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Use of pairwise marker combination and recursive partitioning in a pharmacogenetic genome-wide scan

The pharmacogenomics journal, 2007-06, Vol.7 (3), p.180-189

2007

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Cancer nanomedicine: progress, challenges and opportunities

Nature reviews. Cancer, 2017-01, Vol.17 (1), p.20-37

2017

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Subtype and pathway specific responses to anticancer compounds in breast cancer

Proceedings of the National Academy of Sciences - PNAS, 2012-02, Vol.109 (8), p.2724-2729

2012

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High-resolution analysis of DNA copy number using oligonucleotide microarrays

Genome research, 2004-02, Vol.14 (2), p.287-295

2004

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Current and future diagnostic and treatment strategies for patients with invasive lobular breast cancer

Annals of oncology, 2022-08, Vol.33 (8), p.769-785

2022

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Occlusion of the Celiac Artery during Endovascular Thoracoabdominal Aortic Aneurysm Repair Is associated with Increased Perioperative Morbidity and Mortality

Annals of vascular surgery, 2020-07, Vol.66, p.200-211

2020

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Etiologies of Acute Undifferentiated Febrile Illnesses in and near Iquitos from 1993 to 1999 in the Amazon River Basin of Peru

The American journal of tropical medicine and hygiene, 2022-11, Vol.107 (5), p.1114-1128

2022

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Exercise Pulmonary Hypertension Predicts Clinical Outcomes in Patients With Dyspnea on Effort

Journal of the American College of Cardiology, 2020-01, Vol.75 (1), p.17-26

2020

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Antitumor activity of an allosteric inhibitor of centromere-associated protein-E

Proceedings of the National Academy of Sciences - PNAS, 2010-03, Vol.107 (13), p.5839-5844

2010

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Contemporary rates of inferior vena cava filter thrombosis and risk factors

Journal of vascular surgery. Venous and lymphatic disorders (New York, NY), 2022-03, Vol.10 (2), p.313-324

2022

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Similarity of the phenotypic patterns associated with BRAF and KRAS mutations in colorectal neoplasia

Cancer research (Chicago, Ill.), 2002-11, Vol.62 (22), p.6451-6455

2002

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Mutations of the BRAF gene in human cancer

Nature (London), 2002-06, Vol.417 (6892), p.949-954

2002

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CHA 2 DS 2 -VASc and has-BLED scores do not accurately stratify risk for stroke or bleed in fall victims with atrial fibrillation

The American journal of emergency medicine, 2022-01, Vol.51, p.119

2022

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Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution

Genome Research, 2007-09, Vol.17 (9), p.1296-1303

2007

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Mutations in FRMD7 , a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Nature genetics, 2006-11, Vol.38 (11), p.1242-1244

2006

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Integrated analysis of breast cancer cell lines reveals unique signaling pathways

Genome biology, 2009-03, Vol.10 (3), p.R31-R31

2009

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A Survey of Homozygous Deletions in Human Cancer Genomes

Proceedings of the National Academy of Sciences - PNAS, 2005-03, Vol.102 (12), p.4542-4547

2005

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Whole genome DNA copy number changes identified by high density oligonucleotide arrays

Human genomics, 2004-05, Vol.1 (4), p.287-299

2004

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BRCA2 mutations in primary breast and ovarian cancers

Nature genetics, 1996-06, Vol.13 (2), p.238-240

1996

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Genome co-amplification upregulates a mitotic gene network activity that predicts outcome and response to mitotic protein inhibitors in breast cancer

Breast cancer research : BCR, 2016-07, Vol.18 (1), p.70, Article 70

2016

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Periprosthetic Joint Infection After Total Knee Arthroplasty With or Without Antibiotic Bone Cement

JAMA network open, 2024-05, Vol.7 (5), p.e2412898-e2412898

2024

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Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13

American journal of human genetics, 1997-07, Vol.61 (1), p.120-128

1997

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AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes

Bioinformatics, 2007-07, Vol.23 (13), p.1689-1691

2007

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Evidence for direct interaction between actin and the cystic fibrosis transmembrane conductance regulator

European biophysics journal, 2002-02, Vol.30 (8), p.617-624

2002

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Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13

Oncogene, 1995-04, Vol.10 (8), p.1673-1675

1995

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Use of pairwise marker combination and recursive partitioning in a pharmacogenetic genome-wide scan

Cancer nanomedicine: progress, challenges and opportunities

Subtype and pathway specific responses to anticancer compounds in breast cancer

High-resolution analysis of DNA copy number using oligonucleotide microarrays

Current and future diagnostic and treatment strategies for patients with invasive lobular breast cancer

Occlusion of the Celiac Artery during Endovascular Thoracoabdominal Aortic Aneurysm Repair Is associated with Increased Perioperative Morbidity and Mortality

Etiologies of Acute Undifferentiated Febrile Illnesses in and near Iquitos from 1993 to 1999 in the Amazon River Basin of Peru

Exercise Pulmonary Hypertension Predicts Clinical Outcomes in Patients With Dyspnea on Effort

Antitumor activity of an allosteric inhibitor of centromere-associated protein-E

Contemporary rates of inferior vena cava filter thrombosis and risk factors

Similarity of the phenotypic patterns associated with BRAF and KRAS mutations in colorectal neoplasia

Mutations of the BRAF gene in human cancer

CHA 2 DS 2 -VASc and has-BLED scores do not accurately stratify risk for stroke or bleed in fall victims with atrial fibrillation

Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution

Mutations in FRMD7 , a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Integrated analysis of breast cancer cell lines reveals unique signaling pathways

A Survey of Homozygous Deletions in Human Cancer Genomes

Whole genome DNA copy number changes identified by high density oligonucleotide arrays

BRCA2 mutations in primary breast and ovarian cancers

Genome co-amplification upregulates a mitotic gene network activity that predicts outcome and response to mitotic protein inhibitors in breast cancer

Periprosthetic Joint Infection After Total Knee Arthroplasty With or Without Antibiotic Bone Cement

Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13

AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes

Evidence for direct interaction between actin and the cystic fibrosis transmembrane conductance regulator

Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13

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