| Year |
Citation |
Score |
| 2024 |
Ma M, Ganapathi M, Zheng Y, Tan KL, Kanca O, Bove KE, Quintanilla N, Sag SO, Temel SG, LeDuc CA, McPartland AJ, Pereira EM, Shen Y, Hagen J, Thomas CP, ... ... Wangler MF, et al. Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101125. PMID 38522068 DOI: 10.1016/j.gim.2024.101125 |
0.789 |
|
| 2024 |
Pan X, Tao AM, Lu S, Ma M, Hannan SB, Slaugh R, Drewes Williams S, O'Grady L, Kanca O, Person R, Carter MT, Platzer K, Schnabel F, Abou Jamra R, Roberts AE, ... ... Wangler MF, et al. De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features. American Journal of Human Genetics. PMID 38479391 DOI: 10.1016/j.ajhg.2024.02.007 |
0.86 |
|
| 2024 |
Vuocolo B, German RJ, Lalani SR, Murali CN, Bacino CA, Baskin S, Littlejohn R, Odom JD, McLean S, Schmid C, Nutter M, Stuebben M, Magness E, Juarez O, El Achi D, ... ... Wangler M, et al. Improving access to exome sequencing in a medically underserved population through the Texome Project. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101102. PMID 38431799 DOI: 10.1016/j.gim.2024.101102 |
0.436 |
|
| 2024 |
Dutta D, Kanca O, Shridharan RV, Marcogliese PC, Steger B, Morimoto M, Frost FG, Macnamara E, Wangler MF, Yamamoto S, Jenny A, Adams D, Malicdan MC, Bellen HJ. Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability. Proceedings of the National Academy of Sciences of the United States of America. 121: e2322582121. PMID 38381787 DOI: 10.1073/pnas.2322582121 |
0.807 |
|
| 2024 |
Ma M, Zheng Y, Lu S, Pan X, Worley KC, Burrage LC, Blieden LS, Allworth A, Chen WL, Merla G, Mandriani B, Rosenfeld JA, Li-Kroeger D, Dutta D, Yamamoto S, ... Wangler MF, et al. variants in are associated with hearing impairment, ocular pathology, and cardiac defects. Medrxiv : the Preprint Server For Health Sciences. PMID 38260438 DOI: 10.1101/2024.01.08.23300523 |
0.827 |
|
| 2023 |
Nil Z, Deshwar AR, Huang Y, Barish S, Zhang X, Choufani S, Le Quesne Stabej P, Hayes I, Yap P, Haldeman-Englert C, Wilson C, Prescott T, Tveten K, Vøllo A, Haynes D, ... ... Wangler MF, et al. Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies. American Journal of Human Genetics. PMID 37827158 DOI: 10.1016/j.ajhg.2023.09.009 |
0.812 |
|
| 2023 |
Yamamoto S, Kanca O, Wangler MF, Bellen HJ. Integrating non-mammalian model organisms in the diagnosis of rare genetic diseases in humans. Nature Reviews. Genetics. PMID 37491400 DOI: 10.1038/s41576-023-00633-6 |
0.786 |
|
| 2023 |
Guichard A, Lu S, Kanca O, Bressan D, Huang Y, Ma M, Sanz Juste S, Andrews JC, Jay KL, Sneider M, Schwartz R, Huang MC, Bei D, Pan H, Ma L, ... ... Wangler MF, et al. A comprehensive Drosophila resource to identify key functional interactions between SARS-CoV-2 factors and host proteins. Cell Reports. 42: 112842. PMID 37480566 DOI: 10.1016/j.celrep.2023.112842 |
0.796 |
|
| 2023 |
Jangam SV, Briere LC, Jay KL, Andrews JC, Walker MA, Rodan LH, High FA, Yamamoto S, Sweetser DA, Wangler MF. A de novo missense variant in EZH1 associated with developmental delay exhibits functional deficits in Drosophila melanogaster. Genetics. PMID 37314226 DOI: 10.1093/genetics/iyad110 |
0.565 |
|
| 2023 |
Tepe B, Macke EL, Niceta M, Weisz Hubshman M, Kanca O, Schultz-Rogers L, Zarate YA, Schaefer GB, Granadillo De Luque JL, Wegner DJ, Cogne B, Gilbert-Dussardier B, Le Guillou X, Wagner EJ, Pais LS, ... ... Wangler MF, et al. Bi-allelic variants in INTS11 are associated with a complex neurological disorder. American Journal of Human Genetics. PMID 37054711 DOI: 10.1016/j.ajhg.2023.03.012 |
0.768 |
|
| 2023 |
Andrews JC, Mok JW, Kanca O, Jangam S, Tifft C, Macnamara EF, Russell BE, Wang LK, Nelson SF, Bellen HJ, Yamamoto S, Malicdan MCV, Wangler MF. De Novo Variants in MRTFB have gain of function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100833. PMID 37013900 DOI: 10.1016/j.gim.2023.100833 |
0.771 |
|
| 2023 |
Jangam S, Briere LC, Jay K, Andrews JC, Walker MA, Rodan LH, High FA, Yamamoto S, Sweetser DA, Wangler M. A missense variant in associated with developmental delay exhibits functional deficits in . Medrxiv : the Preprint Server For Health Sciences. PMID 36778246 DOI: 10.1101/2023.01.31.23285113 |
0.821 |
|
| 2022 |
Huang Y, Lemire G, Briere LC, Liu F, Wessels MW, Wang X, Osmond M, Kanca O, Lu S, High FA, Walker MA, Rodan LH, Wangler MF, Yamamoto S, Kernohan KD, et al. The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability. American Journal of Human Genetics. 109: 2092. PMID 36332614 DOI: 10.1016/j.ajhg.2022.10.001 |
0.773 |
|
| 2022 |
Lu S, Ma M, Mao X, Bacino CA, Jankovic J, Sutton VR, Bartley JA, Wang X, Rosenfeld JA, Beleza-Meireles A, Chauhan J, Pan X, Li M, Liu P, Prescott K, ... ... Wangler MF, et al. De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement. American Journal of Human Genetics. 109: 1932-1943. PMID 36206744 DOI: 10.1016/j.ajhg.2022.09.005 |
