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Birgit Funke
Birgit Funke
Associate Professor of Genetics and Genomic Sciences
Dirección de correo verificada de mssm.edu
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TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome
S Merscher, B Funke, JA Epstein, J Heyer, A Puech, MM Lu, RJ Xavier, ...
Cell 104 (4), 619-629, 2001
10692001
ACMG clinical laboratory standards for next-generation sequencing
HL Rehm, SJ Bale, P Bayrak-Toydemir, JS Berg, KK Brown, JL Deignan, ...
Genetics in medicine 15 (9), 733-747, 2013
10352013
Genetic misdiagnoses and the potential for health disparities
AK Manrai, BH Funke, HL Rehm, MS Olesen, BA Maron, P Szolovits, ...
New England Journal of Medicine 375 (7), 655-665, 2016
7012016
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples
R Walsh, KL Thomson, JS Ware, BH Funke, J Woodley, KJ McGuire, ...
Genetics in Medicine 19 (2), 192-203, 2017
6742017
A common molecular basis for rearrangement disorders on chromosome 22q11
L Edelmann, RK Pandita, E Spiteri, B Funke, R Goldberg, N Palanisamy, ...
Human molecular genetics 8 (7), 1157-1167, 1999
5521999
Assuring the quality of next-generation sequencing in clinical laboratory practice
AS Gargis, L Kalman, MW Berry, DP Bick, DP Dimmock, T Hambuch, F Lu, ...
Nature biotechnology 30 (11), 1033-1036, 2012
5032012
Cardiovascular pathology in Hutchinson-Gilford progeria: correlation with the vascular pathology of aging
M Olive, I Harten, R Mitchell, JK Beers, K Djabali, K Cao, MR Erdos, ...
Arteriosclerosis, thrombosis, and vascular biology 30 (11), 2301-2309, 2010
4252010
Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity
AA Alfares, MA Kelly, G McDermott, BH Funke, MS Lebo, SB Baxter, ...
Genetics in medicine 17 (11), 880-888, 2015
4242015
Using high-resolution variant frequencies to empower clinical genome interpretation
N Whiffin, E Minikel, R Walsh, AH O’Donnell-Luria, K Karczewski, AY Ing, ...
Genetics in Medicine 19 (10), 1151-1158, 2017
4172017
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing
TJ Pugh, MA Kelly, S Gowrisankar, E Hynes, MA Seidman, SM Baxter, ...
Genetics in Medicine 16 (8), 601-608, 2014
3602014
College of American Pathologists' laboratory standards for next-generation sequencing clinical tests
N Aziz, Q Zhao, L Bry, DK Driscoll, B Funke, JS Gibson, WW Grody, ...
Archives of Pathology and Laboratory Medicine 139 (4), 481-493, 2015
3582015
Evaluating the clinical validity of hypertrophic cardiomyopathy genes
J Ingles, J Goldstein, C Thaxton, C Caleshu, EW Corty, SB Crowley, ...
Circulation: Genomic and Precision Medicine 12 (2), e002460, 2019
3302019
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy …
MA Kelly, C Caleshu, A Morales, J Buchan, Z Wolf, SM Harrison, S Cook, ...
Genetics in Medicine 20 (3), 351-359, 2018
3302018
Best practices for benchmarking germline small-variant calls in human genomes
P Krusche, L Trigg, PC Boutros, CE Mason, FM De La Vega, BL Moore, ...
Nature biotechnology 37 (5), 555-560, 2019
3172019
Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era
P Teekakirikul, MA Kelly, HL Rehm, NK Lakdawala, BH Funke
The Journal of Molecular Diagnostics 15 (2), 158-170, 2013
2532013
Genetic variation in DTNBP1 influences general cognitive ability
KE Burdick, T Lencz, B Funke, CT Finn, PR Szeszko, JM Kane, ...
Human molecular genetics 15 (10), 1563-1568, 2006
2302006
Industrial Product-Service Systems (IPS2) Paradigm shift by mutually determined products and services
H Meier, O Völker, B Funke
The International Journal of Advanced Manufacturing Technology 52, 1175-1191, 2011
2162011
Association of the DTNBP1 locus with schizophrenia in a US population
B Funke, CT Finn, AM Plocik, S Lake, P DeRosse, JM Kane, ...
The American Journal of Human Genetics 75 (5), 891-898, 2004
2032004
Defining the genetic architecture of hypertrophic cardiomyopathy: re-evaluating the role of non-sarcomeric genes
R Walsh, R Buchan, A Wilk, S John, LE Felkin, KL Thomson, TH Chiaw, ...
European heart journal 38 (46), 3461-3468, 2017
2002017
A systematic approach to assessing the clinical significance of genetic variants
H Duzkale, J Shen, H McLaughlin, A Alfares, MA Kelly, TJ Pugh, ...
Clinical genetics 84 (5), 453-463, 2013
1962013
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
Artículos 1–20