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Job Posting: Full Stack Java Developer in Lafayette Louisiana

February 4, 2021 thinkgenetic Leave a Comment

No longer accepting applications Posted February 4, 2021 Job Overview We are expanding our efforts to shorten the time to diagnosis for rare genetic diseases by deploying our disease screening… CONTINUE

Filed Under: Career, Lafayette Tagged With: career, Java Developer, job, Lafayette

Job Posting: Full Stack Java Developer in Lafayette Louisiana

November 23, 2020 thinkgenetic Leave a Comment

ThinkGenetic Job Posting - Java Developer

No longer accepting applications Job Overview We are expanding our efforts to shorten the time to diagnosis for rare genetic diseases by deploying our disease screening algorithms on patient facing… CONTINUE

Filed Under: Career, Lafayette

Job Posting: Senior Data Engineer in Lafayette Louisiana

November 23, 2020 thinkgenetic Leave a Comment

ThinkGenetic Job Posting - Senior Data Engineer

No longer accepting applications Job Overview We are expanding our efforts to shorten the time to diagnosis for rare genetic diseases by applying our disease screening algorithms to de-identified patient… CONTINUE

Filed Under: Career, Lafayette Tagged With: career, job, Lafayette, Senior Data Engineer

Ruth O’Keefe Promoted to ThinkGenetic Vice President, Marketing and Patient Advocacy

April 2, 2019 thinkgenetic Leave a Comment

BOSTON, Ma., April 2, 2019 (Newswire.com) – ThinkGenetic, Inc. (www.ThinkGenetic.com), is excited to announce the promotion of Ruth O’Keefe to Vice President, Marketing and Patient Advocacy. ThinkGenetic, the creators of… CONTINUE

Filed Under: Advocacy, News, Press Tagged With: advocacy, Ruth O'Keefe, staff, ThinkGenetic

Recent ThinkGenetic.com Condition Additions for 08/29/2017

September 1, 2017 thinkgenetic Leave a Comment

ThinkGenetic strives to create, update, and review content regularly to ensure the information we provide is accurate, referenced, and available 24/7 to anyone searching for answers on genetic conditions and… CONTINUE

Filed Under: Updates Tagged With: AATD, Alpha-1-antitrypsin deficiency, SERPINA1

ThinkGenetic to Preview its SymptomMatcherTM Diagnostic Aid at NSGC 36th Annual Conference

August 16, 2017 thinkgenetic 1 Comment

ThinkGenetic leadership is looking forward to engaging with colleagues in the field at the National Society of Genetic Counselors (NSGC) 36th Annual Conference in Columbus, Ohio to help spread the… CONTINUE

Filed Under: Events Tagged With: Carol Ogg, Dawn Laney, Deepti Babu, genetic counselors, NSGC, Ruth O'Keefe

ThinkGenetic, Inc. Marketing Intern

August 14, 2017 thinkgenetic Leave a Comment

ThinkGenetic is looking for someone energetic, organized, and passionate about helping others  as our marketing intern. We are a fast-paced start-up working hard to increase awareness and traffic flow to… CONTINUE

Filed Under: Uncategorized

ThinkGenetic to Engage with Rare Disease Community at Global Genes’ 6th Annual RARE Patient Advocacy Summit

August 10, 2017 thinkgenetic Leave a Comment

ThinkGenetic, Inc. is delighted to be participating in the 6th Annual RARE Patient Advocacy Summit and Partnering and Investor Forum to further its mission of empowering the rare disease community… CONTINUE

Filed Under: Events Tagged With: artificial intelligence, Dave Jacob, Dawn Laney, Dekel Glebman, diagnosis, FDNA, Global Genes, rare patient advocacy summit

Care Day for Hereditary ATTR Amyloidosis Comes to Albany

August 4, 2017 thinkgenetic 1 Comment

Alnylam and ThinkGenetic are looking forward to another successful Care Day Event for hATTR amyloidosis in Albany, NY on the 12 of August. Come learn about topics relating to hATTR amyloidosis including: Disease… CONTINUE

Filed Under: Events Tagged With: Alnylam Pharmaceuticals, Amyloidosis, Carol Ogg, familial amyloidotic cardiomyopathy, familial amyloidotic polyneuropathy, hATTR amyloidosis, hereditary ATTR Amyloidosis, Janice Wiesman, Julia Wynn, partnership