0.804 |
|
| 2022 |
Gofin Y, Zhao X, Gerard A, Scaglia F, Wangler MF, Schrier Vergano SA, Scott DA. Evidence for an association between Coffin-Siris syndrome and congenital diaphragmatic hernia. American Journal of Medical Genetics. Part A. PMID 35796094 DOI: 10.1002/ajmg.a.62889 |
0.381 |
|
| 2022 |
Barish S, Senturk M, Schoch K, Minogue AL, Lopergolo D, Fallerini C, Harland J, Seemann JH, Stong N, Kranz PG, Kansagra S, Mikati MA, Jasien J, El-Dairi M, Galluzzi P, ... ... Wangler MF, et al. The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder. Human Molecular Genetics. PMID 35405010 DOI: 10.1093/hmg/ddac085 |
0.64 |
|
| 2022 |
Deisseroth CA, Lerma VC, Magyar CL, Pfliger JM, Nayak A, Bliss ND, LeMaire AW, Narayanan V, Balak C, Zanni G, Valente EM, Bertini E, Benke PJ, Wangler MF, Chao HT. An integrated phenotypic and genotypic approach reveals a high-risk subtype association for EBF3 missense variants affecting the zinc finger domain. Annals of Neurology. PMID 35340043 DOI: 10.1002/ana.26359 |
0.586 |
|
| 2022 |
Marcogliese PC, Deal SL, Andrews J, Harnish JM, Bhavana VH, Graves HK, Jangam S, Luo X, Liu N, Bei D, Chao YH, Hull B, Lee PT, Pan H, Bhadane P, ... ... Wangler MF, et al. Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases. Cell Reports. 38: 110517. PMID 35294868 DOI: 10.1016/j.celrep.2022.110517 |
0.78 |
|
| 2022 |
Harnish JM, Li L, Rogic S, Poirier-Morency G, Kim SY, Network UD, Boycott KM, Wangler MF, Bellen HJ, Hieter P, Pavlidis P, Liu Z, Yamamoto S. ModelMatcher: A scientist-centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease research. Human Mutation. PMID 35224820 DOI: 10.1002/humu.24364 |
0.593 |
|
| 2022 |
Sharma S, Hourigan B, Patel Z, Rosenfeld JA, Chan KM, Wangler MF, Yi JS, Lehman A, Horvath G, Cloos PA, Tan Q. Novel CIC variants identified in individuals with neurodevelopmental phenotypes. Human Mutation. PMID 35165976 DOI: 10.1002/humu.24346 |
0.402 |
|
| 2021 |
Khayat MM, Hu J, Jiang Y, Li H, Chander V, Dawood M, Hansen AW, Li S, Friedman J, Cross L, Bijlsma EK, Ruivenkamp CAL, Sansbury FH, Innis JW, O'Shea JO, ... ... Wangler MF, et al. missense mutations in Xia-Gibbs syndrome. Hgg Advances. 2. PMID 34950897 DOI: 10.1016/j.xhgg.2021.100049 |
0.355 |
|
| 2021 |
Manor J, Chung H, Bhagwat PK, Wangler MF. ABCD1 and X-linked adrenoleukodystrophy: A disease with a markedly variable phenotype showing conserved neurobiology in animal models. Journal of Neuroscience Research. PMID 34716609 DOI: 10.1002/jnr.24953 |
0.753 |
|
| 2021 |
Goodman LD, Cope H, Nil Z, Ravenscroft TA, Charng WL, Lu S, Tien AC, Pfundt R, Koolen DA, Haaxma CA, Veenstra-Knol HE, Wassink-Ruiter JSK, Wevers MR, Jones M, Walsh LE, ... ... Wangler MF, et al. TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila. American Journal of Human Genetics. PMID 34314705 DOI: 10.1016/j.ajhg.2021.06.019 |
0.772 |
|
| 2021 |
Ravenscroft TA, Phillips JB, Fieg E, Bajikar SS, Peirce J, Wegner J, Luna AA, Fox EJ, Yan YL, Rosenfeld JA, Zirin J, Kanca O, Benke PJ, Cameron ES, ... ... Wangler MF, et al. Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 34113007 DOI: 10.1038/s41436-021-01216-8 |
0.831 |
|
| 2021 |
Baldridge D, Wangler MF, Bowman AN, Yamamoto S, Schedl T, Pak SC, Postlethwait JH, Shin J, Solnica-Krezel L, Bellen HJ, Westerfield M. Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision. Orphanet Journal of Rare Diseases. 16: 206. PMID 33962631 DOI: 10.1186/s13023-021-01839-9 |
0.62 |
|
| 2021 |
Luo X, Schoch K, Jangam SV, Bhavana VH, Graves HK, Kansagra S, Jasien J, Stong N, Keren B, Mignot C, Ravelli C, Bellen HJ, Wangler MF, Shashi V, et al. Rare deleterious de novo missense variants in RNF2/RING2 are associated with a neurodevelopmental disorder with unique clinical features. Human Molecular Genetics. PMID 33864376 DOI: 10.1093/hmg/ddab110 |
0.674 |
|
| 2021 |
Hansen AW, Arora P, Khayat MM, Smith LJ, Lewis AM, Rossetti LZ, Jayaseelan J, Cristian I, Haynes D, DiTroia S, Meeks N, Delgado MR, Rosenfeld JA, Pais L, White SM, ... ... Wangler MF, et al. Germline mutation in : a heterogeneous, multi-systemic developmental disorder characterized by transcriptional dysregulation. Hgg Advances. 2. PMID 33665635 DOI: 10.1016/j.xhgg.2020.100014 |
0.355 |
|
| 2021 |
Khayat MM, Li H, Chander V, Hu J, Hansen AW, Li S, Traynelis J, Shen H, Weissenberger G, Stossi F, Johnson HL, Lupski JR, Posey JE, Sabo A, Meng Q, ... ... Wangler M, et al. Phenotypic and protein localization heterogeneity associated with AHDC1 pathogenic protein-truncating alleles in Xia-Gibbs Syndrome. Human Mutation. PMID 33644933 DOI: 10.1002/humu.24190 |
0.347 |
|
| 2021 |
Meng L, Isohanni P, Shao Y, Graham BH, Hickey SE, Brooks S, Suomalainen A, Joset P, Steindl K, Rauch A, Hackenberg A, High FA, Armstrong-Javors A, Mencacci NE, Gonzàlez-Latapi P, ... ... Wangler MF, et al. MED27 variansts cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia. Annals of Neurology. PMID 33443317 DOI: 10.1002/ana.26019 |
