Cancer SIG Research Directory

These pages are produced by the National Society of Genetic Counselors' Cancer Special Interest Group and are for use by members of the NSGC.

Please do not link these pages to another website without permission. To add or modify a study entry, please contact Robert Pilarski at (614) 293-7774 or Robert.Pilarski@osumc.edu

Last modified on November 5, 2018.

Please use the following links to go the specific study pages in the document repository.

ADRENOCORTICAL

ID 112

International Pediatric Adrenocortical Registry (IPACTR)

BAP1

ID 139

Frequency and Clinical Phenotype of BAP1 Tumor Predisposition Syndrome

BREAST/OVARIAN CANCER, BRCA TESTING

ID 106	The DCIS and BRCA1/2 Cohort Study
ID 117	ICARE (Inherited Cancer Registry) at the Moffitt Cancer Center
ID 136	Cancer Prevention in Women With a BRCA Mutation: A Follow-Up Telephone Genetic Counselling Study
ID 138	Evaluation of Screening Management iPhone App for BRCA Mutation Carriers
ID 140	MAking GENetic Testing Accessible (MAGENTA) Psychosocial Issues

CANCER SUSCEPTIBILITY

ID 51	Cancer Risk Assessment and Genetic Screening
ID 134	Inherited Bone Marrow Failure Syndromes Study (IBMFSS)
ID 88	Prenatal Chemotherapy: Implications for Child Development
ID 141	Familial Investigations of Childhood Cancer Predisposition (SJFAMILY)

CARNEY COMPLEX, PPNADID

ID 133

Definition of the Genotype and Clinical Phenotype of Primary Pigmented Nodular Adrenocortical Diseases (PPNAD), Carney Complex, Peutz-Jeghers Syndrome, and Related Conditions

CHORDOMA

ID 40

Genetic Aspects of Chordoma

COLON CANCER

ID 33	Huntsman Cancer Institute Familial Colon Cancer Registry
ID 108	FAP Mutation-Negative Study

COWDEN SYNDROME

ID 71

Comparative Genotype/Phenotype Correlations in Cowden syndrome and Bannayan-Ruvalcaba-Riley syndrome

DNA REPAIR DEFECT SYNDROMES

ID 135

Examination of Clinical and Laboratory Abnormalities in Patients With Defective DNA Repair: Zeroderma Pigmentosum, Cockayne Syndrome, or Trichothiodystrophy

GASTRIC

ID 69

Genetic Factors in Hereditary Diffuse Gastric Cancer

HEMATOLOGIC

ID 75	Familial Multiple Myeloma
ID 99	Familial Hematological Malignancies
ID 134	Inherited Bone Marrow Failure Syndromes Study (IBMFSS)
ID 137	Identification of Genetic Factors Contributing to Lymphoid Cancers

LI FRAUMENI/LIKE

ID 124	Li-Fraumeni Syndrome
ID 143	Registry of Patients in Kindreds with Germline TP53 Mutations (Li-Fraumeni syndrome)

LUNG

ID 49	Genetic Epidemiology of Lung Cancer: Gene Identification in High-Risk Families
ID 127	Determination of Genetic Susceptibility to Lung Cancer in Families from Southern Louisiana

MELANOMA

ID 100

The Genetics of Hereditary Uveal Melanoma

OVERGROWTH SYNDROMES (Beckwith-Wiedemann, Sotos, Weaver)

ID 131

Investigation of Genetic and Environmental Factors in Individuals with Advanced or Delayed Growth with or without Developmental Delay

PANCREAS

ID 83

Pancreatic Cancer Genes Study (PAGES)

PAPILLARY THYROID AND RENAL CANCERS

ID 52

Familial Papillary Thyroid and Papillary Renal Cancers

PARAGANGLIOMA

ID 93	Genetic Analysis of Pheochromocytoma and Paraganglioma
ID 98	Genetics of Pheochromocytoma and Paraganglioma

PEDIATRIC

ID 71	Comparative Genotype/Phenotype Correlations in Cowden syndrome and Bannayan-Ruvalcaba-Riley syndrome
ID 98	Genetics of Pheochromocytoma and Paraganglioma
ID 128	Definition of molecular signatures for unilateral and bilateral Wilms tumours using genome‐wide DNA methylation arrays and whole‐exome sequencing
ID 129	Genetics of Familial Wilms Tumor
ID 131	Investigation of Genetic and Environmental Factors in Individuals with Advanced or Delayed Growth with or without Developmental Delay
ID 132	A Clinical and Genetic Investigation of Pituitary Tumors and Related Hypothalamic Disorders
ID 133	Definition of the Genotype and Clinical Phenotype of Primary Pigmented Nodular Adrenocortical Diseases (PPNAD), Carney Complex, Peutz-Jeghers Syndrome, and Related Conditions
ID 134	Inherited Bone Marrow Failure Syndromes Study (IBMFSS)
ID 135	Examination of Clinical and Laboratory Abnormalities in Patients With Defective DNA Repair: Xeroderma Pigmentosum, Cockayne Syndrome, or Trichothiodystrophy
ID 141	Familial Investigations of Childhood Cancer Predisposition (SJFAMILY)
ID 142	Familial Wilms Tumor Cohort

PITUITARY

ID 132

A Clinical and Genetic Investigation of Pituitary Tumors and Related Hypothalamic Disorders

PRIMARY PIGMENTED NODULAR ADRENOCORTICAL DISEASE

ID 133

Definition of the Genotype and Clinical Phenotype of Primary Pigmented Nodular Adrenocortical Diseases (PPNAD), Carney Complex, Peutz-Jeghers Syndrome, and Related Conditions

PROSTATE

ID 89	The Genetics of Prostate Cancer
ID 92	Identifying Prostate Cancer Genes

PSYCHOSOCIAL/COUNSELING

ID 134	Inherited Bone Marrow Failure Syndromes Study (IBMFSS)
ID 136	Cancer Prevention in Women With a BRCA Mutation: A Follow-Up Telephone Genetic Counselling Study
ID 140	MAking GENetic Testing Accessible (MAGENTA) Psychosocial Issues

RHABDOID

ID 56

Genetics of Pediatric Rhabdoid Tumors

TESTICULAR

ID 70

Familial Testicular Cancer

THYROID

ID 52	Familial Papillary Thyroid and Papillary Renal Cancers
ID 79	A Search for Genes Predisposing to Papillary Thyroid Cancer

WILMS TUMOR

ID 128	Definition of molecular signatures for unilateral and bilateral Wilms tumours using genome‐wide DNA methylation arrays and whole‐exome sequencing
ID 129	Genetics of Familial Wilms Tumor
ID 142	Familial Wilms Tumor Cohort