Rachel Sayuri Honjo Kawahira (R S Honjo, Rachel Sayuri Honjo, Rachel S Honjo)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 12

Top Topics

Oral Anticoagulants

Aortic Valve Replacement

Top Venues

American journal of medical genetics. Part A

Journal of community genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Fernanda Teresa de Lima, Maria Angélica de Faria Domingues de Lima, Patrícia Santana Correia, Rachel Sayuri Honjo Kawahira, Rayana Elias Maia, Sandra Obikawa Kyosen, Debora Gusmão Melo
Teaching and training of human resources for genetics and genomics in Brazil. Journal of community genetics (2024)
Rebeca Orselli Monteiro, Tally Lichtensztejn Tafla, Juliana Dalla Martha Rodriguez, Sabine Triguero Teixeira, Rachel Sayuri Honjo Kawahira, Chong Ae Kim, Maria Cristina Triguero Veloz Teixeira
Parental attitudes and beliefs about sexuality of individuals with intellectual disability: Insights from a Brazilian sample of parents of individuals with Williams syndrome. Journal of applied research in intellectual disabilities : JARID (2023)
Liliane Aparecida Fagundes Silva, Rachel Sayuri Honjo Kawahira, Chong Ae Kim, Carla Gentile Matas
Audiological profile and cochlear functionality in Williams syndrome. CoDAS 34 (3) (2022)
Taccyanna M Ali, Bianca D W Linnenkamp, Guilherme L Yamamoto, Rachel Sayuri Honjo Kawahira, Hamilton Cabral de Menezes Filho, Chong Ae Kim, Debora Romeo Bertola
The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry. American journal of medical genetics. Part A 188 (5) (2022)
Rachel Sayuri Honjo Kawahira, Matheus Augusto Araujo Castro, Suely Fazio Ferraciolli, Luiz Alberto Valente Soares Junior, Antonio Carlos Pastorino, Debora Romeo Bertola, Noriko Miyake, Naomichi Matsumoto, Chong Ae Kim
Cerebellofaciodental syndrome in an adult patient: Expanding the phenotypic and natural history characteristics. American journal of medical genetics. Part A 185 (5) (2021)
Lucas Vieira Lacerda Pires, Renata de Almeida Bordim, Maria Beatriz Rabelo Maciel, Ana Cristina Sayuri Tanaka, Guilherme Lopes Yamamoto, Rachel Sayuri Honjo Kawahira, Chong Ae Kim, Debora Romeo Bertola
Atypical, severe hypertrophic cardiomyopathy in a newborn presenting Noonan syndrome harboring a recurrent heterozygous MRAS variant. American journal of medical genetics. Part A 185 (10) (2021)
Matheus Augusto Araujo Castro, Juliana Heather Vedovato Dos Santos, Rachel Sayuri Honjo Kawahira, Guilherme Lopes Yamamoto, Debora Romeo Bertola, Anna C E Hurst, Lynn P Chorich, Lawrence C Layman, Chong Ae Kim, Hyung-Goo Kim
Twenty-year follow-up of the facial phenotype of Brazilian patients with Sotos syndrome. American journal of medical genetics. Part A 185 (12) (2021)
Rachel Sayuri Honjo Kawahira, Vanessa Figueiredo Monteleone, Vera Demarchi Aiello, Jaqueline Wagenfuhr, Victor Sarli Issa, Pablo Maria Alberto Pomerantzeff, Erika Arai Furusawa, Evelin Aline Zanardo, Leslie Domenici Kulikowski, Debora Romeo Bertola, Chong Ae Kim
Cardiovascular findings in Williams-Beuren Syndrome: Experience of a single center with 127 cases. American journal of medical genetics. Part A (2021)
Lucas Vieira Lacerda Pires, Rogério Lemos Ribeiro, Adriana Modesto de Sousa, Bianca Domit Werner Linnenkamp, Sue Ellen Pontes, Maria Cristina Triguero Veloz Teixeira, Debora Maria Befi-Lopes, Rachel Sayuri Honjo Kawahira, Debora Romeo Bertola, Chong Ae Kim
Nationwide questionnaire data of 229 Williams-Beuren syndrome patients using WhatsApp tool. Arquivos de neuro-psiquiatria 79 (11) (2021)
Yuri Uchiyama, Daisuke Yamaguchi, Kazuhiro Iwama, Satoko Miyatake, Kohei Hamanaka, Naomi Tsuchida, Hiromi Aoi, Yoshiteru Azuma, Toshiyuki Itai, Ken Saida, Hiromi Fukuda, Futoshi Sekiguchi, Tomohiro Sakaguchi, Ming Lei, Sachiko Ohori, Masamune Sakamoto, Mitsuhiro Kato, Takayoshi Koike, Yukitoshi Takahashi, Koichi Tanda, Yuki Hyodo, Rachel Sayuri Honjo Kawahira, Debora Romeo Bertola, Chong Ae Kim, Masahide Goto, Tetsuya Okazaki, Hiroyuki Yamada, Yoshihiro Maegaki, Hitoshi Osaka, Lock Hock Ngu, Gaik-Siew Ch'ng, Keng W Teik, Manami Akasaka, Hiroshi Doi, Fumiaki Tanaka, Tomohide Goto, Long Guo, Shiro Ikegawa, Kazuhiro Haginoya, Muzhirah Haniffa, Nozomi Hiraishi, Yoko Hiraki, Satoru Ikemoto, Atsuro Daida, Shin-Ichiro Hamano, Masaki Miura, Akihiko Ishiyama, Osamu Kawano, Akane Kondo, Hiroshi Matsumoto, Nobuhiko Okamoto, Tohru Okanishi, Yukimi Oyoshi, Eri Takeshita, Toshifumi Suzuki, Yoshiyuki Ogawa, Hiroshi Handa, Yayoi Miyazono, Eriko Koshimizu, Atsushi Fujita, Atsushi Takata, Noriko Miyake, Takeshi Mizuguchi, Naomichi Matsumoto
Efficient detection of copy-number variations using exome data: Batch- and sex-based analyses. Human mutation 42 (1) (2020)
Rachel Sayuri Honjo Kawahira, Evelyn Cristina Nuñez Vaca, Gabriela Nunes Leal, Deipara Monteiro Abellan, Nana Miura Ikari, Marcelo Biscegli Jatene, Ana Maria Martins, Chong Ae Kim
Mucopolysaccharidosis type VI: case report with first neonatal presentation with ascites fetalis and rapidly progressive cardiac manifestation. BMC medical genetics 21 (1) (2020)
Rachel Sayuri Honjo Kawahira, C B Mello, L S E Pimenta, E C Nuñes-Vaca, L M Benedetto, R B F Khoury, D M Befi-Lopes, C A Kim
Cri du Chat syndrome: Characteristics of 73 Brazilian patients. Journal of intellectual disability research : JIDR 62 (6) (2018)