M. Raygada

发表

Congenital generalized lipodystrophy: profile of the disease and gender differences in two siblings

O. Rennert, M. Raygada, 2004, Clinical genetics.

Proceedings of the Comprehensive Oncology Network Evaluating Rare CNS Tumors (NCI-CONNECT) Adult Medulloblastoma Workshop.

K. Aldape, M. Gilbert, G. Rao, 2020, Neuro-oncology advances.

Clinical, Diagnostic, and Treatment Characteristics of SDHA-Related Metastatic Pheochromocytoma and Paraganglioma

A. Chen, C. Stratakis, E. Kebebew, 2019, Front. Oncol..

Glucagon-like peptide-1 affects gene transcription and messenger ribonucleic acid stability of components of the insulin secretory system in RIN 1046-38 cells.

J. Egan, Yihong Wang, C. Montrose‐Rafizadeh, 1995, Endocrinology.

Case report of adrenocortical carcinoma associated with double germline mutations in MSH2 and RET

Karlyne M. Reilly, M. Raffeld, K. Reilly, 2021, American journal of medical genetics. Part A.

GIP regulates glucose transporters, hexokinases, and glucose-induced insulin secretion in RIN 1046-38 cells

J. Egan, Yihong Wang, L. Adams, 1996, Molecular and Cellular Endocrinology.

A maternal diet high in n - 6 polyunsaturated fats alters mammary gland development, puberty onset, and breast cancer risk among female rat offspring.

R Clarke, R. Clarke, L. Hilakivi-Clarke, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Early Life Affects the Risk of Developing Breast Cancer

R. Clarke, L. Hilakivi-Clarke, M. Lippman, 1995, Annals of the New York Academy of Sciences.

Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice.

C. Stratakis, C. Eng, M. Lodish, 2015, The Journal of clinical endocrinology and metabolism.

Clinical presentations, biochemical phenotypes, and genotype-phenotype correlations in patients with succinate dehydrogenase subunit B-associated pheochromocytomas and paragangliomas.

K. Pacak, H. Timmers, J. Lenders, 2007, The Journal of clinical endocrinology and metabolism.

Effects of nicotine on body weight and plasma insulin in female and male rats.

N. Grunberg, Mazen I. Saah, M. Raygada, 1994, Life sciences.

Juvenile xanthogranuloma in a child with previously unsuspected neurofibromatosis type 1 and juvenile myelomonocytic leukemia

C. Stratakis, J. Toretsky, D. Arthur, 2010, Pediatric blood & cancer.

Metastatic pheochromocytoma/paraganglioma related to primary tumor development in childhood or adolescence: significant link to SDHB mutations.

T. Fojo, C. Stratakis, E. Kebebew, 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Germline PRKACA amplification causes variable phenotypes that may depend on the extent of the genomic defect: molecular mechanisms and clinical presentations.

J. Lupski, G. Braunstein, F. Faucz, 2015, European journal of endocrinology.

The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes

V. Bours, C. Stratakis, A. Horvath, 2010, Clinical genetics.

Effect of stress on hypothalamic insulin in rats

Y. Shaham, N. Grunberg, G. Kant, 1992, Brain Research Bulletin.

Counseling patients with succinate dehydrogenase subunit defects: genetics, preventive guidelines, and dealing with uncertainty

C. Stratakis, K. Pacak, Kathryn S. King, 2014, Journal of pediatric endocrinology & metabolism : JPEM.

Rieger's Anomaly and Other Ocular Abnormalities in Association with Osteogenesis Imperfecta and a COL1A1 Mutation

C. Stratakis, O. Rennert, B. U. Nwosu, 2005, Ophthalmic genetics.

Barakat syndrome revisited

O. Rennert, M. Raygada, A. Barakat, 2018, American journal of medical genetics. Part A.

Consumption of a high-fat diet alters estrogen receptor content, protein kinase C activity, and mammary gland morphology in virgin and pregnant mice and female offspring.

L. Hilakivi-Clarke, A. Stoica, M. B. Martin, 1998, Cancer research.

Genetic Conditions Associated with Congenital Adrenocortical Insufficiency or Glucocorticoid and/or Mineralocorticoid Resistance

C. Stratakis, M. Raygada, 2016 .

Serum Estradiol Levels and Ethanol-Induced Aggression

L. Hilakivi-Clarke, E. Cho, M. Raygada, 1997, Pharmacology Biochemistry and Behavior.

Early Postnatal Treatment With Transforming Growth Factor α Does Not Alter Nonreproductive Behavior

L. Hilakivi-Clarke, E. Cho, M. Raygada, 1997, Physiology & Behavior.

Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates

C. Stratakis, S. Kurtoğlu, C. Lyssikatos, 2016, Journal of clinical research in pediatric endocrinology.

Idiopathic Autism: Cellular and Molecular Phenotypes in Pluripotent Stem Cell-Derived Neurons

D. Hoffman, E. Campanac, A. Thurm, 2016, Molecular Neurobiology.

Genomics of autism spectrum disorders

O. Rennert, M. Raygada, P. Grant, 2020 .

Case report: Oligodendroglioma, IDH-mutant and 1p/19q-codeleted, associated with a germline mutation in PMS2

M. Gilbert, M. Raffeld, J. Heiss, 2022, Frontiers in Oncology.

Case Report of an Adrenocortical Carcinoma Associated With Germline CHEK2 Mutation

C. Xie, Jeremy L. Davis, J. Del Rivero, 2018, Journal of the Endocrine Society.

NEWLY DIAGNOSED CARNEY COMPLEX IN 3 YOUNG ADULTS WITH PRIMARY ADRENAL CUSHING SYNDROME – A CASE SERIES AND REVIEW OF THE LITERATURE

F. Faucz, C. Stratakis, A. Tirosh, 2017 .

High maternal intake of polyunsaturated fatty acids during pregnancy in mice alters offsprings' aggressive behavior, immobility in the swim test, locomotor activity and brain protein kinase C activity.