0.347 |
|
| 2020 |
Rossetti LZ, Bekheirnia MR, Lewis AM, Mefford HC, Golden-Grant K, Tarczy-Hornoch K, Briere LC, Sweetser DA, Walker MA, Kravets E, Stevenson DA, Bruenner G, Sebastian J, Knapo J, Rosenfeld JA, ... ... Wangler MF, et al. Missense variants in CTNNB1 can be associated with vitreoretinopathy-Seven new cases of CTNNB1-associated neurodevelopmental disorder including a previously unreported retinal phenotype. Molecular Genetics & Genomic Medicine. e1542. PMID 33350591 DOI: 10.1002/mgg3.1542 |
0.751 |
|
| 2020 |
Barish S, Barakat TS, Michel BC, Mashtalir N, Phillips JB, Valencia AM, Ugur B, Wegner J, Scott TM, Bostwick B, Murdock DR, Dai H, Perenthaler E, Nikoncuk A, ... ... Wangler M, et al. BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms. American Journal of Human Genetics. PMID 33232675 DOI: 10.1016/j.ajhg.2020.11.003 |
0.831 |
|
| 2020 |
Dutta D, Briere LC, Kanca O, Marcogliese PC, Walker MA, High FA, Vanderver A, Krier J, Carmichael N, Callahan C, Taft RJ, Simons C, Helman G, Network UD, Wangler MF, et al. De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment. Human Molecular Genetics. PMID 32356556 DOI: 10.1093/Hmg/Ddaa081 |
0.814 |
|
| 2020 |
Chung HL, Mao X, Wang H, Park YJ, Marcogliese PC, Rosenfeld JA, Burrage LC, Liu P, Murdock DR, Yamamoto S, Wangler MF, Chao HT, Long H, Feng L, et al. De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy. American Journal of Human Genetics. PMID 32330417 DOI: 10.1016/J.Ajhg.2020.04.001 |
0.835 |
|
| 2020 |
Chung HL, Wangler MF, Marcogliese PC, Jo J, Ravenscroft TA, Zuo Z, Duraine L, Sadeghzadeh S, Li-Kroeger D, Schmidt RE, Pestronk A, Rosenfeld JA, Burrage L, Herndon MJ, Chen S, et al. Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms. Neuron. PMID 32169171 DOI: 10.1016/J.Neuron.2020.02.021 |
0.773 |
|
| 2019 |
Graves HK, Jangam S, Tan KL, Pignata A, Seto ES, Yamamoto S, Wangler MF. A Genetic Screen for Genes That Impact Peroxisomes in Identifies Candidate Genes for Human Disease. G3 (Bethesda, Md.). PMID 31767637 DOI: 10.1534/G3.119.400803 |
0.687 |
|
| 2019 |
Hansen AW, Murugan M, Li H, Khayat MM, Wang L, Rosenfeld J, Andrews BK, Jhangiani SN, Coban Akdemir ZH, Sedlazeck FJ, Ashley-Koch AE, Liu P, Muzny DM, Davis EE, ... ... Wangler MF, et al. A Genocentric Approach to Discovery of Mendelian Disorders. American Journal of Human Genetics. PMID 31668702 DOI: 10.1016/J.Ajhg.2019.09.027 |
0.37 |
|
| 2019 |
Guo H, Bettella E, Marcogliese PC, Zhao R, Andrews JC, Nowakowski TJ, Gillentine MA, Hoekzema K, Wang T, Wu H, Jangam S, Liu C, Ni H, Willemsen MH, van Bon BW, ... ... Wangler MF, et al. Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders. Nature Communications. 10: 4679. PMID 31616000 DOI: 10.1038/S41467-019-12435-8 |
0.819 |
|
| 2019 |
Harnish JM, Deal SL, Chao HT, Wangler MF, Yamamoto S. In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila. Journal of Visualized Experiments : Jove. PMID 31498321 DOI: 10.3791/59658 |
0.693 |
|
| 2019 |
Kanca O, Andrews JC, Lee PT, Patel C, Braddock SR, Slavotinek AM, Cohen JS, Gubbels CS, Aldinger KA, Williams J, Indaram M, Fatemi A, Yu TW, Agrawal PB, Vezina G, ... ... Wangler MF, et al. De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia. American Journal of Human Genetics. 105: 672-674. PMID 31491411 DOI: 10.1016/J.Ajhg.2019.07.017 |
0.788 |
|
| 2019 |
Kanca O, Andrews JC, Lee PT, Patel C, Braddock SR, Slavotinek AM, Cohen JS, Gubbels CS, Aldinger KA, Williams J, Indaram M, Fatemi A, Yu TW, Agrawal PB, Vezina G, ... ... Wangler MF, et al. De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia. American Journal of Human Genetics. PMID 31327508 DOI: 10.1016/J.Ajhg.2019.06.014 |
0.842 |
|
| 2019 |
Bellen HJ, Wangler MF, Yamamoto S. The fruit fly at the interface of diagnosis and pathogenic mechanisms of rare and common human diseases. Human Molecular Genetics. PMID 31227826 DOI: 10.1093/Hmg/Ddz135 |
0.643 |
|
| 2018 |
Splinter K, Adams DR, Bacino CA, Bellen HJ, Bernstein JA, Cheatle-Jarvela AM, Eng CM, Esteves C, Gahl WA, Hamid R, Jacob HJ, Kikani B, Koeller DM, Kohane IS, Lee BH, ... ... Wangler MF, et al. Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease. The New England Journal of Medicine. PMID 30304647 DOI: 10.1056/Nejmoa1714458 |
0.546 |
|
| 2018 |
Marcogliese PC, Shashi V, Spillmann RC, Stong N, Rosenfeld JA, Koenig MK, Martínez-Agosto JA, Herzog M, Chen AH, Dickson PI, Lin HJ, Vera MU, Salamon N, Graham JM, Ortiz D, ... ... Wangler MF, et al. IRF2BPL Is Associated with Neurological Phenotypes. American Journal of Human Genetics. 103: 456. PMID 30193138 DOI: 10.1016/j.ajhg.2018.08.010 |
0.791 |
|
| 2018 |
