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Loss-of-Function Mutations in Growth Differentiation Factor-1 ( GDF1) Are Associated with Congenital Heart Defects in Humans

American journal of human genetics, 2007-11, Vol.81 (5), p.987-994

2007

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Novel mutation in sonic hedgehog in non-syndromic colobomatous microphthalmia

American journal of medical genetics. Part A, 2003-01, Vol.116A (3), p.215-221

2003

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Undifferentiated duodenal sarcoma with rhabdoid features

Journal of pediatric surgery case reports, 2020-07, Vol.58, p.101451, Article 101451

2020

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Outcome of biliary atresia after Kasai’s portoenterostomy: A 15-year experience

Indian pediatrics, 2017-04, Vol.54 (4), p.291-294

2017

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Tubular Colonic Duplication Presenting as Rectovestibular Fistula

Pediatric Gastroenterology, 2015, Hepatology & Nutrition, 18(3), , pp.197-201

2015

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A High-Density Genome Scan Detects Evidence for a Bipolar-Disorder Susceptibility Locus on 13q32 and Other Potential Loci on 1q32 and 18p11.2

Proceedings of the National Academy of Sciences - PNAS, 1999-05, Vol.96 (10), p.5604-5609

1999

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P24.14 Validation of Companion Diagnostics for the Identification of Patients with EGFR Exon20ins NSCLC for Amivantamab Therapy

Journal of thoracic oncology, 2021-10, Vol.16 (10), p.S1036-S1036

2021

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Subtotal Pancreatectomy for Congenital Hyperinsulinism: Our Experience and Review of Literature

Indian journal of surgery, 2015-12, Vol.77 (Suppl 3), p.778-782

2015

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1P Real-world frequency of non-small cell lung cancer with epidermal growth factor receptor (EGFR) exon 20 insertion (Exon20ins) mutations by site of insertion

Journal of thoracic oncology, 2021-04, Vol.16 (4), p.S699-S699

2021

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P76.74 PAPILLON: Randomized Phase 3 Study of Amivantamab Plus Chemotherapy vs Chemotherapy Alone in EGFR Exon20ins NSCLC

Journal of thoracic oncology, 2021-03, Vol.16 (3), p.S621-S621

2021

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P76.73 MARIPOSA: Randomized Phase 3 Study of First-line Amivantamab + Lazertinib vs Osimertinib vs Lazertinib in EGFR-mutant NSCLC

Journal of thoracic oncology, 2021-03, Vol.16 (3), p.S620-S621

2021

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Genomic structure and novel variants of myo-inositol monophosphatase 2 (IMPA2)

Molecular psychiatry, 2000-03, Vol.5 (2), p.165-171

2000

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Association study on the DUSP6 gene, an affective disorder candidate gene on 12q23, performed by using fluorescence resonance energy transfer-based melting curve analysis on the LightCycler

Molecular psychiatry, 2000-09, Vol.5 (5), p.489-494

2000

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Molecular cytogenetic fingerprinting of esophageal squamous cell carcinoma by comparative genomic hybridization reveals a consistent pattern of chromosomal alterations

Genes chromosomes & cancer, 1999-06, Vol.25 (2), p.160-168

1999

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Acute acalculous cholecystitis causing gall bladder perforation in children

Journal of Indian Association of Pediatric Surgeons, 2010-10, Vol.15 (4), p.139-141

2010

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The genomic structure, chromosomal localization, and analysis of SIL as a candidate gene for holoprosencephaly

Cytogenetic and genome research, 2002-01, Vol.97 (1-2), p.62-67

2002

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Post meningocele repair urinary ascites in a neonate—a rare presentation

Journal of pediatric surgery, 2012-05, Vol.47 (5), p.e33-e38

2012

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Refinement of Regions with Allelic Loss on Chromosome 18p11.2 and 18q12.2 in Esophageal Squamous Cell Carcinoma

Clinical cancer research, 2000-09, Vol.6 (9), p.3565-3569

2000

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Utility of a targeted NGS oncology assay for circulating tumor DNA in a multi-histology clinical setting

Annals of oncology, 2016-10, Vol.27, p.vi401-vi401

2016

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Analysis of Sciellin (SCEL) as a Candidate Gene in Esophageal Squamous Cell Carcinoma

