The health risks of ART

von Grafodatskaya, Daria, Cytrynbaum, Cheryl, Weksberg, Rosanna
Veröffentlicht 2013

Beckwith–Wiedemann syndrome

von Weksberg, Rosanna, Shuman, Cheryl, Beckwith, J Bruce
Veröffentlicht 2010

Velo-Cardio-Facial Syndrome and Psychotic Disorders: Implications for Psychiatric Genetics

von Chow, Eva W.C., Bassett, Anne S., Weksberg, Rosanna
Veröffentlicht 1994

Chromosomal Abnormalities and Schizophrenia

von BASSETT, ANNE S., CHOW, EVA W.C., WEKSBERG, ROSANNA
Veröffentlicht 2000

An Update on Molecular Diagnostic Testing of Human Imprinting Disorders

von Grafodatskaya, Daria, Choufani, Sanaa, Basran, Raveen, Weksberg, Rosanna
Veröffentlicht in J Pediatr Genet (2017)

Schizophrenia and Genetics: New Insights

von Bassett, Anne S., Chow, Eva W., Weksberg, Rosanna, Brzustowicz, Linda
Veröffentlicht 2002

Phenotype of Adults With the 22q11 Deletion Syndrome: A Review

von Cohen, Eyal, Chow, Eva W. C., Weksberg, Rosanna, Bassett, Anne S.
Veröffentlicht 1999

Don’t brush off buccal data heterogeneity

von Turinsky, Andrei L., Butcher, Darci T., Choufani, Sanaa, Weksberg, Rosanna, Brudno, Michael
Veröffentlicht in Epigenetics (2019)

Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith–Wiedemann syndrome and Silver–Russell syndrome

von Nativio, Raffaella, Sparago, Angela, Ito, Yoko, Weksberg, Rosanna, Riccio, Andrea, Murrell, Adele
Veröffentlicht 2011

Comparison of genome-wide and gene-specific DNA methylation between ART and naturally conceived pregnancies

von Melamed, Nir, Choufani, Sanaa, Wilkins-Haug, Louise E, Koren, Gideon, Weksberg, Rosanna
Veröffentlicht in Epigenetics (2015)

Cell specific patterns of methylation in the human placenta

von Grigoriu, Ariadna, Ferreira, Jose Carlos, Choufani, Sanaa, Baczyk, Dora, Kingdom, John, Weksberg, Rosanna
Veröffentlicht 2011

Catechol-O-methyl Transferase and Expression of Schizophrenia in 73 Adults with 22q11 Deletion Syndrome

von Bassett, Anne S., Caluseriu, Oana, Weksberg, Rosanna, Young, Donald A., Chow, Eva W.C.
Veröffentlicht 2007

Cross-Reactive DNA Microarray Probes Lead to False Discovery of Autosomal Sex-Associated DNA Methylation

von Chen, Yi-an, Choufani, Sanaa, Grafodatskaya, Daria, Butcher, Darci T., Ferreira, Jose C., Weksberg, Rosanna
Veröffentlicht 2012

Paternal Uniparental Disomy of the Entire Chromosome 20 in a Child with Beckwith-Wiedemann Syndrome

von Choufani, Sanaa, Ko, Jung Min, Lou, Youliang, Shuman, Cheryl, Fishman, Leona, Weksberg, Rosanna
Veröffentlicht in Genes (Basel) (2021)

A method for accurate detection of genomic microdeletions using real-time quantitative PCR

von Weksberg, Rosanna, Hughes, Simon, Moldovan, Laura, Bassett, Anne S, Chow, Eva WC, Squire, Jeremy A
Veröffentlicht 2005

22q11 Deletion Syndrome in Adults With Schizophrenia

von Bassett, Anne S., Hodgkinson, Kathy, Chow, Eva W.C., Correia, Susana, Scutt, Laura E., Weksberg, Rosanna
Veröffentlicht 1998

The Schizophrenia Phenotype in 22q11 Deletion Syndrome

von Bassett, Anne S., Chow, Eva W.C., AbdelMalik, Philip, Gheorghiu, Mirona, Husted, Janice, Weksberg, Rosanna
Veröffentlicht 2003

22q11.2 Deletion Syndrome: Attitudes towards Disclosing the Risk of Psychiatric Illness

von Martin, Nicole, Mikhaelian, Marina, Cytrynbaum, Cheryl, Shuman, Cheryl, Chitayat, David A., Weksberg, Rosanna, Bassett, Anne S.
Veröffentlicht 2012

Decreased Elastin Deposition and High Proliferation of Fibroblasts from Costello Syndrome Are Related to Functional Deficiency in the 67-kD Elastin-Binding Protein

von Hinek, Aleksander, Smith, Adam C., Cutiongco, Eva Maria, Callahan, John W., Gripp, Karen W., Weksberg, Rosanna
Veröffentlicht 2000

Sonographic Assessment of Renal Growth in Patients with Beckwith-Wiedemann Syndrome: The Beckwith-Wiedemann Syndrome Renal Nomogram

von Ortiz-Neira, Clara L, Traubici, Jeffrey, Alan, Daneman, Moineddin, Rahim, Shuman, Cheryl, Weksberg, Rosanna, Epelman, Monica
Veröffentlicht 2009