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Chromothriptic Cure of WHIM Syndrome

Cell, 2015-02, Vol.160 (4), p.686-699

2015

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Incidence and patterns of ALK FISH abnormalities seen in a large unselected series of lung carcinomas

Molecular cytogenetics, 2012, Vol.5 (1), p.44-44

2012

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Distinct Missense Mutations of the FGFR3 Lys650 Codon Modulate Receptor Kinase Activation and the Severity of the Skeletal Dysplasia Phenotype

American journal of human genetics, 2000-12, Vol.67 (6), p.1411-1421

2000

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Challenging cases of follicular lymphoma diagnosed by core needle biopsy incorporating proliferation index and cytogenetics

Human Pathology Reports, 2022-06, Vol.28, p.300616, Article 300616

2022

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Characteristics of myeloproliferative neoplasms in patients exposed to ionizing radiation following the Chernobyl nuclear accident

American journal of hematology, 2019-01, Vol.94 (1), p.62-73

2019

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EBV ‐positive, HHV 8‐negative large B‐cell lymphoma with an unusual germinotropic growth pattern in an immunocompetent patient

Clinical case reports, 2018-09, Vol.6 (9), p.1818-1824

2018

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EBV‐positive, HHV8‐negative large B‐cell lymphoma with an unusual germinotropic growth pattern in an immunocompetent patient

Clinical case reports, 2018-09, Vol.6 (9), p.1818-1824

2018

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Vemurafenib-resistance via de novo RBM genes mutations and chromosome 5 aberrations is overcome by combined therapy with palbociclib in thyroid carcinoma with BRAFV600E

Oncotarget, 2017-10, Vol.8 (49), p.84743-84760

2017

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WHIM Syndrome Cured by Chromothripsis

Cancer genetics, 2015-06, Vol.208 (6), p.358-359

2015

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Abstract 3093: Genomic characteristics of myeloproliferative neoplasms in patients exposed to ionizing radiation following the Chernobyl nuclear accident

Cancer research (Chicago, Ill.), 2018, Vol.78 (13_Supplement), p.3093-3093

2018

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Low expression of Abelson interactor-1 is linked to acquired drug resistance in Bcr-Abl-induced leukemia

Leukemia, 2014-11, Vol.28 (11), p.2165-2177

2014

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Marfan Syndrome Type II: There Is More to Marfan Syndrome than Fibrillin 1

Congenital heart disease, 2006-09, Vol.1 (5), p.229-232

2006

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Genomic Characteristics of Myeloproliferative Neoplasms in Patients Exposed to Ionizing Radiation following the Chernobyl Nuclear Accident

American journal of hematology, 2018-10, Vol.94 (1), p.62-73

2018

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Abstract B08: New Abelson interactor-1(Abi-1)-driven mechanism of acquired drug resistance

Clinical cancer research, 2015-02, Vol.21 (4_Supplement), p.B08-B08

2015

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Vemurafenib-resistance via de novo RBM genes mutations and chromosome 5 aberrations is overcome by combined therapy with palbociclib in thyroid carcinoma with BRAF V600E

Oncotarget, 2017-10, Vol.8 (49), p.84743

2017

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Solitary Rectal Ulcer Syndrome in a Teenaged Boy

Journal of pediatric gastroenterology and nutrition, 1985-10, Vol.4 (5), p.835-838

1985

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EBV-positive, HHV8-negative large B-cell lymphoma with an unusual germinotropic growth pattern in an immunocompetent patient

Clinical case reports, 2018, Vol.6 (9), p.1818-1824

2018

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Phenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposis

American journal of human genetics, 1992-05, Vol.50 (5), p.988-997

1992

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Desbuquois syndrome: Clinical, radiographic, and morphologic characterization

American journal of medical genetics, 1994-08, Vol.52 (1), p.9-18

1994

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Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes

Human genetics, 1992-02, Vol.88 (4), p.393-398

1992

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Reply to Rivera

American journal of human genetics, 1993-08, Vol.53 (2), p.533-534

1993

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Small cell lung cancer cell line derived from a primary tumor with a characteristic deletion of 3p

Cancer research (Chicago, Ill.), 1987-04, Vol.47 (8), p.2148-2155

1987

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Pediatric residencies: differences between 1959/1960 and 1984/1985

Pediatrics (Evanston), 1988-11, Vol.82 (5), p.752

1988

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Solitary Rectal Ulcer Syndrome in a Teenaged Boy

Journal of pediatric gastroenterology and nutrition, 1985-01, Vol.4 (5), p.835-838

1985

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Marfan Syndrome Type II: There Is More to Marfan Syndrome than Fibrillin 1

Congenital Heart Disease, 2006, Vol.1 (5), p.229-232

2006

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Chromothriptic Cure of WHIM Syndrome

Incidence and patterns of ALK FISH abnormalities seen in a large unselected series of lung carcinomas

Distinct Missense Mutations of the FGFR3 Lys650 Codon Modulate Receptor Kinase Activation and the Severity of the Skeletal Dysplasia Phenotype

Challenging cases of follicular lymphoma diagnosed by core needle biopsy incorporating proliferation index and cytogenetics

Characteristics of myeloproliferative neoplasms in patients exposed to ionizing radiation following the Chernobyl nuclear accident

EBV ‐positive, HHV 8‐negative large B‐cell lymphoma with an unusual germinotropic growth pattern in an immunocompetent patient

EBV‐positive, HHV8‐negative large B‐cell lymphoma with an unusual germinotropic growth pattern in an immunocompetent patient

Vemurafenib-resistance via de novo RBM genes mutations and chromosome 5 aberrations is overcome by combined therapy with palbociclib in thyroid carcinoma with BRAFV600E

WHIM Syndrome Cured by Chromothripsis

Abstract 3093: Genomic characteristics of myeloproliferative neoplasms in patients exposed to ionizing radiation following the Chernobyl nuclear accident

Low expression of Abelson interactor-1 is linked to acquired drug resistance in Bcr-Abl-induced leukemia

Marfan Syndrome Type II: There Is More to Marfan Syndrome than Fibrillin 1

Genomic Characteristics of Myeloproliferative Neoplasms in Patients Exposed to Ionizing Radiation following the Chernobyl Nuclear Accident

Abstract B08: New Abelson interactor-1(Abi-1)-driven mechanism of acquired drug resistance

Vemurafenib-resistance via de novo RBM genes mutations and chromosome 5 aberrations is overcome by combined therapy with palbociclib in thyroid carcinoma with BRAF V600E

Solitary Rectal Ulcer Syndrome in a Teenaged Boy

EBV-positive, HHV8-negative large B-cell lymphoma with an unusual germinotropic growth pattern in an immunocompetent patient

Phenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposis

Desbuquois syndrome: Clinical, radiographic, and morphologic characterization

Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes

Reply to Rivera

Small cell lung cancer cell line derived from a primary tumor with a characteristic deletion of 3p

Pediatric residencies: differences between 1959/1960 and 1984/1985

Solitary Rectal Ulcer Syndrome in a Teenaged Boy

Marfan Syndrome Type II: There Is More to Marfan Syndrome than Fibrillin 1

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