Anticancer research, 2004-05, Vol.24 (3A), p.1417-1419

2004

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Radiation hybrid mapping of genes in the lithium-sensitive Wnt signaling pathway

Molecular psychiatry, 1999-09, Vol.4 (5), p.437-442

1999

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Phase 2 Trial of the Farnesyltransferase Inhibitor Tipifarnib in Previously Untreated Older Adults with AML and Baseline Presence of a Specific 2-Gene Expression Signature Ratio

Blood, 2012-11, Vol.120 (21), p.1508-1508

2012

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Abstract P5-01-09: Identification of Molecular Apocrine Triple Negative Breast Cancer Using a Novel 2-Gene Assay and Comparison with Androgen Receptor Protein Expression and Gene Expression Profiling by DASL

Cancer research (Chicago, Ill.), 2012-12, Vol.72 (24_Supplement), p.P5-P5-01-09

2012

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CFC1 Mutations in Patients with Transposition of the Great Arteries and Double-Outlet Right Ventricle

American journal of human genetics, 2002-03, Vol.70 (3), p.776-780

2002

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Loss-of-Function Mutations in Growth Differentiation Factor-1 ( GDF1) Are Associated with Congenital Heart Defects in Humans

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication

Novel mutation in sonic hedgehog in non-syndromic colobomatous microphthalmia

Undifferentiated duodenal sarcoma with rhabdoid features

Outcome of biliary atresia after Kasai’s portoenterostomy: A 15-year experience

Tubular Colonic Duplication Presenting as Rectovestibular Fistula

A High-Density Genome Scan Detects Evidence for a Bipolar-Disorder Susceptibility Locus on 13q32 and Other Potential Loci on 1q32 and 18p11.2

P24.14 Validation of Companion Diagnostics for the Identification of Patients with EGFR Exon20ins NSCLC for Amivantamab Therapy

Subtotal Pancreatectomy for Congenital Hyperinsulinism: Our Experience and Review of Literature

1P Real-world frequency of non-small cell lung cancer with epidermal growth factor receptor (EGFR) exon 20 insertion (Exon20ins) mutations by site of insertion

P76.74 PAPILLON: Randomized Phase 3 Study of Amivantamab Plus Chemotherapy vs Chemotherapy Alone in EGFR Exon20ins NSCLC

P76.73 MARIPOSA: Randomized Phase 3 Study of First-line Amivantamab + Lazertinib vs Osimertinib vs Lazertinib in EGFR-mutant NSCLC

Genomic structure and novel variants of myo-inositol monophosphatase 2 (IMPA2)

Association study on the DUSP6 gene, an affective disorder candidate gene on 12q23, performed by using fluorescence resonance energy transfer-based melting curve analysis on the LightCycler

Molecular cytogenetic fingerprinting of esophageal squamous cell carcinoma by comparative genomic hybridization reveals a consistent pattern of chromosomal alterations

Acute acalculous cholecystitis causing gall bladder perforation in children

The genomic structure, chromosomal localization, and analysis of SIL as a candidate gene for holoprosencephaly

Post meningocele repair urinary ascites in a neonate—a rare presentation

Refinement of Regions with Allelic Loss on Chromosome 18p11.2 and 18q12.2 in Esophageal Squamous Cell Carcinoma

Utility of a targeted NGS oncology assay for circulating tumor DNA in a multi-histology clinical setting

Analysis of Sciellin (SCEL) as a Candidate Gene in Esophageal Squamous Cell Carcinoma

Radiation hybrid mapping of genes in the lithium-sensitive Wnt signaling pathway

Phase 2 Trial of the Farnesyltransferase Inhibitor Tipifarnib in Previously Untreated Older Adults with AML and Baseline Presence of a Specific 2-Gene Expression Signature Ratio

Abstract P5-01-09: Identification of Molecular Apocrine Triple Negative Breast Cancer Using a Novel 2-Gene Assay and Comparison with Androgen Receptor Protein Expression and Gene Expression Profiling by DASL

CFC1 Mutations in Patients with Transposition of the Great Arteries and Double-Outlet Right Ventricle

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