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A Stephan

Showing results (201-210 of 223) with videos related to

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Cancer Research|March 9, 2005
An expression signature classifies chemotherapy-resistant pediatric osteosarcomaMichelle B Mintz, Rebecca Sowers, Kevin M Brown, et al.
Molecular Psychiatry|February 28, 2008
Genome-wide linkage analysis of ADHD using high-density SNP arrays: novel loci at 5q13.1 and 14q12M Romanos, C Freitag, C Jacob, et al.
Human Genetics|May 21, 2005
A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX regionAgnes B Baffoe-Bonnie, Jeffrey R Smith, Dietrich A Stephan, et al.
Genomics|March 10, 2000
A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) regionJ D Carpten, I Makalowska, C M Robbins, et al.
Science (New York, N.Y.)|October 21, 2006
Common Kibra alleles are associated with human memory performanceAndreas Papassotiropoulos, Dietrich A Stephan, Matthew J Huentelman, et al.
The Journal of Clinical Psychiatry|May 4, 2007
A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's diseaseKeith D Coon, Amanda J Myers, David W Craig, et al.
Neuro-Degenerative Diseases|November 3, 2007
Sorl1 as an Alzheimer's disease predisposition gene?Jennifer A Webster, Amanda J Myers, John V Pearson, et al.
Human Genetics|April 6, 2002
A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genesEster Rozenblum, Pia Vahteristo, Therese Sandberg, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|January 1, 2021
Relevance of body mass index as a predictor of systemic therapy outcomes in metastatic melanoma: analysis of the MelBase French cohort data<sup>☆</sup>Y Di Filippo, S Dalle, L Mortier, et al.
American Journal of Human Genetics|December 13, 2006
Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studiesJohn V Pearson, Matthew J Huentelman, Rebecca F Halperin, et al.
Pageof 23

Showing results (201-210 of 223) with videos related to

Sort By:
Pageof 23
Cancer Research|March 9, 2005
An expression signature classifies chemotherapy-resistant pediatric osteosarcomaMichelle B Mintz, Rebecca Sowers, Kevin M Brown, et al.
Molecular Psychiatry|February 28, 2008
Genome-wide linkage analysis of ADHD using high-density SNP arrays: novel loci at 5q13.1 and 14q12M Romanos, C Freitag, C Jacob, et al.
Human Genetics|May 21, 2005
A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX regionAgnes B Baffoe-Bonnie, Jeffrey R Smith, Dietrich A Stephan, et al.
Genomics|March 10, 2000
A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) regionJ D Carpten, I Makalowska, C M Robbins, et al.
Science (New York, N.Y.)|October 21, 2006
Common Kibra alleles are associated with human memory performanceAndreas Papassotiropoulos, Dietrich A Stephan, Matthew J Huentelman, et al.
The Journal of Clinical Psychiatry|May 4, 2007
A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's diseaseKeith D Coon, Amanda J Myers, David W Craig, et al.
Neuro-Degenerative Diseases|November 3, 2007
Sorl1 as an Alzheimer's disease predisposition gene?Jennifer A Webster, Amanda J Myers, John V Pearson, et al.
Human Genetics|April 6, 2002
A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genesEster Rozenblum, Pia Vahteristo, Therese Sandberg, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|January 1, 2021
Relevance of body mass index as a predictor of systemic therapy outcomes in metastatic melanoma: analysis of the MelBase French cohort data<sup>☆</sup>Y Di Filippo, S Dalle, L Mortier, et al.
American Journal of Human Genetics|December 13, 2006
Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studiesJohn V Pearson, Matthew J Huentelman, Rebecca F Halperin, et al.
Pageof 23