Search Results - Booth, Kevin

Kevin Booth

Kevin Booth (born October 2, 1961) is an American film director, producer, lecturer and musician. He was known for his documentary film series ''American Drug War''. Booth worked with comedian Bill Hicks, until the time of his death on February 26, 1994 and posthumously produced Hicks' records ''Rant in E Minor'' and ''Arizona Bay''.

Booth also explored controversial subjects such as the Waco siege and the New World Order. Booth lectures at universities while continuing to make more films about American drug policy. Provided by Wikipedia
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  1. 1
    DFNA5 (GSDME) c.991-15_991-13delTTC: Founder Mutation or Mutational Hotspot?

    DFNA5 (GSDME) c.991-15_991-13delTTC: Founder Mutation or Mutational Hotspot? by Booth, Kevin T., Azaiez, Hela, Smith, Richard J. H.

    Published 2020
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  2. 2
    Old gene, new phenotype: Splicing altering variants in CEACAM16 cause recessive non-syndromic hearing impairment

    Old gene, new phenotype: Splicing altering variants in CEACAM16 cause recessive non-syndromic hearing impairment by Booth, Kevin T, Kahrizi, Kimia, Najmabadi, Hossein, Azaiez, Hela, Smith, Richard J

    Published 2018
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  3. 3
    Intracellular Regulome Variability Along the Organ of Corti: Evidence, Approaches, Challenges, and Perspective

    Intracellular Regulome Variability Along the Organ of Corti: Evidence, Approaches, Challenges, and Perspective by Booth, Kevin T., Azaiez, Hela, Jahan, Israt, Smith, Richard J. H., Fritzsch, Bernd

    Published 2018
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  4. 4
    Identification of Novel and Recurrent Variants in MYO15A in Ashkenazi Jewish Patients With Autosomal Recessive Nonsyndromic Hearing Loss

    Identification of Novel and Recurrent Variants in MYO15A in Ashkenazi Jewish Patients With Autosomal Recessive Nonsyndromic Hearing Loss by Booth, Kevin T., Hirsch, Yoel, Vardaro, Anna C., Ekstein, Josef, Yefet, Devorah, Quint, Adina, Weiden, Tzvi, Corey, David P.

    Published 2021
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  5. 5
    Exonic mutations and exon skipping: lessons learned from DFNA5

    Exonic mutations and exon skipping: lessons learned from DFNA5 by Booth, Kevin T, Azaiez, Hela, Kahrizi, Kimia, Wang, Donghong, Zhang, Yuzhou, Frees, Kathy, Nishimura, Carla, Najmabadi, Hossein, Smith, Richard J

    Published 2018
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  6. 6
    Mutations in LOXHD1 gene cause various types and severities of hearing loss

    Mutations in LOXHD1 gene cause various types and severities of hearing loss by Mori, Kentaro, Moteki, Hideaki, Kobayashi, Yumiko, Azaiez, Hela, Booth, Kevin T, Nishio, Shin-ya, Sato, Hiroaki, Smith, Richard J H, Usami, Shin-ichi

    Published 2015
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  7. 7
    Defective Tmprss3-Associated Hair Cell Degeneration in Inner Ear Organoids

    Defective Tmprss3-Associated Hair Cell Degeneration in Inner Ear Organoids by Tang, Pei-Ciao, Alex, Alpha L., Nie, Jing, Lee, Jiyoon, Roth, Adam A., Booth, Kevin T., Koehler, Karl R., Hashino, Eri, Nelson, Rick F.

    Published 2019
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  8. 8
    TBC1D24 Mutation Causes Autosomal Dominant Non-Syndromic Hearing Loss

    TBC1D24 Mutation Causes Autosomal Dominant Non-Syndromic Hearing Loss by Azaiez, Hela, Booth, Kevin T., Bu, Fengxiao, Huygen, Patrick, Shibata, Seiji, Shearer, A. Eliot, Kolbe, Diana, Meyer, Nicole, Black-Ziegelbein, E. Ann, Smith, Richard J.H.

    Published 2014
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  9. 9
    De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing loss

    De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing loss by Moteki, Hideaki, Shearer, A Eliot, Izumi, Shuji, Kubota, Yamato, Azaiez, Hela, Booth, Kevin T, Sloan, Christina M, Kolbe, Diana L, Smith, Richard JH, Usami, Shin-ichi

    Published 2015
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  10. 10
    USH2 caused by GPR98 mutation diagnosed by massively parallel sequencing in advance of the occurrence of visual symptoms

    USH2 caused by GPR98 mutation diagnosed by massively parallel sequencing in advance of the occurrence of visual symptoms by Moteki, Hideaki, Yoshimura, Hidekane, Azaiez, Hela, Booth, Kevin T., Shearer, A Eliot, Sloan, Christina M., Kolbe, Diana L., Murata, Toshinori, Smith, Richard J. H., Usami, Shin-ichi

    Published 2015
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  11. 11
    Comprehensive genetic testing with ethnic-specific filtering by allele frequency in a Japanese hearing-loss population

    Comprehensive genetic testing with ethnic-specific filtering by allele frequency in a Japanese hearing-loss population by Moteki, Hideaki, Azaiez, Hela, Booth, Kevin T, Shearer, A Eliot, Sloan, Christina M, Kolbe, Diana L, Nishio, Shin-ya, Hattori, Mitsuru, Usami, Shin-ichi, Smith, Richard J H

