Arnett DK, Blumenthal RS, Albert MA, Buroker AB, Goldberger ZD, Hahn EJ, Himmelfarb CD, Khera A, Lloyd-Jones D, McEvoy JW, Michos ED, Miedema MD, Muñoz D, Smith SC Jr, Virani SS, Williams KA Sr, Yeboah J, Ziaeian B. Arnett DK, et al. Circulation. 2019 Sep 10;140(11):e596-e646. doi: 10.1161/CIR.0000000000000678. Epub 2019 Mar 17. Circulation. 2019. PMID: 30879355 Free PMC article. Review. No abstract available.

6

The ophthalmic diagnosis and management of four siblings with Werner syndrome.

Lyons C, Gallagher D, McSwiney T, McElnea E, Kinsella F. Lyons C, et al. Int Ophthalmol. 2019 Jun;39(6):1371-1378. doi: 10.1007/s10792-018-0929-8. Epub 2018 Apr 28. Int Ophthalmol. 2019. PMID: 29705892

7

Parental influence on human germline de novo mutations in 1,548 trios from Iceland.

Jónsson H, Sulem P, Kehr B, Kristmundsdottir S, Zink F, Hjartarson E, Hardarson MT, Hjorleifsson KE, Eggertsson HP, Gudjonsson SA, Ward LD, Arnadottir GA, Helgason EA, Helgason H, Gylfason A, Jonasdottir A, Jonasdottir A, Rafnar T, Frigge M, Stacey SN, Th Magnusson O, Thorsteinsdottir U, Masson G, Kong A, Halldorsson BV, Helgason A, Gudbjartsson DF, Stefansson K. Jónsson H, et al. Nature. 2017 Sep 28;549(7673):519-522. doi: 10.1038/nature24018. Epub 2017 Sep 20. Nature. 2017. PMID: 28959963

8

The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies.

Stenson PD, Mort M, Ball EV, Evans K, Hayden M, Heywood S, Hussain M, Phillips AD, Cooper DN. Stenson PD, et al. Hum Genet. 2017 Jun;136(6):665-677. doi: 10.1007/s00439-017-1779-6. Epub 2017 Mar 27. Hum Genet. 2017. PMID: 28349240 Free PMC article. Review.

9

Homozygosity for the WRN Helicase-Inactivating Variant, R834C, does not confer a Werner syndrome clinical phenotype.

Kamath-Loeb AS, Zavala-van Rankin DG, Flores-Morales J, Emond MJ, Sidorova JM, Carnevale A, Cárdenas-Cortés MD, Norwood TH, Monnat RJ, Loeb LA, Mercado-Celis GE. Kamath-Loeb AS, et al. Sci Rep. 2017 Mar 9;7:44081. doi: 10.1038/srep44081. Sci Rep. 2017. PMID: 28276523 Free PMC article. Clinical Trial.

10

WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects.

Yokote K, Chanprasert S, Lee L, Eirich K, Takemoto M, Watanabe A, Koizumi N, Lessel D, Mori T, Hisama FM, Ladd PD, Angle B, Baris H, Cefle K, Palanduz S, Ozturk S, Chateau A, Deguchi K, Easwar TK, Federico A, Fox A, Grebe TA, Hay B, Nampoothiri S, Seiter K, Streeten E, Piña-Aguilar RE, Poke G, Poot M, Posmyk R, Martin GM, Kubisch C, Schindler D, Oshima J. Yokote K, et al. Hum Mutat. 2017 Jan;38(1):7-15. doi: 10.1002/humu.23128. Epub 2016 Oct 7. Hum Mutat. 2017. PMID: 27667302 Free PMC article. Review.

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