Publications by authors named "Steven Klein"

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Corrigendum to "Shattering the STIGMA: Talking openly about MOUD in 12-step recovery programs" [Journal of Substance Use and Addiction Treatment, 181 (2026) 209829].
Steven Klein, Juan Franco, Adam Scioli

J Subst Use Addict Treat· December 2025

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Shattering the STIGMA: Talking openly about MOUD in 12-step recovery programs.
Steven Klein, Juan Franco, Adam Scioli

J Subst Use Addict Treat· November 2025

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Introduction to "Research that Transformed Developmental Biology".
Steven L Klein

Dev Biol· March 2025

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Phenotypic spectrum and tumor risk in Simpson-Golabi-Behmel syndrome: Case series and comprehensive literature review.
Alex F Nisbet, Aravind Viswanathan, Andrew M George, Pedro Arias, Steven D Klein

Am J Med Genet A· December 2024

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Update on Surveillance for Wilms Tumor and Hepatoblastoma in Beckwith-Wiedemann Syndrome and Other Predisposition Syndromes.
Jennifer M Kalish, Kerri D Becktell, Gaëlle Bougeard, Garrett M Brodeur, Lisa R Diller, Steven D Klein

Clin Cancer Res· December 2024

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Can glucose facilitate fear exposure? Randomized, placebo-controlled trials on the effects of glucose administration on fear extinction processes.
Alexander Hauck, Tanja Michael, Tobias C Issler, Steven Klein, Johanna Lass-Hennemann

Behav Res Ther· July 2024

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Bop1 is required to establish precursor domains of craniofacial tissues.
Stephanie Keer, Karen M Neilson, Helene Cousin, Himani D Majumdar, Dominique Alfandari, Steven L Klein

Genesis· February 2024

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The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains.
Alexander Marchak, Karen M Neilson, Himani D Majumdar, Kiyoshi Yamauchi, Steven L Klein

Dev Dyn· December 2023

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Overgrowth syndromes, diagnosis and management.
Steven D Klein, Alex Nisbet, Jennifer M Kalish

Curr Opin Pediatr· December 2023

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Occurrence of Hepatoblastomas in Patients with Beckwith-Wiedemann Spectrum (BWSp).
Steven D Klein, Madison DeMarchis, Rebecca L Linn, Suzanne P MacFarland, Jennifer M Kalish

Cancers (Basel)· April 2023

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Changes in Memory, Sedation, and Receptor Kinetics Imparted by the β2-N265M and β3-N265M GABA Receptor Point Mutations.
Alifayaz Abdulzahir, Steven Klein, Chong Lor, Mark G Perkins, Alyssa Frelka

Int J Mol Sci· March 2023

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Repressive Interactions Between Transcription Factors Separate Different Embryonic Ectodermal Domains.
Steven L Klein, Andre L P Tavares, Meredith Peterson, Charles H Sullivan, Sally A Moody

Front Cell Dev Biol· February 2022

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Epigenetic mosaicism and cell burden in Beckwith-Wiedemann syndrome due to loss of methylation at imprinting control region 2.
Kelly A Duffy, Evan R Hathaway, Steven D Klein, Arupa Ganguly, Jennifer M Kalish

Cold Spring Harb Mol Case Stud· December 2021

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Hotspot Mutations in DICER1 Causing GLOW Syndrome-Associated Macrocephaly Modulation of Specific microRNA Populations Result in the Activation of PI3K/ATK/mTOR Signaling.
Steven D Klein, Julian A Martinez-Agosto

Microrna· May 2021

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Transcriptome analysis of MBD5-associated neurodevelopmental disorder (MAND) neural progenitor cells reveals dysregulation of autism-associated genes.
Sureni V Mullegama, Steven D Klein, Stephen R Williams, Jeffrey W Innis, Frank J Probst

Sci Rep· May 2021

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Identifying surgeon and institutional drivers of cost in total shoulder arthroplasty: a multicenter study.
Michael P Carducci, Kuhan A Mahendraraj, Mariano E Menendez, Isaac Rosen, Steven M Klein

J Shoulder Elbow Surg· January 2021

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Natural size variation among embryos leads to the corresponding scaling in gene expression.
Avi Leibovich, Tamir Edri, Steven L Klein, Sally A Moody, Abraham Fainsod

Dev Biol· June 2020

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Mutations in the sonic hedgehog pathway cause macrocephaly-associated conditions due to crosstalk to the PI3K/AKT/mTOR pathway.
Steven D Klein, Dzung C Nguyen, Viraj Bhakta, Derek Wong, Vivian Y Chang

Am J Med Genet A· December 2019

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Mutations in STAG2 cause an X-linked cohesinopathy associated with undergrowth, developmental delay, and dysmorphia: Expanding the phenotype in males.
Sureni V Mullegama, Steven D Klein, Rebecca H Signer, , Eric Vilain

Mol Genet Genomic Med· February 2019

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The Role of Self-reports and Behavioral Measures of Interpretation Biases in Children with Varying Levels of Anxiety.
Anke M Klein, Emmelie Flokstra, Rianne van Niekerk, Steven Klein, Ronald M Rapee

Child Psychiatry Hum Dev· December 2018

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Is it time to retire fragile X testing as a first-tier test for developmental delay, intellectual disability, and autism spectrum disorder?
Sureni V Mullegama, Steven D Klein, Dzung C Nguyen, Arang Kim, Rebecca Signer

Genet Med· December 2017

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De novo loss-of-function variants in STAG2 are associated with developmental delay, microcephaly, and congenital anomalies.
Sureni V Mullegama, Steven D Klein, Milene V Mulatinho, Tharanga Niroshini Senaratne, Kathryn Singh

Am J Med Genet A· May 2017

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Sex-Specific Effects of Testosterone on the Sexually Dimorphic Transcriptome and Epigenome of Embryonic Neural Stem/Progenitor Cells.
Matthew S Bramble, Lara Roach, Allen Lipson, Neerja Vashist, Ascia Eskin, Steven Klein

Sci Rep· November 2016

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Truncating mutations in APP cause a distinct neurological phenotype.
Steven Klein, Alexander Goldman, Hane Lee, Shahnaz Ghahremani, Viraj Bhakta

Ann Neurol· September 2016

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Complications of Lower Body Lift Surgery in Postbariatric Patients.
Ingrid G M Poodt, Martine M van Dijk, Steven Klein, Maarten M Hoogbergen

Plast Reconstr Surg Glob Open· September 2016

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