DNA methylation epi-signature and biological age in attention deficit hyperactivity disorder patients
Carvalho, Gleyson Francisco da Silva, Costa, Thais Virginia Moura Machado, Nascimento, Amom Mendes, Wolff, Beatriz Martins, Damasceno, Julian Gabriel, Vieira, Lucas Liro, Almeida, Vanessa Tavares, Oliveira, Yanca Gasparini de, Mello, Claudia Berlim de, Muszkat, Mauro, Kulikowski, Leslie Domenici
Published in Clinical neurology and neurosurgery (01.05.2023)
Published in Clinical neurology and neurosurgery (01.05.2023)
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Journal Article
Differences in DNA methylation status explain phenotypic variability in patients with 5p- syndrome
Almeida, Vanessa Tavares, Chehimi, Samar N, Carvalho, Gleyson F S, Gasparini, Yanca, Nascimento, Amom M, Vieira, Lucas L, Wolff, Beatriz M, Montenegro, Marília M, Kulikowski, Leslie D
Published in BMC research notes (29.04.2024)
Published in BMC research notes (29.04.2024)
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Journal Article
Novel rearrangements between different chromosomes with direct impact on the diagnosis of 5p- syndrome
Chehimi, Samar Nasser, Almeida, Vanessa Tavares, Nascimento, Amom Mendes, Zanardo, Évelin Aline, de Oliveira, Yanca Gasparini, Carvalho, Gleyson Francisco da Silva, Wolff, Beatriz Martins, Montenegro, Marilia Moreira, de Assunção, Nilson Antônio, Kim, Chong Ae, Kulikowski, Leslie Domenici
Published in Clinics (São Paulo, Brazil) (01.01.2022)
Published in Clinics (São Paulo, Brazil) (01.01.2022)
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Journal Article
The complex search for the cause of gastroschisis
de Freitas, Amanda Brasil, Francisco, Rossana Pulcineli Vieira, Hoshida, Mara Sandra, De Oliveira, Yanca Gasparini, Kulikowski, Leslie Domenici, de Lourdes Brizot, Maria
Published in Birth defects research (15.11.2022)
Published in Birth defects research (15.11.2022)
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Journal Article
Gene expression profile suggesting immunological dysregulation in two Brazilian Bloom's syndrome cases
Montenegro, Marilia M., Quaio, Caio R., Palmeira, Patricia, Gasparini, Yanca, Rangel‐Santos, Andreia, Damasceno, Julian, Novak, Estela M., Gimenez, Thamires M., Yamamoto, Guilherme L., Ronjo, Rachel S., Novo‐Filho, Gil M., Chehimi, Samar N., Zanardo, Evelin A., Dias, Alexandre T., Nascimento, Amom M., Costa, Thais V. M. M., Duarte, Alberto J. da S., Coutinho, Luiz L., Kim, Chong A., Kulikowski, Leslie D.
Published in Molecular genetics & genomic medicine (01.04.2020)
Published in Molecular genetics & genomic medicine (01.04.2020)
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Breakpoint delineation in 5p‐ patients leads to new insights about microcephaly and the typical high‐pitched cry
Chehimi, Samar N., Zanardo, Évelin A., Ceroni, José R. M., Nascimento, Amom M., Madia, Fabrícia A. R., Dias, Alexandre T., Filho, Gil M. N., Montenegro, Marília M., Damasceno, Jullian, Costa, Thaís V. M. M., Gasparini, Yanca, Kim, Chong A., Kulikowski, Leslie D.
Published in Molecular genetics & genomic medicine (01.02.2020)
Published in Molecular genetics & genomic medicine (01.02.2020)
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Journal Article
Expanding the Phenotype of 8p23.1 Deletion Syndrome: Eight New Cases Resembling the Clinical Spectrum of 22q11.2 Microdeletion
Montenegro, Marília Moreira, Camilotti, Débora, Quaio, Caio Robledo D’Anglioli Costa, Gasparini, Yanca, Zanardo, Évelin Aline, Rangel-Santos, Andreia, Novo-Filho, Gil Monteiro, Francisco, Gleyson, Liro, Lucas, Nascimento, Amom, Chehimi, Samar Nasser, Soares, Diogo Cordeiro Queiroz, Krepischi, Ana C.V., Grassi, Marcília Sierro, Honjo, Rachel Sayuri, Palmeira, Patricia, Kim, Chong Ae, Carneiro-Sampaio, Magda Maria Sales, Rosenberg, Carla, Kulikowski, Leslie Domenici
Published in The Journal of pediatrics (01.01.2023)
Published in The Journal of pediatrics (01.01.2023)
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Journal Article
Mosaic Trisomy 12 Associated with Overgrowth Detected in Fibroblast Cell Lines
Gasparini, Yanca, Montenegro, Marília M, Novo-Filho, Gil M, Ceroni, José R M, Honjo, Rachel S, Zanardo, Évelin A, Dias, Alexandre T, Nascimento, Amon M, Costa, Taís V M M, Madia, Fabrícia A, Chehimi, Samar N, Damasceno, Jullian G, Kim, Chong A, Kulikowski, Leslie D
Published in Cytogenetic and genome research (01.01.2019)
Published in Cytogenetic and genome research (01.01.2019)
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Journal Article
Cri-du-Chat Syndrome: Revealing a Familial Atypical Deletion in 5p
Almeida, Vanessa T., Chehimi, Samar N., Gasparini, Yanca, Nascimento, Amom M., Carvalho, Gleyson F.S., Montenegro, Marília M., Zanardo, Évelin Aline, Dias, Alexandre T., Assunção, Nilson A., Kim, Chong A., Kulikowski, Leslie D.
Published in Molecular syndromology (01.01.2023)
Published in Molecular syndromology (01.01.2023)
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Journal Article
Cri-du-Chat Syndrome: Revealing a Familial Atypical Deletion in 5p
Almeida, Vanessa T, Chehimi, Samar N, Gasparini, Yanca, Nascimento, Amom M, Carvalho, Gleyson F S, Montenegro, Marília M, Zanardo, Évelin Aline, Dias, Alexandre T, Assunção, Nilson A, Kim, Chong A, Kulikowski, Leslie D
Published in Molecular syndromology (01.01.2023)
Published in Molecular syndromology (01.01.2023)
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