L. Hilakivi-Clarke, E. Cho, M. Raygada, 1998, The Journal of nutrition.

Nutritional Neurosciences High Maternal Intake of Polyunsaturated Fatty Acids During Pregnancy in Mice Alters Offsprings ’ Aggressive Behavior , Immobility in the Swim Test , Locomotor Activity and Brain Protein Kinase C Activity 1 , 2 , 3

L. Hilakivi-Clarke, E. Cho, M. Raygada, 1998 .

Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations

R. Hennekam, L. Biesecker, J. Graham, 2010, Human mutation.

Molecular Subtypes of KIT/PDGFRA Wild-Type Gastrointestinal Stromal Tumors: A Report From the National Institutes of Health Gastrointestinal Stromal Tumor Clinic.

P. Meltzer, J. Schiffman, C. Stratakis, 2016, JAMA oncology.

Alterations in mammary gland development following neonatal exposure to estradiol, transforming growth factor α, and estrogen receptor antagonist ICI 182,780

L. Hilakivi-Clarke, N. Kenney, E. Cho, 1997, Journal of cellular physiology.

The Effects of Cocaine and Stress on Lymphocyte Proliferation in Rats

M. Raygada, L. Cohen, 1993 .

Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations

C. Antonescu, M. O'sullivan, J. Fletcher, 2010, Proceedings of the National Academy of Sciences.

A novel AVPR2 splice site mutation leads to partial X-linked nephrogenic diabetes insipidus in two brothers

F. Faucz, C. Tifft, W. Gahl, 2016, European Journal of Pediatrics.

ZNF764 haploinsufficiency may explain partial glucocorticoid, androgen, and thyroid hormone resistance associated with 16p11.2 microdeletion.

C. Stratakis, T. Kino, M. Pavlatou, 2012, The Journal of clinical endocrinology and metabolism.

Carney triad can be (rarely) associated with germline succinate dehydrogenase defects

F. Faucz, C. Stratakis, L. Helman, 2015, European Journal of Human Genetics.

A. Fojo, K. Pacak, R. Wesley, 2017, Journal of Cancer Research and Clinical Oncology.

Adrenocortical carcinoma masquerading as pheochromocytoma: a histopathologic dilemma

M. Merino, K. Reilly, B. Widemann, 2019, Endocrinology, diabetes & metabolism case reports.

Germline AIP, MEN1, PRKAR1A, CDKN1B (p27Kip1) and CDKN2C (p18INK4c) gene mutations in a large cohort of pediatric patients with pituitary adenomas occurring in isolation or with associated syndromic features

V. Bours, C. Stratakis, A. Horvath, 2008 .

Update on Targeted Therapy in Medullary Thyroid Cancer

Christian Okafor, J. Glod, J. Del Rivero, 2021, Frontiers in Endocrinology.

Prepubertal exposure to zearalenone or genistein reduces mammary tumorigenesis

R. Clarke, T. Skaar, L. Hilakivi-Clarke, 1999, British Journal of Cancer.

Maternal exposure to genistein during pregnancy increases carcinogen-induced mammary tumorigenesis in female rat offspring.

R. Clarke, L. Hilakivi-Clarke, E. Cho, 1999, Oncology reports.

Integrative gene network analysis provides novel regulatory relationships, genetic contributions and susceptible targets in autism spectrum disorders.

Owen M Rennert, Tin-Lap Lee, O. Rennert, 2012, Gene.

EXTENSIVE CLINICAL EXPERIENCE Clinical Presentations, Biochemical Phenotypes, and Genotype-Phenotype Correlations in Patients with Succinate Dehydrogenase Subunit B-Associated Pheochromocytomas and Paragangliomas

K. Pacak, H. Timmers, J. Lenders, 2007 .

Breast cancer risk in rats fed a diet high in n-6 polyunsaturated fatty acids during pregnancy.

R. Clarke, L. Hilakivi-Clarke, M. Lippman, 1996, Journal of the National Cancer Institute.

Effects of Nicotine on Insulin: Actions and Implications

N. Grunberg, M. Raygada, 1991 .

A woman with spontaneous premature ovarian failure gives birth to a child with fragile X syndrome.

L. Nelson, M. Raygada, V. Vanderhoof, 2005, Fertility and sterility.

Association of brain-derived neurotrophic factor (BDNF) haploinsufficiency with lower adaptive behaviour and reduced cognitive functioning in WAGR/11p13 deletion syndrome

K. Martinowich, J. Tsao, J. Butman, 2013, Cortex.

The NIH pediatric/young adult chordoma clinic and natural history study: Making advances in a very rare tumor

Deric M. Park, Karlyne M. Reilly, P. Gardner, 2023, Pediatric blood & cancer.

NCI intramural program approach to rare tumors: Natural history study of rare solid tumors in children and adults: A longitudinal, comprehensive data and biospecimen collection protocol

Karlyne M. Reilly, K. Reilly, B. Widemann, 2023, Pediatric blood & cancer.

Penetrance and clinical consequences of a gross SDHB deletion in a large family

A. Vénisse, K. Pacak, H. Timmers, 2009, Clinical genetics.