Marcogliese PC, Shashi V, Spillmann RC, Stong N, Rosenfeld JA, Koenig MK, Martínez-Agosto JA, Herzog M, Chen AH, Dickson PI, Lin HJ, Vera MU, Salamon N, Ortiz D, Infante E, ... ... Wangler MF, et al. IRF2BPL Is Associated with Neurological Phenotypes. American Journal of Human Genetics. PMID 30057031 DOI: 10.1016/J.Ajhg.2018.07.006 |
0.833 |
|
| 2018 |
Snijders Blok L, Hiatt SM, Bowling KM, Prokop JW, Engel KL, Cochran JN, Bebin EM, Bijlsma EK, Ruivenkamp CAL, Terhal P, Simon MEH, Smith R, Hurst JA, McLaughlin H, ... ... Wangler MF, et al. De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder. Human Genetics. PMID 29740699 DOI: 10.1007/S00439-018-1887-Y |
0.365 |
|
| 2018 |
Liu N, Schoch K, Luo X, Pena L, Bhavana VH, Kukolich MK, Stringer S, Powis Z, Radtke K, Mroske C, Deak K, McDonald MT, McConkie-Rosell A, Markert ML, Kranz PG, ... ... Wangler MF, et al. Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder. Human Molecular Genetics. PMID 29726930 DOI: 10.1093/Hmg/Ddy146 |
0.67 |
|
| 2018 |
Jiang Y, Wangler MF, McGuire AL, Lupski JR, Posey JE, Khayat MM, Murdock DR, Sanchez-Pulido L, Ponting CP, Xia F, Hunter JV, Meng Q, Murugan M, Gibbs RA. The phenotypic spectrum of Xia-Gibbs syndrome. American Journal of Medical Genetics. Part A. PMID 29696776 DOI: 10.1002/Ajmg.A.38699 |
0.333 |
|
| 2018 |
Tan KL, Haelterman NA, Kwartler CS, Regalado ES, Lee PT, Nagarkar-Jaiswal S, Guo DC, Duraine L, Wangler MF, Bamshad MJ, Nickerson DA, Lin G, Milewicz DM, Bellen HJ. Ari-1 Regulates Myonuclear Organization Together with Parkin and Is Associated with Aortic Aneurysms. Developmental Cell. 45: 226-244.e8. PMID 29689197 DOI: 10.1016/J.Devcel.2018.03.020 |
0.8 |
|
| 2018 |
Wangler MF, Assia Batzir N, Robak LA, Koenig MK, Bacino CA, Scaglia F, Bellen HJ. The expanding neurological phenotype of DNM1L-related disorders. Brain : a Journal of Neurology. PMID 29529134 DOI: 10.1093/brain/awy024 |
0.474 |
|
| 2018 |
Oláhová M, Yoon WH, Thompson K, Jangam S, Fernandez L, Davidson JM, Kyle JE, Grove ME, Fisk DG, Kohler JN, Holmes M, Dries AM, Huang Y, Zhao C, Contrepois K, ... ... Wangler MF, et al. Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder. American Journal of Human Genetics. PMID 29478781 DOI: 10.1016/J.Ajhg.2018.01.020 |
0.589 |
|
| 2017 |
Wangler MF, Yamamoto S, Chao HT, Posey JE, Westerfield M, Postlethwait J, Hieter P, Boycott KM, Campeau PM, Bellen HJ. Model Organisms Facilitate Rare Disease Diagnosis and Therapeutic Research. Genetics. 207: 9-27. PMID 28874452 DOI: 10.1534/Genetics.117.203067 |
0.69 |
|
| 2017 |
Luo X, Rosenfeld JA, Yamamoto S, Harel T, Zuo Z, Hall M, Wierenga K, Pastore MT, Bartholomew D, Delgado MR, Rotenberg J, Lewis RA, Emrick L, Bacino CA, Eldomery MK, ... ... Wangler MF, et al. Clinically severe CACNA1A alleles affect synaptic function and neurodegeneration differentially. Plos Genetics. 13: e1006905. PMID 28742085 DOI: 10.1371/Journal.Pgen.1006905 |
0.684 |
|
| 2017 |
Wangler MF, Chao YH, Bayat V, Giagtzoglou N, Shinde AB, Putluri N, Coarfa C, Donti T, Graham BH, Faust JE, McNew JA, Moser A, Sardiello M, Baes M, Bellen HJ. Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouse. Plos Genetics. 13: e1006825. PMID 28640802 DOI: 10.1371/Journal.Pgen.1006825 |
0.801 |
|
| 2017 |
Halim D, Brosens E, Muller F, Wangler MF, Beaudet AL, Lupski JR, Akdemir ZHC, Doukas M, Stoop HJ, de Graaf BM, Brouwer RWW, van Ijcken WFJ, Oury JF, Rosenblatt J, Burns AJ, et al. Loss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis Syndrome. American Journal of Human Genetics. PMID 28602422 DOI: 10.1016/j.ajhg.2017.05.011 |
0.389 |
|
| 2017 |
Wang J, Al-Ouran R, Hu Y, Kim SY, Wan YW, Wangler MF, Yamamoto S, Chao HT, Comjean A, Mohr SE, Perrimon N, Liu Z, Bellen HJ. MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome. American Journal of Human Genetics. PMID 28502612 DOI: 10.1016/J.Ajhg.2017.04.010 |
0.77 |
|
| 2017 |
Wangler MF, Hu Y, Shulman JM. Drosophila and genome-wide association studies: a review and resource for the functional dissection of human complex traits. Disease Models & Mechanisms. 10: 77-88. PMID 28151408 DOI: 10.1242/Dmm.027680 |
0.351 |
|
| 2017 |
Schoch K, Meng L, Szelinger S, Bearden DR, Stray-Pedersen A, Busk OL, Stong N, Liston E, Cohn RD, Scaglia F, Rosenfeld JA, Tarpinian J, Skraban CM, Deardorff MA, Friedman JN, ... ... Wangler MF, et al. A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay. American Journal of Human Genetics. PMID 28132692 DOI: 10.1016/J.Ajhg.2016.12.013 |
0.442 |
|
| 2016 |
Yoon WH, Sandoval H, Nagarkar-Jaiswal S, Jaiswal M, Yamamoto S, Haelterman NA, Putluri N, Putluri V, Sreekumar A, Tos T, Aksoy A, Donti T, Graham BH, Ohno M, Nishi E, ... ... Wangler MF, et al. Loss of Nardilysin, a Mitochondrial Co-chaperone for α-Ketoglutarate Dehydrogenase, Promotes mTORC1 Activation and Neurodegeneration. Neuron. PMID 28017472 DOI: 10.1016/J.Neuron.2016.11.038 |
0.78 |
|
| 2016 |