Recent ThinkGenetic.com Condition Additions for 06/23/2017

June 23, 2017 thinkgenetic Leave a Comment

ThinkGenetic strives to create, update, and review content regularly to ensure the information we provide is accurate, referenced, and available 24/7 to anyone searching for answers on genetic conditions and… CONTINUE

Filed Under: Updates Tagged With: Argininemia, Charcot-Marie-Tooth disease, CMT, genetic condition, genetic disease, genetic disorder, genetic mutation, thinkgenetic.com

Genetic Condition Update for 06/02/2017

June 2, 2017 thinkgenetic Leave a Comment

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to anyone searching for answers on genetic diseases and… CONTINUE

Filed Under: Updates Tagged With: adenosine triphosphate, ATP, bones, brittle bone disease, creatine, dienoyl coa, dienoyl-coa reductase deficiency, fracture bones, GAMT, GAMT gene, genetic neurological disorder, Guanidinoacetate methyltransferase deficiency, neurologic disorder, OI, osteogenesis imperfecta, ovarian failure, Rare Disease, rare disorder, rare genetic disease, turner syndrome

Genetic Condition Update for Week of 04/24/2017

April 24, 2017 thinkgenetic Leave a Comment

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to anyone searching for answers on genetic diseases and… CONTINUE

Filed Under: Updates Tagged With: Acyl-coa dehydrogenase, HAE, Hereditary angioedema, MCAD

Genetic Condition Update for Week of 03/31/2017

March 31, 2017 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to anyone searching for answers on genetic diseases and… CONTINUE

Filed Under: Updates Tagged With: Fetal parvovirus, Hereditary hemorrhagic telangiectasia, HHT, Long-chain 3-hydroxyacyl-coa dehydrogenase deficiency, Lynch syndrome, Phenylketonuria, ThinkGenetic, tyrosinemia type 1, update

Genetic Condition Update for Week of 03/06/2017

March 6, 2017 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to anyone searching for answers on genetic diseases and… CONTINUE

Filed Under: Updates Tagged With: ADPKD, Amyloidosis, Autosomal dominant polycystic kidney disease, BOR syndrome, Branchiootic syndrome, Branchiootorenal syndrome, Familial transthyretin amyloidosis, genetic disease, MPS IVB, Mucopolysaccharidosis type ivb, rare genetic disorder, SCADD, Short chain acyl-CoA dehydrogenase deficiency

Rare Diseases Day 2017: The Cause & Celebrations

February 27, 2017 thinkgenetic Leave a Comment

Organized internationally by The European Organization (EURORDIS) for Rare Disorders and supported in the United States by the National Organization for Rare Disorders (NORD) and Global Genes, the last day… CONTINUE

Filed Under: Events Tagged With: #RareDiseaseDay, EURODIS, NORD, Rare Disease, Rare Disease Day

Site Update for Week of 01/17/2017

January 17, 2017 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to anyone searching for answers on genetic diseases and… CONTINUE

Filed Under: Updates Tagged With: genetic disorder, lysosomes, MCOLN1, Mucolipidosis, Mucolipidosis iv, Rare Disease

ThinkGenetic in 2016: A Message from the President

January 4, 2017 thinkgenetic 3 Comments

Preparing for this article on a year in the life of ThinkGenetic required the collection of statistics about financial and content contributors, website visitors, research and development activities, and partner… CONTINUE

Filed Under: News, Updates Tagged With: Amandeep Singh, Apache Solr, Carol Ogg, Daniel Jacob, Dave Jacob, Dawn Laney, diagnose genetic conditions, Emory University, Emory University’s Department of Human Genetics, genetic counselors, Graduate students, Human Phenotype Ontology, IBM Watson, Justin McGarvie, Len Barker, MD, Michael Gambello, Morgan Simmons, Peter Wilkerson, Pfizer, Robert Tomaino, Robin Vinson, Rokkit Marketing, Russell Weller, Ruth O'Keefe, Shire, Taylor Cassidy, The Legacy of Angels Foundation, ThinkGenetic Symptom Matcher, thinkgenetic.com, TLOAF, Xavier Mugaruza

ThinkGenetic to Attend the 35th Annual J.P. Morgan Healthcare Conference

December 13, 2016 thinkgenetic Leave a Comment

Westin St. Francis

Dave Jacob, Chief Executive Officer and Dawn Jacob Laney, MS, CGC, CCRC, Founder of ThinkGenetic, Inc., will be attending the 35th Annual J.P. Morgan Healthcare Conference on January 9 – 12, 2017 at… CONTINUE

