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Sarah Hudspeth Elsea, 56802 W Drew St, Houston, TX 77006

Sarah Elsea Phones & Addresses

802 W Drew St, Houston, TX 77006   

5935 Spellman Rd, Houston, TX 77096   

Nashville, TN   

Midlothian, VA   

4258 Cherry Hill Dr, Okemos, MI 48864    517-3474095   

869 Beechlawn Ct, East Lansing, MI 48823    517-3328137   

3800 Lenox Forest Dr, Midlothian, VA 23113   

Work

Position: Professional/Technical

Education

School / High School: Vanderbilt University

Languages

English

Awards

Healthgrades Honor Roll

Ranks

Certificate: Clinical Biochemical Genetics, 1999

Mentions for Sarah Hudspeth Elsea

Career records & work history

Medicine Doctors

Sarah Elsea Photo 1

Dr. Sarah H Elsea, Richmond VA - MD (Doctor of Medicine)

Specialties:
Clinical Biochemical Genetics
Address:
1101 E Marshall St, Richmond, VA 23298
804-6280987 (Phone) 804-6281609 (Fax)
Certifications:
Clinical Biochemical Genetics, 1999
Awards:
Healthgrades Honor Roll
Languages:
English
Education:
Medical School
Vanderbilt University

Sarah Elsea resumes & CV records

Resumes

Sarah Elsea Photo 13

Senior Director Biochemical Genetics

Location:
802 west Drew St, Houston, TX 77006
Industry:
Research
Work:
Baylor College of Medicine
Professor, Department of Molecular and Human Genetics
Baylor College of Medicine Jan 2013 - Mar 2017
Associate Professor, Senior Division Director of Biochemical Genetics
Baylor College of Medicine Jan 2013 - Mar 2017
Senior Director Biochemical Genetics
Virginia Commonwealth University Jan 1, 2004 - Dec 31, 2013
Associate Professor
Michigan State University Jan 1, 1998 - Jan 1, 2004
Assistant and Associate Professor
Education:
Missouri State University 2016 - 2019
Bachelors, Bachelor of Science
Vanderbilt University School of Medicine 1990 - 1994
Doctorates, Doctor of Philosophy, Biochemistry
Missouri State University 1986 - 1990
Bachelors, Bachelor of Science, Chemistry
Fort Osage Senior High
Fort Osage High School
Vanderbilt University
Doctorates, Doctor of Philosophy, Biochemistry
Skills:
Molecular Biology, Biochemistry, Genetics, Cell Biology, Pcr, Life Sciences, Research, Cell Culture, Molecular Genetics, Western Blotting, Science, Lifesciences, Genomics, Confocal Microscopy, Molecular Cloning, Dna, Polymerase Chain Reaction
Sarah Elsea Photo 14

Experienced Vendor Manager/Customer Services

Location:
Chicago, Illinois
Industry:
Consumer Services
Work:
Luke's Appraisal Service's, Inc. - Greater Chicago Area Jan 2013 - Feb 2013
Appraisal Coordinator
Equifax Settlement Services - Greater Pittsburgh Area Jul 2012 - Dec 2012
Vendor Management // Assignment Spcialist
UPMC - Greater Pittsburgh Area Jun 2008 - Apr 2012
Health Unit Coordinator
ZLB Plasma Services - Columbus, Ohio Area Jun 2007 - Jan 2008
BMT II
Speedway SuperAmerica LLC - Columbus, Ohio Area Apr 2007 - Sep 2007
Shift Leader
WBGU FM 88.1 - Bowling Green, Ohio Sep 2003 - Oct 2006
Radio Personality
Education:
Bowling Green State University 2002 - 2007
Bachelor's degree, Liberal Arts and Sciences/Liberal Studies
Skills:
Customer Service, Scheduling, Testing, Administration, People Skills, Education, Customer Focus, Mortgage Servicing, Radio, Media & Entertainment, Assignment, Vendor Management, Residential Mortgages
Interests:
New technology, reading (Mostly poetry, history, novels, science fiction/fantasy, and non-fiction.), art history, social networking, underground/underrepresented music, culture, psychology/behavioral science, health care reform, family, film, gourmet cooking/dining,

Publications & IP owners

Us Patents

Methods And Probes Relating To Smith-Magenis Syndrome And The Rai1 Gene

US Patent:
2004017, Sep 2, 2004
Filed:
Dec 24, 2003
Appl. No.:
10/746834
Inventors:
Sarah Elsea - Okemos MI, US
International Classification:
C12Q001/68
US Classification:
435/006000
Abstract:
Method and probes are disclosed to assist in the diagnosis of Smith-Magenis syndrome (SMS). These methods include the use of probes that are specific for the retinoic acid induced (RAI1) gene. The probes are added to a genetic sample from a subject and the presence or sence of the RAI1 gene is determined. Alternatively, the genetic sample from the subject is sequenced to determine whether there is a mutation in the RAI1 gene. The deletion or mutation of the RAI1 gene leads to most of the phenotypic features of SMS.

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