Literature DB >> 19630565

Genetics, medicine, and the Plain people.

Kevin A Strauss1, Erik G Puffenberger.   

Abstract

The Old Order Amish and Old Order Mennonite populations of Pennsylvania are descended from Swiss Anabaptist immigrants who came to the New World in the early eighteenth century. Today they live in many small endogamous demes across North America. Genetically, these demes have dissimilar allele frequencies and disease spectra owing to unique founders. Biological and social aspects of Old Order communities make them ideal for studies in population genetics and genomic medicine, and over the last 40 years, advances in genomic science coincided with investigational studies in Plain populations. Newer molecular genetic technologies are sufficiently informative, rapid, and flexible to use in a clinical setting, and we have successfully integrated these tools into a rural pediatric practice. Our studies with the Pennsylvania Plain communities show that population-specific genetic knowledge provides a powerful framework in which to prevent disease, reduce medical costs, and create new insights into human biology.

Entities:  

Mesh:

Year:  2009        PMID: 19630565     DOI: 10.1146/annurev-genom-082908-150040

Source DB:  PubMed          Journal:  Annu Rev Genomics Hum Genet        ISSN: 1527-8204            Impact factor:   8.929


  35 in total

1.  Charting the Y-chromosome ancestry of present-day Argentinean Mennonites.

Authors:  Ulises Toscanini; Francesca Brisighelli; Cintia Llull; Gabriela Berardi; Andrea Gómez; Fernando Andreatta; Jacobo Pardo-Seco; Alberto Gómez-Carballa; Federico Martinón-Torres; Vanesa Álvarez-Iglesias; Antonio Salas
Journal:  J Hum Genet       Date:  2016-02-04       Impact factor: 3.172

2.  One community's effort to control genetic disease.

Authors:  Kevin A Strauss; Erik G Puffenberger; D Holmes Morton
Journal:  Am J Public Health       Date:  2012-05-17       Impact factor: 9.308

3.  Human ITCH E3 ubiquitin ligase deficiency causes syndromic multisystem autoimmune disease.

Authors:  Naomi J Lohr; Jean P Molleston; Kevin A Strauss; Wilfredo Torres-Martinez; Eric A Sherman; Robert H Squires; Nicholas L Rider; Kudakwashe R Chikwava; Oscar W Cummings; D Holmes Morton; Erik G Puffenberger
Journal:  Am J Hum Genet       Date:  2010-02-18       Impact factor: 11.025

4.  Deciphering the fine-structure of tribal admixture in the Bedouin population using genomic data.

Authors:  B Markus; I Alshafee; O S Birk
Journal:  Heredity (Edinb)       Date:  2013-10-02       Impact factor: 3.821

5.  Health Needs Assessment of Plain Populations in Lancaster County, Pennsylvania.

Authors:  Kirk Miller; Berwood Yost; Christina Abbott; Scottie Thompson; Emily Dlugi; Zachary Adams; Meryl Schulman; Nicole Strauss
Journal:  J Community Health       Date:  2017-02

6.  Newborn Screening for Inherited Metabolic Disorders: Early Identification and Long-Term Care for Patients in the Plain Community, Wisconsin, 2011-2017.

Authors:  Patrice K Held; Gregory M Rice; Ashley Kuhl; Nicoletta Drilias; Mei Baker; James Deline; Gretchen Spicer; Claire Sandrock; Christine M Seroogy; Jessica Scott Schwoerer
Journal:  Public Health Rep       Date:  2019 Nov/Dec       Impact factor: 2.792

7.  Homozygous frameshift mutation in TMCO1 causes a syndrome with craniofacial dysmorphism, skeletal anomalies, and mental retardation.

Authors:  Baozhong Xin; Erik G Puffenberger; Susan Turben; Haiyan Tan; Aimin Zhou; Heng Wang
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-14       Impact factor: 11.205

Review 8.  Amish revisited: next-generation sequencing studies of psychiatric disorders among the Plain people.

Authors:  Liping Hou; Gloria Faraci; David T W Chen; Layla Kassem; Thomas G Schulze; Yin Yao Shugart; Francis J McMahon
Journal:  Trends Genet       Date:  2013-02-17       Impact factor: 11.639

9.  Primary ciliary dyskinesia-causing mutations in Amish and Mennonite communities.

Authors:  Thomas W Ferkol; Erik G Puffenberger; Hauw Lie; Cynthia Helms; Kevin A Strauss; Anne Bowcock; John L Carson; Milan Hazucha; D Holmes Morton; Anand C Patel; Margaret W Leigh; Michael R Knowles; Maimoona A Zariwala
Journal:  J Pediatr       Date:  2013-03-07       Impact factor: 4.406

10.  Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup.

Authors:  Kevin A Strauss; Lauren DuBiner; Mariella Simon; Michael Zaragoza; Partho P Sengupta; Peng Li; Navneet Narula; Sandra Dreike; Julia Platt; Vincent Procaccio; Xilma R Ortiz-González; Erik G Puffenberger; Richard I Kelley; D Holmes Morton; Jagat Narula; Douglas C Wallace
Journal:  Proc Natl Acad Sci U S A       Date:  2013-02-11       Impact factor: 11.205

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