Chao HT, Davids M, Burke E, Pappas JG, Rosenfeld JA, McCarty AJ, Davis T, Wolfe L, Toro C, Tifft C, Xia F, Stong N, Johnson TK, Warr CG, ... ... Wangler MF, et al. A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3. American Journal of Human Genetics. PMID 28017372 DOI: 10.1016/J.Ajhg.2016.11.018 |
0.755 |
|
| 2016 |
Chao YH, Robak LA, Xia F, Koenig MK, Adesina A, Bacino CA, Scaglia F, Bellen HJ, Wangler MF. Missense variants in the middle domain of DNM1L in cases of infantile encephalopathy alter peroxisomes and mitochondria when assayed in Drosophila. Human Molecular Genetics. PMID 26931468 DOI: 10.1093/Hmg/Ddw059 |
0.559 |
|
| 2016 |
Bacino C, Chao YH, Seto E, Lotze T, Xia F, Jones RO, Moser A, Wangler MF. Dataset for a case report of a homozygous PEX16 F332del mutation. Data in Brief. 6: 722-7. PMID 26870756 DOI: 10.1016/j.dib.2015.12.011 |
0.569 |
|
| 2015 |
Bacino C, Chao YH, Seto E, Lotze T, Xia F, Jones RO, Moser A, Wangler MF. A homozygous mutation in PEX16 identified by whole-exome sequencing ending a diagnostic odyssey. Molecular Genetics and Metabolism Reports. 5: 15-18. PMID 26644994 DOI: 10.1016/j.ymgmr.2015.09.001 |
0.549 |
|
| 2015 |
Wangler M, Bayat V, Bellen H. A Mitochondrial Translation Defect Identified by Whole-Exome Sequencing Expands the Phenotypic Spectrum for MARS2. Human Mutation. 36: iii. PMID 25989390 DOI: 10.1002/Humu.22811 |
0.776 |
|
| 2015 |
Wangler MF, Yamamoto S, Bellen HJ. Fruit flies in biomedical research. Genetics. 199: 639-53. PMID 25624315 DOI: 10.1534/Genetics.114.171785 |
0.551 |
|
| 2014 |
Yamamoto S, Jaiswal M, Charng WL, Gambin T, Karaca E, Mirzaa G, Wiszniewski W, Sandoval H, Haelterman NA, Xiong B, Zhang K, Bayat V, David G, Li T, Chen K, ... ... Wangler MF, et al. A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases. Cell. 159: 200-14. PMID 25259927 DOI: 10.1016/J.Cell.2014.09.002 |
0.783 |
|
| 2014 |
Faust JE, Manisundaram A, Ivanova PT, Milne SB, Summerville JB, Brown HA, Wangler M, Stern M, McNew JA. Peroxisomes are required for lipid metabolism and muscle function in Drosophila melanogaster. Plos One. 9: e100213. PMID 24945818 DOI: 10.1371/Journal.Pone.0100213 |
0.375 |
|
| 2014 |
Xia F, Bainbridge MN, Tan TY, Wangler MF, Scheuerle AE, Zackai EH, Harr MH, Sutton VR, Nalam RL, Zhu W, Nash M, Ryan MM, Yaplito-Lee J, Hunter JV, Deardorff MA, et al. De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea. American Journal of Human Genetics. 94: 784-9. PMID 24791903 DOI: 10.1016/J.Ajhg.2014.04.006 |
0.342 |
|
| 2014 |
Wangler MF, Gonzaga-Jauregui C, Gambin T, Penney S, Moss T, Chopra A, Probst FJ, Xia F, Yang Y, Werlin S, Eglite I, Kornejeva L, Bacino CA, Baldridge D, Neul J, et al. Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndrome. Plos Genetics. 10: e1004258. PMID 24676022 DOI: 10.1371/Journal.Pgen.1004258 |
0.311 |
|
| 2011 |
Wangler MF, Reiter LT, Zimm G, Trimble-Morgan J, Wu J, Bier E. Antioxidant proteins TSA and PAG interact synergistically with Presenilin to modulate Notch signaling in Drosophila. Protein & Cell. 2: 554-63. PMID 21822800 DOI: 10.1007/S13238-011-1073-7 |
0.317 |
|
| 2005 |
Chang AS, Moley KH, Wangler M, Feinberg AP, Debaun MR. Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients. Fertility and Sterility. 83: 349-54. PMID 15705373 DOI: 10.1016/J.Fertnstert.2004.07.964 |
0.342 |
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| Low-probability matches (unlikely to be authored by this person) |
| 2019 |
Murdock DR, Jiang Y, Wangler M, Khayat MM, Sabo A, Juusola J, McWalter K, Schatz KS, Gunay-Aygun M, Gibbs RA. Xia-Gibbs Syndrome in adulthood: a case report with insight into the natural history of the condition. Cold Spring Harbor Molecular Case Studies. PMID 30622101 DOI: 10.1101/mcs.a003608 |
0.293 |
|
| 2019 |
Assia Batzir N, Bhagwat P, Eble T, Liu P, Eng C, Elsea SH, Robak LA, Scaglia F, Goldman A, Dhar SU, Wangler MF. De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizures. Cold Spring Harbor Molecular Case Studies. PMID 30850373 DOI: 10.1101/mcs.a003673 |
0.293 |
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| 2019 |
Assia Batzir N, Kishor Bhagwat P, Larson A, Coban Akdemir Z, Bagłaj M, Bofferding L, Bosanko KB, Bouassida S, Callewaert B, Cannon A, Enchautegui Colon Y, Garnica AD, Harr MH, Heck S, Hurst AC, ... ... Wangler MF, et al. Recurrent Arginine Substitutions in the ACTG2 Gene are the Primary Driver of Disease Burden and Severity in Visceral Myopathy. Human Mutation. PMID 31769566 DOI: 10.1002/Humu.23960 |
0.285 |
|
| 2015 |
Braverman NE, Raymond GV, Rizzo WB, Moser AB, Wilkinson ME, Stone EM, Steinberg SJ, Wangler MF, Rush ET, Hacia JG, Bose M. Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines. Molecular Genetics and Metabolism. PMID 26750748 DOI: 10.1016/J.Ymgme.2015.12.009 |
0.279 |
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| 2020 |
