Ingrid S. Paine - Concepedia

Author

Ingrid S. Paine

Baylor College of Medicine ORCID

Also Known As

I. Paine, Ingrid Paine, Ingrid S Paine, Ingrid S. Paine, Ingrid Sophie Paine, Justin Paschall

Publications

663

Citations

H-Index

Concepts

All Affiliations

Baylor College of Medicine The University of Texas Health Science Center at Houston Texas Children's Hospital Baylor Genetics Istanbul University

About

Ingrid S. Paine is an author at Baylor College of Medicine specializing in medicine, genetics, and morphogenesis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	304
2	Pathology	2	2	122
3	Engineering	1	1	55
4	Cell Biology	1	1	55
5	Cellular Physiology	1	1	55

Ingrid S. Paine

Publications

400

Citations

H-Index

Page 1

	Year	Citations
Paralog Studies Augment Gene Discovery: DDX and DHX Genes Ingrid S. Paine, Jennifer E. Posey, Christopher M. Grochowski, The American Journal of Human Genetics Functional GenomicsMedicineGeneticsGene CharacterizationPathway Analysis	2019	105
Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis Nuriye Dinçkan, Renqian Du, Lauren E. Petty, Journal of Dental Research BioinformaticsNext-generation SequencingGeneticsPathogenesisTooth Agenesis	2017	64
REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis Yavuz Bayram, Janson J. White, Nursel Elçioğlu, The American Journal of Human Genetics FibrosisMendelian DisorderGeneticsPathologyMedicine	2017	58
A Geometrically-Constrained Mathematical Model of Mammary Gland Ductal Elongation Reveals Novel Cellular Dynamics within the Terminal End Bud Ingrid S. Paine, Arnaud Chauvière, John D. Landua, PLoS Computational Biology EngineeringGeometrically-constrained Mathematical ModelTerminal End BudCytoskeletonCell Growth	2016	55
Functional biology of the Steel syndrome founder allele and evidence for clan genomics derivation of COL27A1 pathogenic alleles worldwide Claudia Gonzaga‐Jauregui, Gözde Yeşil, Harikiran Nistala, European Journal of Human Genetics	2020	37
<scp>Wolff–Parkinson–White</scp> syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation Zeynep Coban‐Akdemir, Wu‐Lin Charng, Mahshid S. Azamian, American Journal of Medical Genetics Part A	2020	36
Prioritization of Candidate Genes for Congenital Diaphragmatic Hernia in a Critical Region on Chromosome 4p16 using a Machine-Learning Algorithm Ian M. Campbell, Samantha Stover, Andrés Hernández, Journal of Pediatric Genetics	2018	23
The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia Valerie K. Jordan, T. Beck, Andrés Hernández, Human Molecular Genetics Developmental AnomalyDevelopmental BiologyMendelian DisorderCongenital Diaphragmatic HerniaGenetic Disorder	2018	22

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