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A Nickel Complex Containing a Pyramidalized, Ambiphilic Pincer Germylene Ligand

Chemistry : a European journal, 2019-10, Vol.25 (59), p.13491-13495

2019

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Massive parallel sequencing uncovers actionable FGFR2–PPHLN1 fusion and ARAF mutations in intrahepatic cholangiocarcinoma

Nature communications, 2015-01, Vol.6 (1), Article 6087

2015

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Insights into beta cell regeneration for diabetes via integration of molecular landscapes in human insulinomas

Nature communications, 2017-10, Vol.8 (1), p.767-15, Article 767

2017

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Novel MEK1 mutation identified by mutational analysis of epidermal growth factor receptor signaling pathway genes in lung adenocarcinoma

Cancer research (Chicago, Ill.), 2008-07, Vol.68 (14), p.5524-5528

2008

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Analytical validation of whole exome and whole genome sequencing for clinical applications

BMC medical genomics, 2014-04, Vol.7 (1), p.20-20, Article 20

2014

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Tamoxifen Metabolite Isomer Separation and Quantification by Liquid Chromatography−Tandem Mass Spectrometry

Analytical chemistry (Washington), 2010-12, Vol.82 (24), p.10186-10193

2010

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Integrated genomic analysis implicates haploinsufficiency of multiple chromosome 5q31.2 genes in de novo myelodysplastic syndromes pathogenesis

PloS one, 2009-02, Vol.4 (2), p.e4583

2009

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Mutational analysis of EGFR and related signaling pathway genes in lung adenocarcinomas identifies a novel somatic kinase domain mutation in FGFR4

PloS one, 2007-05, Vol.2 (5), p.e426-e426

2007

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Massive parallel sequencing uncovers actionable FGFR2–PPHLN1 fusion and ARAF mutations in intrahepatic cholangiocarcinoma

Nature communications, 2015-01, Vol.6 (1), p.6087-6087

2015

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Effects of Tai Chi Chuan on cognition of elderly women with mild cognitive impairment

Einstein (São Paulo, Brazil), 2010-03, Vol.8 (1), p.40-45

2010

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Frequency of the cholesteryl ester storage disease common LIPA E8SJM mutation (c.894G>A) in various racial and ethnic groups

Hepatology (Baltimore, Md.), 2013-09, Vol.58 (3), p.958-965

2013

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Drosophila as a tool for personalized medicine: a primer

Personalized medicine, 2010-11, Vol.7 (6), p.621-632

2010

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C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy

Nature genetics, 2007-09, Vol.39 (9), p.1068-1070

2007

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Control of CNS midline transcription by asymmetric E-box-like elements: similarity to xenobiotic responsive regulation

Development (Cambridge), 1994-12, Vol.120 (12), p.3563-3569

1994

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Characterizing spontaneously reported cognitive complaints: the development and reliability of a classification instrument

International psychogeriatrics, 2013-01, Vol.25 (1), p.157-166

2013

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MG-134 Validation of a customizable next generation sequencing panel for ear and eye diseases

Journal of medical genetics, 2015-11, Vol.52 (Suppl 2), p.A12-A13

2015

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PolyScan: an automatic indel and SNP detection approach to the analysis of human resequencing data

Genome Research, 2007-05, Vol.17 (5), p.659-666

2007

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Identification of somatic JAK1 mutations in patients with acute myeloid leukemia

Blood, 2008-05, Vol.111 (9), p.4809-4812

2008

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The Roberts syndrome/SC phocomelia spectrum—A case report of an adult with review of the literature

American journal of medical genetics. Part A, 2010-02, Vol.152A (2), p.472-478

2010

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Absence of Mutations in the Epidermal Growth Factor Receptor (EGFR) Kinase Domain in Patients with Mesothelioma

Journal of thoracic oncology, 2009-04, Vol.4 (4), p.559-559

2009

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A TATA-like sequence located downstream of the transcription initiation site is required for expression of an RNA polymerase II transcribed gene

Genes & development, 1990-09, Vol.4 (9), p.1611-1622

1990

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Identification of a novel RASD1 somatic mutation in a USP8 -mutated corticotroph adenoma

Cold Spring Harbor molecular case studies, 2017-05, Vol.3 (3), p.a001602-a001602

2017

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A Nickel Complex Containing a Pyramidalized, Ambiphilic Pincer Germylene Ligand

Massive parallel sequencing uncovers actionable FGFR2–PPHLN1 fusion and ARAF mutations in intrahepatic cholangiocarcinoma

Insights into beta cell regeneration for diabetes via integration of molecular landscapes in human insulinomas

Novel MEK1 mutation identified by mutational analysis of epidermal growth factor receptor signaling pathway genes in lung adenocarcinoma

Analytical validation of whole exome and whole genome sequencing for clinical applications

Tamoxifen Metabolite Isomer Separation and Quantification by Liquid Chromatography−Tandem Mass Spectrometry

Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropenia

Integrated genomic analysis implicates haploinsufficiency of multiple chromosome 5q31.2 genes in de novo myelodysplastic syndromes pathogenesis

Mutational analysis of EGFR and related signaling pathway genes in lung adenocarcinomas identifies a novel somatic kinase domain mutation in FGFR4

Massive parallel sequencing uncovers actionable FGFR2–PPHLN1 fusion and ARAF mutations in intrahepatic cholangiocarcinoma

Effects of Tai Chi Chuan on cognition of elderly women with mild cognitive impairment

Frequency of the cholesteryl ester storage disease common LIPA E8SJM mutation (c.894G>A) in various racial and ethnic groups

Drosophila as a tool for personalized medicine: a primer

C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy

Somatic mutations and germline sequence variants in the expressed tyrosine kinase genes of patients with de novo acute myeloid leukemia

Control of CNS midline transcription by asymmetric E-box-like elements: similarity to xenobiotic responsive regulation

Development and clinical application of an integrative genomic approach to personalized cancer therapy

Characterizing spontaneously reported cognitive complaints: the development and reliability of a classification instrument

MG-134 Validation of a customizable next generation sequencing panel for ear and eye diseases

PolyScan: an automatic indel and SNP detection approach to the analysis of human resequencing data

Identification of somatic JAK1 mutations in patients with acute myeloid leukemia

The Roberts syndrome/SC phocomelia spectrum—A case report of an adult with review of the literature

Absence of Mutations in the Epidermal Growth Factor Receptor (EGFR) Kinase Domain in Patients with Mesothelioma

A TATA-like sequence located downstream of the transcription initiation site is required for expression of an RNA polymerase II transcribed gene

Identification of a novel RASD1 somatic mutation in a USP8 -mutated corticotroph adenoma

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