    Published 2015
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  12. 12
    Long-Term Extensions of Randomized Vaccination Trials of ACC-001 and QS-21 in Mild to Moderate Alzheimer’s Disease

    Long-Term Extensions of Randomized Vaccination Trials of ACC-001 and QS-21 in Mild to Moderate Alzheimer’s Disease by Hüll, Michael, Sadowsky, Carl, Arai, Heii, Leterme, Ghislaine Le Prince, Holstein, Ann, Booth, Kevin, Peng, Yahong, Yoshiyama, Tamotsu, Suzuki, Hideo, Ketter, Nzeera, Liu, Enchi, Ryan, J. Michael

    Published 2017
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  13. 13
    Long-term safety and tolerability of bapineuzumab in patients with Alzheimer’s disease in two phase 3 extension studies

    Long-term safety and tolerability of bapineuzumab in patients with Alzheimer’s disease in two phase 3 extension studies by Ivanoiu, Adrian, Pariente, Jérémie, Booth, Kevin, Lobello, Kasia, Luscan, Gerald, Hua, Lisa, Lucas, Prisca, Styren, Scot, Yang, Lingfeng, Li, David, Black, Ronald S., Brashear, H. Robert, McRae, Thomas

    Published 2016
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  14. 14
    Variants in CIB2 cause DFNB48 and not USH1J

    Variants in CIB2 cause DFNB48 and not USH1J by Booth, Kevin T, Kahrizi, Kimia, Babanejad, Mojgan, Daghagh, Hossein, Bademci, Guney, Arzhangi, Sanaz, Zareabdollahi, Davood, Duman, Duygu, El-Amraoui, Aziz, Tekin, Mustafa, Najmabadi, Hossein, Azaiez, Hela, Smith, Richard J

    Published 2018
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  15. 15
    Novel Loss-of-Function Mutations in COCH Cause Autosomal Recessive Nonsyndromic Hearing Loss

    Novel Loss-of-Function Mutations in COCH Cause Autosomal Recessive Nonsyndromic Hearing Loss by Booth, Kevin T, Ghaffar, Amama, Rashid, Muhammad, Hovey, Luke T, Hussain, Mureed, Frees, Kathy, Renkes, Erika M, Nishimura, Carla J, Shahzad, Mohsin, Smith, Richard J, Ahmed, Zubair, Azaiez, Hela, Riazuddin, Saima

    Published 2020
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  16. 16
    Hearing loss caused by a P2RX2 mutation identified in a MELAS family with a coexisting mitochondrial 3243AG mutation

    Hearing loss caused by a P2RX2 mutation identified in a MELAS family with a coexisting mitochondrial 3243AG mutation by Moteki, Hideaki, Azaiez, Hela, Booth, Kevin T, Hattori, Mitsuru, Sato, Ai, Sato, Yoshihiko, Motobayashi, Mitsuo, Sloan, Christina M, Kolbe, Diana L, Shearer, A Eliot, Smith, Richard J H, Usami, Shin-ichi

    Published 2015
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  17. 17
    When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS)

    When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS) by Mohseni, Marzieh, Akbari, Mojdeh, Booth, Kevin T, Babanejad, Mojgan, Azaiez, Hela, Ardalani, Fariba, Arzhangi, Sanaz, Jalalvand, Khadijeh, Nikzat, Nooshin, Ghodratpour, Fatemeh, jamali, payman, Adeli, Omid Ali, Habibi, Haleh, Kahrizi, Kimia, Najmabadi, Hossein

    Published 2020
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  18. 18
    Detection and confirmation of deafness-causing copy number variations in the STRC gene by massively parallel sequencing and comparative genomic hybridization

    Detection and confirmation of deafness-causing copy number variations in the STRC gene by massively parallel sequencing and comparative genomic hybridization by Moteki, Hideaki, Azaiez, Hela, Sloan-Heggen, Christina M, Booth, Kevin, Nishio, Shin-ya, Wakui, Keiko, Yamaguchi, Tomomi, Kolbe, Diana L, Iwasa, Yoh-ichiro, Shearer, A Eliot, Fukushima, Yoshimitsu, Smith, Richard JH, Usami, Shin-ichi

    Published 2016
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  19. 19
    Novel PTPRQ mutations identified in three congenital hearing loss patients with various types of hearing loss

    Novel PTPRQ mutations identified in three congenital hearing loss patients with various types of hearing loss by Sakuma, Naoko, Moteki, Hideaki, Azaiez, Hela, Booth, Kevin T, Takahashi, Masahiro, Arai, Yasuhiro, Shearer, A Eliot, Sloan, Christina M, Nishio, Shin-ya, Kolbe, Diana L, Iwasaki, Satoshi, Oridate, Nobuhiko, Smith, Richard J H, Usami, Shin-ichi

    Published 2015
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  20. 20
    Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review

    Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review by Beheshtian, Maryam, Babanejad, Mojgan, Azaiez, Hela, Bazazzadegan, Niloofar, Kolbe, Diana, Sloan-Heggen, Christina, Arzhangi, Sanaz, Booth, Kevin, Mohseni, Marzieh, Frees, Kathy, Hossein Azizi, Mohammad, Daneshi, Ahmad, Farhadi, Mohammad, Kahrizi, Kimia, Smith, Richard JH, Najmabadi, Hossein

    Published 2016
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