Liu J, Ding G, Zou K, Jiang Z, Zhang J, Lu Y, Pignata A, Venner E, Liu P, Liu Z, Wangler MF, Sun Z. Genome sequencing analysis of a family with a child displaying severe abdominal distention and recurrent hypoglycemia. Molecular Genetics & Genomic Medicine. e1130. PMID 31971667 DOI: 10.1002/Mgg3.1130 |
0.274 |
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| 2024 |
German RJ, Vuocolo B, Vossaert L, Owen N, Lewis RA, Saba L, Wangler MF, Nagamani S. Novel hemizygous single-nucleotide duplication in RPGR in a patient with retinal dystrophy and sensorineural hearing loss. Molecular Genetics & Genomic Medicine. 12: e2404. PMID 38404254 DOI: 10.1002/mgg3.2404 |
0.269 |
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| 2016 |
Ventura MJ, Wheaton D, Xu M, Birch D, Bowne SJ, Sullivan LS, Daiger SP, Whitney AE, Jones RO, Moser AB, Chen R, Wangler MF. Diagnosis of a mild peroxisomal phenotype with next-generation sequencing. Molecular Genetics and Metabolism Reports. 9: 75-78. PMID 27872819 DOI: 10.1016/J.Ymgmr.2016.10.006 |
0.266 |
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| 2011 |
Fruhman G, Landsverk ML, Lotze TE, Hunter JV, Wangler MF, Adesina AM, Wong LJ, Scaglia F. Atypical presentation of Leigh syndrome associated with a Leber hereditary optic neuropathy primary mitochondrial DNA mutation. Molecular Genetics and Metabolism. 103: 153-60. PMID 21414825 DOI: 10.1016/J.Ymgme.2011.02.014 |
0.265 |
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| 2022 |
Lyons-Warren AM, Wangler MF, Wan YW. Cluster Analysis of Short Sensory Profile Data Reveals Sensory-Based Subgroups in Autism Spectrum Disorder. International Journal of Molecular Sciences. 23. PMID 36361815 DOI: 10.3390/ijms232113030 |
0.256 |
|
| 2009 |
Defranco E, Shen T, Wangler M, Kistka Z, Palomar L, Stormo A, Plunkett J, Huettner P, Muglia L. 498: Placental pathology findings in cases of familial spontaneous preterm birth American Journal of Obstetrics and Gynecology. 201: S186. DOI: 10.1016/J.Ajog.2009.10.664 |
0.243 |
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| 2018 |
Bellettato CM, Hubert L, Scarpa M, Wangler MF. Inborn Errors of Metabolism Involving Complex Molecules: Lysosomal and Peroxisomal Storage Diseases. Pediatric Clinics of North America. 65: 353-373. PMID 29502918 DOI: 10.1016/j.pcl.2017.11.011 |
0.241 |
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| 2016 |
Donti TR, Cappuccio G, Hubert L, Neira J, Atwal PS, Miller MJ, Cardon AL, Sutton VR, Porter BE, Baumer FM, Wangler MF, Sun Q, Emrick LT, Elsea SH. Diagnosis of adenylosuccinate lyase deficiency by metabolomic profiling in plasma reveals a phenotypic spectrum. Molecular Genetics and Metabolism Reports. 8: 61-6. PMID 27504266 DOI: 10.1016/J.Ymgmr.2016.07.007 |
0.24 |
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| 2018 |
Koczkowska M, Callens T, Gomes A, Sharp A, Chen Y, Hicks AD, Aylsworth AS, Azizi AA, Basel DG, Bellus G, Bird LM, Blazo MA, Burke LW, Cannon A, Collins F, ... ... Wangler MF, et al. Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlation. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30275510 DOI: 10.1038/S41436-018-0326-8 |
0.238 |
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| 2018 |
Koczkowska M, Callens T, Gomes A, Sharp A, Chen Y, Hicks AD, Aylsworth AS, Azizi AA, Basel DG, Bellus G, Bird LM, Blazo MA, Burke LW, Cannon A, Collins F, ... ... Wangler MF, et al. Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlation. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30190611 DOI: 10.1038/S41436-018-0269-0 |
0.235 |
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| 2005 |
Wangler MF, An P, Feinberg AP, Province M, Debaun MR. Inheritance pattern of Beckwith-Wiedemann syndrome is heterogeneous in 291 families with an affected proband. American Journal of Medical Genetics. Part A. 137: 16-21. PMID 16007611 DOI: 10.1002/Ajmg.A.30827 |
0.226 |
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| 2022 |
Grosso BJ, Kramer AA, Tyagi S, Bennett DF, Tifft CJ, D'Souza P, Wangler MF, Macnamara EF, Meza U, Bannister RA. Complex effects on Ca2.1 channel gating caused by a CACNA1A variant associated with a severe neurodevelopmental disorder. Scientific Reports. 12: 9186. PMID 35655070 DOI: 10.1038/s41598-022-12789-y |
0.221 |
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| 2010 |
Tompson SW, Bacino CA, Safina NP, Bober MB, Proud VK, Funari T, Wangler MF, Nevarez L, Ala-Kokko L, Wilcox WR, Eyre DR, Krakow D, Cohn DH. Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen gene. American Journal of Human Genetics. 87: 708-12. PMID 21035103 DOI: 10.1016/j.ajhg.2010.10.009 |
0.218 |
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| 2020 |
Schulze KV, Hanchard NA, Wangler MF. Biases in arginine codon usage correlate with genetic disease risk. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 22: 1407-1412. PMID 32371920 DOI: 10.1038/s41436-020-0813-6 |
0.203 |
