Alison Brown

发表

The NEI/NCBI dbGAP database: Genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration

Ivana K. Kim, Josephine Hoh, Nancy Huynh, 2008, BMC Medical Genetics.

Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes.

E. Silverman, F. Speizer, L. Palmer, 2002, Human molecular genetics.

Single-nucleotide polymorphisms in the interleukin-10 gene: differences in frequencies, linkage disequilibrium patterns, and haplotypes in three United States ethnic groups.

E. Silverman, L. Palmer, R. Lazarus, 2002, Genomics.

A novel, single nucleotide polymorphism-based assay to detect 22q11 deletions.

R. Kucherlapati, R. Shprintzen, B. Morrow, 2007, Genetic testing.

The IL12B gene is associated with asthma.

E. Silverman, A. Randolph, C. Lange, 2004, American journal of human genetics.

Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.

Andrew D Bolton, Danielle K. Manning, R. Kucherlapati, 2006, Genome research.

A genome-wide scan in families with maturity-onset diabetes of the young: evidence for further genetic heterogeneity.

T. Hansen, O. Pedersen, C. Lindgren, 2003, Diabetes.

Genomewide linkage analysis of quantitative spirometric phenotypes in severe early-onset chronic obstructive pulmonary disease.

Edwin K Silverman, Scott T Weiss, D C Rao, 2002, American journal of human genetics.

Integrating de novo and inherited variants in over 42,607 autism cases identifies mutations in new moderate risk genes

William T. Harvey, Richard A Marini, Simon X. Xu, 2021, medRxiv.

The preoptic area/anterior hypothalamus of different strains of mice: sex differences and development.

S. Tobet, S. Mani, Alison Brown, 1999, Brain research. Developmental brain research.

Amplification of EGFR T790M causes resistance to an irreversible EGFR inhibitor

P. Jänne, J. Engelman, J. Christensen, 2010, Oncogene.