Julia Meade

发表

Evaluation of barriers to referral for cancer predisposition syndromes in pediatric oncology patients in the United States

R. Grubs, Rosemarie E. Venier, E. Kessler, 2022, Journal of genetic counseling.

A germline BARD1 mutation in a patient with Ewing Sarcoma: Implications for familial testing and counseling

J. Tersak, S. Ranganathan, Rosemarie E. Venier, 2019, Pediatric blood & cancer.

Familial Cerebral Cavernous Malformation Syndrome with Concomitant Fourth Ventricular Ependymoma: True Association or Mere Coincidence?

M. Mendelson, Julia Meade, G. Arnold, 2020, Cancer genetics.

B‐cell acute lymphoblastic leukemia with iAMP21 in a patient with Down syndrome due to a constitutional isodicentric chromosome 21

Julia Meade, S. Yatsenko, G. Bullock, 2021, American journal of medical genetics. Part A.

Evaluation of barriers to referral for cancer predisposition syndromes in pediatric oncology patients in the United States

R. Grubs, Rosemarie E. Venier, K. Cooper, 2020, Journal of genetic counseling.

Cutaneous Ewing Sarcoma Presenting as a Second Primary Malignancy in a Child.

J. Ozolek, Kelly M. Bailey, Julia Meade, 2022, Journal of pediatric hematology/oncology.

Constitutional POLE variants causing a phenotype reminiscent of constitutional mismatch repair deficiency

R. Pai, K. Wimmer, M. Schmuth, 2021, Human mutation.

Constitutional microsatellite instability, genotype, and phenotype correlations in Constitutional Mismatch Repair Deficiency.

L. Guerrini-Rousseau, K. Dahan, G. Borthwick, 2022, Gastroenterology.

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Y. Okada, K. Ichimura, R. Nishikawa, 2019, A Glossary of Sociolinguistics.

Multiple Primary Paragangliomas in a Pediatric Patient With von Hippel Lindau: A Diagnostic Dilemma

Julia Meade, Katelin Magnan, Qian Wang, 2024, JCEM case reports.