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Literature library

Case Reports

Topic:

8

2022

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Case report: FOXP1 syndrome caused by a de novo splicing variant (c.1652+5 G>A) of the FOXP1 gene

Min Chen, 1 Yixi Sun, 1 Yeqing Qian, 1 Na Chen, 1 Hongge Li, 1 Liya Wang, 1 and Minyue Dongcorresponding

This paper explores various things

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Developmental biology

Topic:

2

2021

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Autism-linked gene FoxP1 selectively regulates the cultural transmission of learned vocalizations

F Garcia-Oscos 1, T M I Koch 1, H Pancholi 1, M Trusel 1, V Daliparthi 1, M Co 1, S E Park 1, F Ayhan 1, D H Alam 1, J E Holdway 1, G Konopka 1, T F Roberts 2

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Developmental biology

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12

2020

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Identification of FoxP circuits involved in locomotion and object fixation  in Drosophila 

Ottavia Palazzo 1, Mathias Rass 1, Björn Brembs 1 

This is a paper about neuro development

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Syndrome description

Topic:

9

2021

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Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptoms

M. Pilar Trelles, Tess Levy, Bonnie Lerman, Paige Siper, Reymundo Lozano, Danielle Halpern, Hannah Walker, Jessica Zweifach, Yitzchak Frank, Jennifer Foss-Feig, Alexander Kolevzon & Joseph Buxbaum

This study, conducted by the Seaver team, characterized the FOXP1 syndrome

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Syndrome description

Topic:

4

2021

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FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring

Reymundo Lozano, Catherine Gbekie, Paige M. Siper, Shubhika Srivastava, Jeffrey M. Saland, Swathi Sethuram, Lara Tang, Elodie Drapeau, Yitzchak Frank, Joseph D. Buxbaum & Alexander Kolevzon

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Transcriptional regulation

Topic:

2

2021

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Ensemble Switching of the DNA-Binding Domain of Human FOXP1

Narendar Kolimi, Exequiel Medina, Cesar Ramirez-Sarmiento, Hugo Sanabria, Jorge Babul

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Transcriptional regulation

Topic:

1

2021

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FOXP1 Interacts with MyoD to Repress its Transcription and Myoblast  Conversion 

Woodring E Wright 1, Chuan Li 2, Chang-Xue Zheng 3, Haley O Tucker 3

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Transcriptional regulation

Topic:

9

2020

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Intrinsically Disordered Regions of the DNA-Binding Domain of Human  FoxP1 Facilitate Domain Swapping 

ExequielMedina1PabloVillalobos1George L.Hamilton2ElizabethA.Komives3HugoSanabria2César A.Ramírez-Sarmiento45JorgeBabul1

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Z

Topic:

5

2021

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Severe speech impairment is a distinguishing feature of FOXP1-related disorder

Ruth O Braden, David J Amori, Simon E Fisher, Cristina Mei,
Candace T Muers, Heather Mefford, DeepakGill, Siddharth Srivastava,
Lindsay C Swanson, Himanshu Goel, Ingrid E Scheffer, Angela T Morgan

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Z

Topic:

4

2021

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A genome-wide association study identifies a gene network associated with paranoid schizophrenia and antipsychotics-induced tardive dyskinesia

Anastasia Levchenko 1, Alexander Kanapin 2, Anastasia Samsonova 2, Olga Yu Fedorenko 3, Elena G Kornetova 4, Timur Nurgaliev 5, Galina E Mazo 6, Arkadiy V Semke 7, Alexander O Kibitov 8, Nikolay A Bokhan 9, Raul R Gainetdinov 10, Svetlana A Ivanova 11

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Z

Topic:

12

2021

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Autism Spectrum Disorder (ASD) and Attention Deficit Hyperactivity Disorder (ADHD) With Language Impairment Accompanied by Developmental Disability Caused by Forkhead Box Protein 1 (FOXP1) Exon Deletion: A Case Report

Shuliweeh Alenezi, Ahmed Alyahya, Hesham Aldhalaan

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Z

Topic:

1

2021

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FOXP1 negatively regulates intrinsic excitability in D2 striatal projection  neurons by promoting inwardly rectifying and leak potassium currents 

Nitin Khandelwal 1, Sheridan Cavalier 1, Volodymyr Rybalchenko 1, Ashwinikumar  Kulkarni 1, Ashley G Anderson 1, Genevieve Konopka 2, Jay R Gibson 3 

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Z

Topic:

9

2020

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Peruvian Newborn Male with 3p13 Deletion Syndrome Encompassing  the FOXP1 Gene: Review of the Literature 

Hugo H. Abarca-Barriga 

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Z

Topic:

9

2020

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FOXP transcription factors in vertebrate brain development, function, and  disorders 

Marissa Co 1, Ashley G Anderson 2, Genevieve Konopka 2 

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Z

Topic:

3

2020

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Single-Cell Analysis of Foxp1-Driven Mechanisms Essential for Striatal  Development 

Ashley G Anderson 1, Ashwinikumar Kulkarni 1, Matthew Harper 1, Genevieve Konopka

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Z

Topic:

2

2020

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Foxp1 Regulates Neural Stem Cell Self-Renewal and Bias Toward Deep  Layer Cortical Fates 

Caroline Alayne Pearson 1, Destaye M Moore 1, Haley O Tucker 2, Joseph D Dekker 2, Hui  Hu 3, Amaya Miquelajáuregui 4, Bennett G Novitch 5 

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Z

Topic:

12

2020

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Coupling of autism genes to tissue-wide expression and dysfunction of  synapse, calcium signaling and transcriptional regulation 

Jamie Reilly, Louise Gallagher, Geraldine Leader, Sanbing Shen 

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Z

Topic:

11

2020

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Dysfunction of the corticostriatal pathway in autism spectrum disorders Wei Li 1, Lucas Pozzo-Miller 1 

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Z

Topic:

10

2020

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Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic  Urinary Tract Malformations 

Dervla M Connaughton et al. 

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Z

Topic:

1

2020

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FOXP transcription factors in vertebrate brain development, function, and  disorders 

Marissa Co Ashley G. Anderson Genevieve Konopka 

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