Filed Under: Events Tagged With: 35th Annual J.P. Morgan Healthcare Conference, Dave Jacob, Dawn Jacob Laney, Dawn Laney, Healthcare Conference, J.P. Morgan, J.P. Morgan Healthcare Conference

Site Update for Week of 12/12/2016

December 13, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to anyone searching for answers on genetic diseases and… CONTINUE

Filed Under: Updates Tagged With: 15q24 deletion syndrome, 16p12.2 microdeletion syndrome, Beckwith-wiedemann syndrome, BRCA1, breast-ovarian cancer, CADASIL, Chromosome 16p12.2-p11.2 deletion syndrome, Chromosome 22q11.2 duplication, chromosomes, DNA, Down syndrome, Galactosemia, Pfeiffer syndrome, Phelan-McDermid Syndrome, protein, Xeroderma pigmentosum

ThinkGenetic at ACMG Annual Clinical Genetics Meeting 2017

December 12, 2016 thinkgenetic Leave a Comment

ThinkGenetic is pleased to be joining medical and clinical geneticists, genetic counselors, pediatric, obstetric, maternal fetal specialists, laboratory personnel, researchers and educators at the 2017 American College of Medical Genetics and… CONTINUE

Filed Under: Events Tagged With: ACMG, ACMG Annual Meeting, American College of Medical Genetics and Genomics, Annual Clinical Genetics Meeting, Exhibit

Site Update for Week of 12/01/2016

December 1, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to anyone searching for answers on genetic diseases and… CONTINUE

Filed Under: Updates Tagged With: Acromegaly, Acyl-coa dehydrogenase, ADAMTSL4, Agammaglobulinemia, Alagille syndrome, Alkaptonuria, Campomelic dysplasia, Cartilage-hair hypoplasia, Ceroid lipofuscinosis, CHARGE syndrome, chromosome pairs, congenital heart defect, developmental delay, DNA, enzyme, Fabry, Gal-1-PUT, galactose-1-phosphate uridyl transferase, Galactosemia, gene, genetic condition, glucose, Glutaric acidemia, glycogen storage disease, growth hormone, Huntington, hypogonadotropic hypogonadism, Kallman syndrome, Leopard syndrome, Mosaic trisomy 14, Noonan syndrome, Otosclerosis, Pitt-Hopkins syndrome, pituitary gland, protein, PTHS, Rare Disease, rare genetic disorder, Rett syndrome, Robinow syndrome, Sandhoff disease, Sickle cell anemia, Spinal muscular atrophy, Stickler syndrome, sugar, SYNGAP1, triple X syndrome, Trisomy 13, Trisomy x, webbed neck, XXX

Weekly Site Update for 11/15/2016

November 11, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to our audience. If you wish to see your… CONTINUE

Filed Under: Updates Tagged With: adrenal cortex, Alzheimer, Alzheimer disease, ARSA, arylsulfatase A, atrophy, Beckwith-wiedemann syndrome, Bilateral renal agenesis, biotin, biotinidase, Biotinidase deficiency, birth defects, CARASIL, Choroideremia, congenital, Congenital Adrenal Hyperplasia, Cutis Laxa, dementia, DMD, Duchenne muscular dystrophy, dystroglycanopathies, EIEE2, Epileptic encephalopathy, fetal varicella syndrome, genetic disorder, GM2, HD, Hirschsprung disease, Holocarboxylase synthetase deficiency, Huntington's disease, lactase, Lactase deficiency, metabolic condition, Metachromatic leukodystrophy, MLD, Mowat-Wilson syndrome, Mucolipidosis iii alpha, Mucolipidosis iii beta, muscle disorder, muscular dystrophy, neurologic disorder, polydystrophy, Retinitis pigmentosa, Rubinstein-Taybi syndrome, seizures, strokes, Tay-sachs disease, vision, Walker-Warburg syndrome, WWS, Xeroderma pigmentosum, XP

Rare is Everywhere – A Children’s Book to Inspire Our Differences

November 3, 2016 thinkgenetic 2 Comments

deborah-katz

by Deborah Katz, RN, MSN, Guest Contributor My new children’s book RARE IS EVERYWHERE is a book showcasing genetically rare animals like white tigers, blue lobsters, black jaguars and other amazing creatures to… CONTINUE

Filed Under: Education Tagged With: Deborah Katz, kickstarter, promo code, Rare Disease Foundation, Rare is Everywhere

