Results 51 to 60 of about 204 (76)

Fragile X-Associated Neuropsychiatric Disorders (FXAND) in Young Fragile X Premutation Carriers

, 2023
Aishworiya, Ramkumar,; Protic, Dragana,; Tang, Si Jie,; Schneider, Andrea,; Tassone, Flora,; Hagerman, Randi,
core  

Reduced Respiratory Sinus Arrhythmia in Infants with the FMR1 Premutation. [PDF]

Int J Mol Sci
Chase A, Hamrick L, Arnold H, Smith J, Hantman R, Cortez K, Adayev T, Tortora ND, Dahlman A, Roberts J.   +9 more
europepmc   +1 more source

Healthcare Experiences of African American Women with the Fragile X Premutation. [PDF]

J Racial Ethn Health Disparities
King AP, Ali N, Bellcross C, Ehivet F, Hipp HS, Vaughn J, Allen EG.   +6 more
europepmc   +1 more source

Unmethylated Mosaic Full Mutation Males without Fragile X Syndrome. [PDF]

Genes (Basel)
Tak Y, Schneider A, Santos E, Randol JL, Tassone F, Hagerman P, Hagerman RJ.   +6 more
europepmc   +1 more source

Population-based FMR1 carrier screening among reproductive women. [PDF]

J Assist Reprod Genet
Ain Q, Hwang YH, Yeung D, Panpaprai P, Iamurairat W, Chutimongkonkul W, Trachoo O, Tassone F, Jiraanont P.   +8 more
europepmc   +1 more source

Advancing mental health and well-being of Nigerian children through public health screening for Fragile X disorders (CHAMP-FX): protocol of a prospective multicentre screening study with longitudinal follow-up. [PDF]

PLoS One
Mbachu CNP, Eseigbe EE, Mbachu II, Eleje GU, Udigwe IB, Onwuwamah C, Iloghalu IC, Onu J, Manafa OP, Okonkwo O, Adamu H, Aliu R, Ndukwu CI, Ndubuisi VU, Ogholaja TE, Ilikannu SO, Mbanuzuru A, Anukam K, Olorunfemi G, Odita AO, Echezona DM, Okereke U, Umeadi E, Udigwe GO, Bayo AU, Elo-Ilo J, Idume MR, Ezeudu CE, Odinaka K, Ezeno ZC, Ofojebe B, Obiegbu A, Onyejiaka C, Egbogu A, Azubike OC, Okeke NC, Ugochukwu EN, Oriji SO, Ezeuko YA, Adeniyi UP, Okafor LU, Ebenebe JC, Richard U, Ezechukwu CC, Tassone F, Hagerman R.   +45 more
europepmc   +1 more source

Improving women's healthcare providers' knowledge about fragile X-associated primary ovarian insufficiency through a novel educational tool. [PDF]

J Assist Reprod Genet
Peery E, Singleton AL, Merkison J, Brockman D, Hipp H, Ali N, Lichten L, Allen EG.   +7 more
europepmc   +1 more source

Aberrant Short Tandem Repeats: Pathogenicity, Mechanisms, Detection, and Roles in Neuropsychiatric Disorders. [PDF]

Genes (Basel)
Liu Y, Xia K.
europepmc   +1 more source

Personalized Follow Up and Genetic Diagnosis Update of FMR1-Related Conditions: A Change in Diagnosis, Prognosis and Expectations. [PDF]

Int J Mol Sci
Roche-Martínez A, Ramírez-Mallafré A, Joga-Elvira L, Manso-Bazus C, Rubio-Roy M, Baena-Diez N.   +5 more
europepmc   +1 more source

Prevalence of fragile X syndrome in South Asia, and importance of diagnosis. [PDF]

Med Rev (2021)
Fazna A, Hagerman RJ.
europepmc   +1 more source