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Gmnc Is a Master Regulator of the Multiciliated Cell Differentiation Program

Current biology, 2015-12, Vol.25 (24), p.3267-3273

2015

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When bitcoin lost its position: Cryptocurrency uncertainty and the dynamic spillover among cryptocurrencies before and during the COVID-19 pandemic

International review of financial analysis, 2022-10, Vol.83, p.102309-102309, Article 102309

2022

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Impact of Mitochondrial Genetic Variants in ND1, ND2, ND5, and ND6 Genes on Sperm Motility and Intracytoplasmic Sperm Injection (ICSI) Outcomes

Reproductive sciences (Thousand Oaks, Calif.), 2021-05, Vol.28 (5), p.1540-1555

2021

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Long memory behavior in Singapore's tourism market

The international journal of tourism research, 2017-09, Vol.19 (5), p.524-534

2017

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Have the extraordinary circumstances of the COVID-19 outbreak and the Russian–Ukrainian conflict impacted the efficiency of cryptocurrencies?

Financial innovation (Heidelberg), 2024-12, Vol.10 (1), p.8-28, Article 8

2024

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A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability

eLife, 2018-05, Vol.7

2018

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Did real economic uncertainty drive risk connectedness in the oil–stock nexus during the COVID-19 outbreak? A partial wavelet coherence analysis

Journal of economic structures, 2023-12, Vol.12 (1), p.11-23, Article 11

2023

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Katanin p80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number

Neuron (Cambridge, Mass.), 2014-12, Vol.84 (6), p.1240-1257

2014

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A progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI‐NET sequencing

EMBO molecular medicine, 2023-02, Vol.15 (2), p.e16478-n/a

2023

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Skeletal phenotype/genotype in progressive pseudorheumatoid chondrodysplasia

Clinical rheumatology, 2020-02, Vol.39 (2), p.553-560

2020

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Clinical Phenotype and Bone Biopsy Characteristics in a Child with Proteus Syndrome

Calcified tissue international, 2021-11, Vol.109 (5), p.586-595

2021

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Recessive mutation in GALNT3 causes hyperphosphatemic familial tumoral calcinosis associated with chronic recurrent multifocal osteomyelitis

The Turkish journal of pediatrics, 2019-01, Vol.61 (1), p.130-133

2019

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Time-varying exchange rate exposure and exchange rate risk pricing in the Canadian Equity Market

Economic modelling, 2014-02, Vol.37, p.451-463

2014

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Case report: Dihydropyridine receptor ( CACNA1S ) congenital myopathy, a novel phenotype with early onset periodic paralysis

Frontiers in neurology, 2024-02, Vol.15, p.1359479

2024

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The influence of foreign direct investment on banking stability in a dual banking system during the COVID-19 pandemic and the global financial crisis

Borsa Istanbul Review, 2024-09, Vol.24 (5), p.1046-1058

2024

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Loss of CHSY1, a Secreted FRINGE Enzyme, Causes Syndromic Brachydactyly in Humans via Increased NOTCH Signaling

American journal of human genetics, 2010-12, Vol.87 (6), p.768-778

2010

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Plasma miRNAs as potential biomarkers for schizophrenia in a Jordanian cohort

Non-coding RNA research, 2024-06, Vol.9 (2), p.350-358

2024

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Long-Term Culture of Self-renewing Pancreatic Progenitors Derived from Human Pluripotent Stem Cells

Stem cell reports, 2017-06, Vol.8 (6), p.1675-1688

2017

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Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1

Nature genetics, 2012-06, Vol.44 (6), p.709-713

2012

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The Library's Role in Marketing Digital Information Services during COVID-19: Al-Balqa Applied University: Case Study

International journal of information science and management, 2024-07, Vol.22 (3), p.139-159

2024

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Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita

American journal of human genetics, 2017-04, Vol.100 (4), p.659-665

2017

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Information Needs: Developing Personas of Humanities Scholars

The Journal of academic librarianship, 2014-09, Vol.40 (5), p.500-509

2014

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Foreign exchange rate exposure: Evidence from Canada

Review of financial economics, 2014-01, Vol.23 (1), p.18-29

2014

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Tomographic Study of the Malformation Complex in Correlation With the Genotype in Patients With Robinow Syndrome: Review Article

JIM - high impact case reports, 2020, Vol.8, p.2324709620911771-2324709620911771

2020

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Torticollis in Connection with Spine Phenotype

Diagnostics (Basel), 2022-07, Vol.12 (7), p.1672

2022

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Gmnc Is a Master Regulator of the Multiciliated Cell Differentiation Program

When bitcoin lost its position: Cryptocurrency uncertainty and the dynamic spillover among cryptocurrencies before and during the COVID-19 pandemic

Impact of Mitochondrial Genetic Variants in ND1, ND2, ND5, and ND6 Genes on Sperm Motility and Intracytoplasmic Sperm Injection (ICSI) Outcomes

Long memory behavior in Singapore's tourism market

Have the extraordinary circumstances of the COVID-19 outbreak and the Russian–Ukrainian conflict impacted the efficiency of cryptocurrencies?

A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability

Did real economic uncertainty drive risk connectedness in the oil–stock nexus during the COVID-19 outbreak? A partial wavelet coherence analysis

Katanin p80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number

A progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI‐NET sequencing

Skeletal phenotype/genotype in progressive pseudorheumatoid chondrodysplasia

Clinical Phenotype and Bone Biopsy Characteristics in a Child with Proteus Syndrome

Recessive mutation in GALNT3 causes hyperphosphatemic familial tumoral calcinosis associated with chronic recurrent multifocal osteomyelitis

Time-varying exchange rate exposure and exchange rate risk pricing in the Canadian Equity Market

Case report: Dihydropyridine receptor ( CACNA1S ) congenital myopathy, a novel phenotype with early onset periodic paralysis

The influence of foreign direct investment on banking stability in a dual banking system during the COVID-19 pandemic and the global financial crisis

Loss of CHSY1, a Secreted FRINGE Enzyme, Causes Syndromic Brachydactyly in Humans via Increased NOTCH Signaling

Plasma miRNAs as potential biomarkers for schizophrenia in a Jordanian cohort

Long-Term Culture of Self-renewing Pancreatic Progenitors Derived from Human Pluripotent Stem Cells

Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1

The Library's Role in Marketing Digital Information Services during COVID-19: Al-Balqa Applied University: Case Study

Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita

Information Needs: Developing Personas of Humanities Scholars

Foreign exchange rate exposure: Evidence from Canada

Tomographic Study of the Malformation Complex in Correlation With the Genotype in Patients With Robinow Syndrome: Review Article

Torticollis in Connection with Spine Phenotype

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