1,115 results on '"Goldstein, Alisa M."'
Search Results
102. Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations
103. Index-based dietary patterns and risk of incident hepatocellular carcinoma and mortality from chronic liver disease in a prospective study
104. Genetic variants in fas signaling pathway genes and risk of gastric cancer
105. A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma
106. Rare Germline Variants in Chordoma-Related Genes and Chordoma Susceptibility
107. Mutational signatures in esophageal squamous cell carcinoma from eight countries of varying incidence
108. Integrative molecular characterisation of gallbladder cancer reveals micro-environment-associated subtypes
109. Clinical findings in families with chordoma with and without T gene duplications and in patients with sporadic chordoma reported to the Surveillance, Epidemiology, and End Results program
110. The Impact of Longitudinal Surveillance on Tumor Thickness for Melanoma-Prone Families with and without Pathogenic Germline Variants of CDKN2A and CDK4
111. Additional file 8 of Integrated analysis of genome-wide miRNAs and targeted gene expression in esophageal squamous cell carcinoma (ESCC) and relation to prognosis
112. Integrative molecular characterization of gallbladder cancer reveals microenvironment-associated subtypes
113. A mutation hotspot at the p14ARF splice site
114. Histologic features of melanoma associated with CDKN2A genotype
115. Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study
116. Sebaceous Carcinoma Epidemiology and Genetics: Emerging Concepts and Clinical Implications for Screening, Prevention, and Treatment
117. Evaluation of BRCA2 in the genetic susceptibility of familial esophageal cancer
118. Sebaceous Carcinoma Incidence and Survival Among Solid Organ Transplant Recipients in the United States, 1987-2017
119. Germline splicing mutations of CDKN2A predispose to melanoma
120. CDKN2A point mutations D153spl(c.457G>T) and IVS2+1G>T result in aberrant splice products affecting both p16INK4a and p14ARF
121. Melanoma etiology: where are we?
122. Allelic loss on chromosome 13q14 and mutation in deleted in cancer 1 gene in esophageal squamous cell carcinoma
123. Genetic variants in DNA repair pathway genes and risk of esophageal squamous cell carcinoma and gastric adenocarcinoma in a Chinese population
124. Genetic variants in sex hormone metabolic pathway genes and risk of esophageal squamous cell carcinoma
125. Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants
126. Localization of a novel melanoma susceptibility locus to 1p22
127. Lack of germline CDK6 mutations in familial melanoma
128. Genetic variants in DNA repair genes and the risk of cutaneous malignant melanoma in melanoma-prone families with/without CDKN2A mutations
129. Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies
130. Duplication of CXC chemokine genes on chromosome 4q13 in a melanoma-prone family
131. InterSCOPE Study: Associations Between Esophageal Squamous Cell Carcinoma and Human Papillomavirus Serological Markers
132. High-risk pregnancy and neonatal complications in the DNA repair and transcription disorder trichothiodystrophy: report of 27 affected pregnancies
133. Clinical features distinguish childhood chordoma associated with tuberous sclerosis complex (TSC) from chordoma in the general paediatric population
134. Assessment of Human Papillomavirus in Lung Tumor Tissue
135. Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair
136. Histologic features of melanoma associated with germline mutations of CDKN2A, CDK4, and POT1 in melanoma-prone families from the United States, Italy, and Spain
137. A Systematic Literature Review of Whole Exome and Genome Sequencing Population Studies of Genetic Susceptibility to Cancer
138. Integrated analysis of genome-wide miRNAs and targeted gene expression in esophageal squamous cell carcinoma (ESCC) and relation to prognosis
139. Low Epstein–Barr Virus Prevalence in Cardia Gastric Cancer Among a High-Incidence Chinese Population
140. Ambient Ultraviolet Radiation and Sebaceous Carcinoma Incidence in the United States, 2000–2016
141. Body mass index and height and risk of cutaneous melanoma: Mendelian randomization analyses
142. Dietary quercetin, quercetin-gene interaction, metabolic gene expression in lung tissue and lung cancer risk
143. Increased Risk of Second Primary Cancers After a Diagnosis of Melanoma
144. Alcohol Consumption and Lung Cancer Risk in the Environment and Genetics in Lung Cancer Etiology (EAGLE) Study
145. Identification of modifier genes for cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutations
146. Meeting report: consensus from the first and second Global Workshops in Melanoma November 19-20, 2008
147. Lack of inherited mutations of PTPRD in familial melanoma and melanoma-astrocytoma syndrome
148. Family history of cancer and nonmalignant lung diseases as risk factors for lung cancer
149. Cancer patterns in nasopharyngeal carcinoma multiplex families in Taiwan
150. Acral Lentiginous Melanoma: Incidence and Survival Patterns in the United States, 1986-2005
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.