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Publications by Jenny Welander
Frequent EPAS1/HIF2 Exons 9 and 12 Mutations in Non-Familial Pheochromocytoma
Endocrine-Related Cancer
Cancer Research
Endocrinology
Oncology
Metabolism
Diabetes
Genetics and Clinical Characteristics of Hereditary Pheochromocytomas and Paragangliomas
Endocrine-Related Cancer
Cancer Research
Endocrinology
Oncology
Metabolism
Diabetes
Related publications
Mutational Profile and Genotype/Phenotype Correlation of Non-Familial Pheochromocytoma and Paraganglioma
Oncotarget
Oncology
Germ-Line Mutations in Nonsyndromic Pheochromocytoma
New England Journal of Medicine
Medicine
Somatic NF1 Inactivation Is a Frequent Event in Sporadic Pheochromocytoma
Human Molecular Genetics
Medicine
Genetics
Molecular Biology
Germline Mutations in TMEM127 Confer Susceptibility to Pheochromocytoma
Nature Genetics
Genetics
Absence of the BRCA1 Del (Exons 9–12) Mutation in Breast/Ovarian Cancer Families Outside of Mexican Hispanics
Breast Cancer Research and Treatment
Cancer Research
Oncology
Short Tandem Repeats in Human Exons: A Target for Disease Mutations
BMC Genomics
Biotechnology
Genetics
Familial Catecholamine-Secreting Tumors - Three Distinct Families With Hereditary Pheochromocytoma
PCNT Point Mutations and Familial Intracranial Aneurysms
Neurology
Neurology
GCM2 -Activating Mutations in Familial Isolated Hyperparathyroidism
American Journal of Human Genetics
Genetics
