PubMed (Bookshelf cited) for id: 6915

Year	Number of Results
1996	1
1998	2
1999	2
2000	3
2001	4
2002	4
2003	1
2004	1
2006	2
2007	1
2008	5
2009	2
2010	5
2011	2
2012	2
2013	4
2014	3
2015	9
2016	4
2017	6
2018	6
2019	1
2022	1
2024	0

1

Variation among DNA banking consent forms: points for clinicians to bank on.

Huang SJ, Amendola LM, Sternen DL. Huang SJ, et al. J Community Genet. 2022 Aug;13(4):389-397. doi: 10.1007/s12687-022-00601-3. Epub 2022 Jul 14. J Community Genet. 2022. PMID: 35834113 Free PMC article.

2

Heterogeneity of clinical features and mutation analysis of NTRK1 in Han Chinese patients with congenital insensitivity to pain with anhidrosis.

Li N, Guo S, Wang Q, Duan G, Sun J, Liu Y, Zhang J, Wang C, Zhu C, Liu J, Zhang X. Li N, et al. J Pain Res. 2019 Jan 22;12:453-465. doi: 10.2147/JPR.S188566. eCollection 2019. J Pain Res. 2019. PMID: 30774415 Free PMC article.

3

A third HSAN5 mutation disrupts the nerve growth factor furin cleavage site.

Shaikh SS, Nahorski MS, Woods CG. Shaikh SS, et al. Mol Pain. 2018 Jan-Dec;14:1744806918809223. doi: 10.1177/1744806918809223. Epub 2018 Oct 8. Mol Pain. 2018. PMID: 30296891 Free PMC article.

4

Congenital Loss of Permanent Teeth in a Patient With Congenital Insensitivity to Pain With Anhidrosis due to 2 Novel Mutations in the NTRK1 Gene.

Xue XM, Liu YQ, Pang P, Sun CF. Xue XM, et al. J Oral Maxillofac Surg. 2018 Dec;76(12):2582.e1-2582.e9. doi: 10.1016/j.joms.2018.06.170. Epub 2018 Jul 7. J Oral Maxillofac Surg. 2018. PMID: 30075136

5

Novel NTRK1 mutations in Chinese patients with congenital insensitivity to pain with anhidrosis.

Geng X, Liu Y, Ren X, Guan Y, Wang Y, Mao B, Zhao X, Zhang X. Geng X, et al. Mol Pain. 2018 Jan-Dec;14:1744806918781140. doi: 10.1177/1744806918781140. Epub 2018 May 17. Mol Pain. 2018. PMID: 29770739 Free PMC article.

6

NGF-dependent neurons and neurobiology of emotions and feelings: Lessons from congenital insensitivity to pain with anhidrosis.

Indo Y. Indo Y. Neurosci Biobehav Rev. 2018 Apr;87:1-16. doi: 10.1016/j.neubiorev.2018.01.013. Epub 2018 Feb 20. Neurosci Biobehav Rev. 2018. PMID: 29407522 Free article. Review.

7

A novel human pain insensitivity disorder caused by a point mutation in ZFHX2.

Habib AM, Matsuyama A, Okorokov AL, Santana-Varela S, Bras JT, Aloisi AM, Emery EC, Bogdanov YD, Follenfant M, Gossage SJ, Gras M, Humphrey J, Kolesnikov A, Le Cann K, Li S, Minett MS, Pereira V, Ponsolles C, Sikandar S, Torres JM, Yamaoka K, Zhao J, Komine Y, Yamamori T, Maniatis N, Panov KI, Houlden H, Ramirez JD, Bennett DLH, Marsili L, Bachiocco V, Wood JN, Cox JJ. Habib AM, et al. Brain. 2018 Feb 1;141(2):365-376. doi: 10.1093/brain/awx326. Brain. 2018. PMID: 29253101 Free PMC article.

8

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

9

Sodium channel NaV1.9 mutations associated with insensitivity to pain dampen neuronal excitability.

Huang J, Vanoye CG, Cutts A, Goldberg YP, Dib-Hajj SD, Cohen CJ, Waxman SG, George AL Jr. Huang J, et al. J Clin Invest. 2017 Jun 30;127(7):2805-2814. doi: 10.1172/JCI92373. Epub 2017 May 22. J Clin Invest. 2017. PMID: 28530638 Free PMC article.

10

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.

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