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| 2017 |
Meng L, Pammi M, Saronwala A, Magoulas P, Ghazi AR, Vetrini F, Zhang J, He W, Dharmadhikari AV, Qu C, Ward P, Braxton A, Narayanan S, Ge X, Tokita MJ, ... ... Wangler MF, et al. Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management. Jama Pediatrics. e173438. PMID 28973083 DOI: 10.1001/Jamapediatrics.2017.3438 |
0.202 |
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| 2019 |
Koczkowska M, Callens T, Chen Y, Gomes A, Hicks AD, Sharp A, Johns E, Uhas KA, Armstrong L, Bosanko KA, Babovic-Vuksanovic D, Baker L, Basel DG, Bengala M, Bennett JT, ... ... Wangler MF, et al. Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276 and p.Lys1423: genotype-phenotype study in neurofibromatosis type 1. Human Mutation. PMID 31595648 DOI: 10.1002/Humu.23929 |
0.198 |
|
| 2017 |
Eldomery MK, Coban-Akdemir Z, Harel T, Rosenfeld JA, Gambin T, Stray-Pedersen A, Küry S, Mercier S, Lessel D, Denecke J, Wiszniewski W, Penney S, Liu P, Bi W, Lalani SR, ... ... Wangler MF, et al. Lessons learned from additional research analyses of unsolved clinical exome cases. Genome Medicine. 9: 26. PMID 28327206 DOI: 10.1186/S13073-017-0412-6 |
0.189 |
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| 2013 |
Wangler MF, Chavan R, Hicks MJ, Nuchtern JG, Hegde M, Plon SE, Thompson PA. Unusually early presentation of small-bowel adenocarcinoma in a patient with Peutz-Jeghers syndrome. Journal of Pediatric Hematology/Oncology. 35: 323-8. PMID 23426006 DOI: 10.1097/Mph.0B013E318282Db11 |
0.186 |
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| 2020 |
Martinez-Moreno R, Selga E, Riuró H, Carreras D, Parnes M, Srinivasan C, Wangler MF, Pérez GJ, Scornik FS, Brugada R. An Variant Affects Both Cardiac-Type (Na1.5) and Brain-Type (Na1.1) Sodium Currents and Contributes to Complex Concomitant Brain and Cardiac Disorders. Frontiers in Cell and Developmental Biology. 8: 528742. PMID 33134290 DOI: 10.3389/fcell.2020.528742 |
0.183 |
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| 2018 |
Wangler MF, Hubert L, Donti TR, Ventura MJ, Miller MJ, Braverman N, Gawron K, Bose M, Moser AB, Jones RO, Rizzo WB, Sutton VR, Sun Q, Kennedy AD, Elsea SH. A metabolomic map of Zellweger spectrum disorders reveals novel disease biomarkers. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29419819 DOI: 10.1038/Gim.2017.262 |
0.183 |
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| 2023 |
Wangler MF, Lesko B, Dahal R, Jangam S, Bhadane P, Wilson TE, McPheron M, Miller MJ. Dicarboxylic acylcarnitine biomarkers in peroxisome biogenesis disorders. Molecular Genetics and Metabolism. 140: 107680. PMID 37567036 DOI: 10.1016/j.ymgme.2023.107680 |
0.182 |
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| 2022 |
Thistlethwaite LR, Li X, Burrage LC, Riehle K, Hacia JG, Braverman N, Wangler MF, Miller MJ, Elsea SH, Milosavljevic A. Clinical diagnosis of metabolic disorders using untargeted metabolomic profiling and disease-specific networks learned from profiling data. Scientific Reports. 12: 6556. PMID 35449147 DOI: 10.1038/s41598-022-10415-5 |
0.181 |
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| 2009 |
Plunkett J, Feitosa MF, Trusgnich M, Wangler MF, Palomar L, Kistka ZA, DeFranco EA, Shen TT, Stormo AE, Puttonen H, Hallman M, Haataja R, Luukkonen A, Fellman V, Peltonen L, et al. Mother's genome or maternally-inherited genes acting in the fetus influence gestational age in familial preterm birth. Human Heredity. 68: 209-19. PMID 19521103 DOI: 10.1159/000224641 |
0.157 |
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| 2023 |
Ford CP, Littlejohn RO, German R, Vuocolo B, Aceves J, Vossaert L, Owen N, Wangler M, Schmid CA. Precision therapy for a medically actionable ATP1A3 variant from a genomic medicine program in an underserved population. Molecular Genetics & Genomic Medicine. e2272. PMID 37614148 DOI: 10.1002/mgg3.2272 |
0.153 |
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| 2019 |
Sze SK, Lederman HM, Crawford TO, Wangler MF, Lewis AM, Kastan MB, Dibra HK, Taylor AMR, Wechsler DS. Retrospective Diagnosis of Ataxia-Telangiectasia in an Adolescent Patient With a Remote History of T-Cell Leukemia. Journal of Pediatric Hematology/Oncology. PMID 31743320 DOI: 10.1097/MPH.0000000000001672 |
0.132 |
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| 2005 |
Wangler MF, Chang AS, Moley KH, Feinberg AP, Debaun MR. Factors associated with preterm delivery in mothers of children with Beckwith-Wiedemann syndrome: a case cohort study from the BWS registry. American Journal of Medical Genetics. Part A. 134: 187-91. PMID 15723285 DOI: 10.1002/Ajmg.A.30595 |
0.071 |
|
| 2007 |
Kistka ZA, Palomar L, Lee KA, Boslaugh SE, Wangler MF, Cole FS, DeBaun MR, Muglia LJ. Racial disparity in the frequency of recurrence of preterm birth. American Journal of Obstetrics and Gynecology. 196: 131.e1-6. PMID 17306652 DOI: 10.1016/j.ajog.2006.06.093 |