Weekly Site Update for 10/25/2016

October 25, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to our audience. If you wish to see your… CONTINUE

Filed Under: Updates Tagged With: alpha-Gal, angiokeratomas, Barrett's esophagus, esophageal adenocarcinoma, Fabry disease, genetic condition, GLA gene, GNE Myopathy, GNEM, I-cell disease, Isovaleric acidemia, IVD gene, Leber hereditary optic neuropathy, Mucolipidosis ii alpha, Mucolipidosis ii beta, muscular dystrophy

Weekly Site Update for 10/18/2016

October 18, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to our audience. If you wish to see your… CONTINUE

Filed Under: Updates Tagged With: anchondrogensis, Houston-Harris, Langer-Saldino, Parenti-Fraccaro

Weekly Site Update for 10/03/2016

October 3, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to our audience. If you wish to see your… CONTINUE

Filed Under: Updates Tagged With: achondrogensis, Alpha-thalassemia, Andersen-Tawil Syndome, attention deficits, birth defects, Cardiofaciocutaneous syndrome, Congenital insensitivity to pain, cysts, Duchenne and becker muscular dystrophy, Familial adenomatous polyposis, GM2, hemangioblastomas, Hemophilia A, Hemophilia B, Hypophosphatasia, Lysosomal acid lipase deficiency, mood disorders, neurological, Phenylketonuria, Prader-willi syndrome, Roberts syndrome, Sotos syndrome, SYNGAP1, Tay-Sachs, tumors, VHL, Von Hippel-Lindau

Weekly Site Update for 09/26/2016

September 26, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to our audience. If you wish to see your… CONTINUE

Filed Under: Updates Tagged With: AIS, androgen insensitivity syndrome, fetal varicella syndrome, hutchinson-gilford progeria syndrome, Kabuki syndrome, KMT2D, maple syrup urine disease, MPS I, MPS III, MSUD, Mucopolysaccharidosis, ostosclerosis, progeria, SMA, Spinal muscular atrophy, Stickler syndrome

Weekly Site Update for 09/19/2016

September 19, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to our audience. If you wish to see your… CONTINUE

Filed Under: Updates Tagged With: Achondroplasia, dwarfism, Fabry, Fabry disease

Weekly Site Update for 09/12/2016

September 12, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to our audience. If you wish to see your… CONTINUE

Filed Under: Updates Tagged With: 2-Methyl-3-Hydroxybutryric acidemia deficiency, 2M3HBA, achondrogenesis, acromicria, ADAMTSL4, Aicardi, aicardi syndrome, alpha mannosidosis, Alpha-thalassemia, ALS, Alzheimer disease, Amyotrophic lateral sclerosis 1, and premature menopause syndrome, ARPKD, Autosomal recessive polycystic kidney disease, Barrett esophagus, CAH, CARASIL, Cartilage-hair hypoplasia, Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy, CHH, Congenital Adrenal Hyperplasia, Congenital insensitivity to pain, Congenital lactase deficiency, Cri-du-chat syndrome, DHMN5, Dihydrolipoamide dehydrogenase deficiency, Distal hereditary motor neuropathy, DLD, eye disorder, Fabry disease, Fetal parvovirus syndrome, Fetal trimethadione syndrome, Fragile x tremor/ataxia syndrome, FXTAS, GA-1, GA-2, Gaucher disease, genetic disease, genetic disorder, Glutaric acidemia, Glutaric acidemia type 1, Glutaric acidemia type 2, HD, Hereditary Diffuse Gastric Cancer, Hereditary polyneuropathy, Huntington's disease, intellectual disability, isoleucine, Li-fraumeni syndrome, Lundberg syndrome, mental retardation syndrom, Mitochondrial Neurogastrointestinal Encephalopathy, Mucopolysaccharidosis type (MPS) IV, Muir-Torre syndrome, NBS, Nemaline Myopathy, Neuronal ceroid lipofuscinosis, Nijmegen breakage syndrome, Ornithine Transcarbamylase Deficiency, Thalidomide embryopathy, Tridione, Trisomy 20p, Trisomy 8q, type V, x-linked, X-linked juvenile retinoschisis

Weekly Site Update for 09/06/2016

September 6, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to our audience. If you wish to see your… CONTINUE

Filed Under: Updates Tagged With: abnormalities, autism, dysplasia, Fragile X, Fragile X syndrome, Gaucher, Gaucher disease, GBA, Robinow, Robinow syndrome

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