0.063 |
|
| 1980 |
Drenckhahn W, Feigel A, Finckh E, Gademann G, Rüskamp K, Wangler M, Zemło L. Investigation of the Sn(p, p0) and (p, n) reaction at sub-coulomb energies Nuclear Physics, Section A. 339: 13-22. DOI: 10.1016/0375-9474(80)90238-9 |
0.047 |
|
| 2002 |
Wangler M, Roth DA, Krivtsun VM, Pak I, Winnewisser G, Geleijns M, Wormer PE, van der Avoird A. High resolution TDL spectroscopy of the Ar-CH4 complex. Spectrochimica Acta. Part a, Molecular and Biomolecular Spectroscopy. 58: 2499-504. PMID 12353700 DOI: 10.1016/S1386-1425(02)00067-7 |
0.043 |
|
| 2007 |
Schumacher M, Wangler M, Wolkewitz M, Beyersmann J. Attributable mortality due to nosocomial infections: A simple and useful application of multistate models Methods of Information in Medicine. 46: 595-600. PMID 17938785 DOI: 10.1160/ME9062 |
0.037 |
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| 2019 |
Carrasco D, Magoulas P, Scull JC, Jarrell JA, Lalani SR, Wangler MF. Digital necrosis in an infant with severe spinal muscular atrophy. Neurology. Genetics. 5: e361. PMID 31742229 DOI: 10.1212/NXG.0000000000000361 |
0.034 |
|
| 1978 |
Kretschmer W, Wangler M. Model-independent determination of the compound-elastic enhancement factor in a polarized-proton fluctuation experiment Physical Review Letters. 41: 1224-1226. DOI: 10.1103/PhysRevLett.41.1224 |
0.034 |
|
| 2003 |
Wangler M, Roth DA, Pak I, Winnewisser G, Wormer PES, Van der Avoird A. The high-resolution spectrum of the Ar-CH4 complex in the 7 μm region: Measurement and ab initio calculation Journal of Molecular Spectroscopy. 222: 109-120. DOI: 10.1016/S0022-2852(03)00058-4 |
0.033 |
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| 2011 |
Wangler M, Fujikawa R, Hestbæk L, Michielsen T, Raven TJ, Thiel HW, Zaugg B. Creating European guidelines for Chiropractic Incident Reporting and Learning Systems (CIRLS): Relevance and structure Chiropractic and Manual Therapies. 19. DOI: 10.1186/2045-709X-19-9 |
0.025 |
|
| 1997 |
Wangler MD, Thapar P, Skerman JH. Decreased mivacurium constant infusion requirements with defasciculating doses of pancuronium Anesthesia and Analgesia. 84: 668-671. PMID 9052321 DOI: 10.1097/00000539-199703000-00037 |
0.023 |
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| 2013 |
Wangler M, Peterson C, Zaugg B, Thiel H, Finch R. How do chiropractors manage clinical risk? A questionnaire study Chiropractic and Manual Therapies. 21. DOI: 10.1186/2045-709X-21-18 |
0.023 |
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| 2005 |
Petkov MP, Napolitano CA, Tobler HG, Ferrer TJ, Palacios JM, Wangler MD. A rupture of both atrioventricular valves after blunt chest trauma: the usefulness of transesophageal echocardiography for a life-saving diagnosis. Anesthesia and Analgesia. 100: 1256-8, table of con. PMID 15845663 DOI: 10.1213/01.ANE.0000149543.15866.80 |
0.022 |
|
| 1997 |
Oras JJ, Towell RH, Wangler ME. Leakage test concerns for packagings with three-O-ring closure seals American Society of Mechanical Engineers, Pressure Vessels and Piping Division (Publication) Pvp. 348: 97-99. |
0.018 |
|
| 1983 |
Wangler MA, Rosenblatt RM, Gourlay GK. Methadone titration to avoid excessive respiratory depression Anesthesiology. 59: 363-364. PMID 6614552 |
0.015 |
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| 1983 |
Wangler MA, Gupta B. Preferred treatment of fentanyl-induced postoperative rigidity Anesthesiology. 59: 594. PMID 6650923 |
0.011 |
|
| 2010 |
Wangler M, Zaugg B, Faigaux E. Medication Prescription: A Pilot Survey of Bernese Doctors of Chiropractic Practicing in Switzerland Journal of Manipulative and Physiological Therapeutics. 33: 231-237. PMID 20350678 DOI: 10.1016/j.jmpt.2010.01.013 |
0.01 |
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| 2009 |
Zaugg B, Wangler M. A Model Framework for Patient Safety Training in Chiropractic: A Literature Synthesis Journal of Manipulative and Physiological Therapeutics. 32: 493-499. PMID 19712793 DOI: 10.1016/j.jmpt.2009.06.004 |
0.01 |
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| 2003 |
Hafner RS, Hensel SJ, Bebak RB, Smith AC, Wangler ME. American Society of Mechanical Engineers, Pressure Vessels and Piping Division (Publication) PVP: Forword American Society of Mechanical Engineers, Pressure Vessels and Piping Division (Publication) Pvp. 467: iii. |
0.01 |
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| 2001 |
Wangler M, Roth DA, Winnewisser G, Pak I, McKellar ARW. Diode laser spectroscopy of the weakly bound complex Ne-CH4 Canadian Journal of Physics. 79: 423-434. DOI: 10.1139/cjp-79-2-3-423 |
0.01 |
|
| 1985 |
Wangler MA, Kilpatrick DS. Aminophylline is an antagonist of lorazepam Anesthesia and Analgesia. 64: 834-836. PMID 4014747 |
0.01 |
|
| 1985 |
Wangler MA, Craner DE. Another method to provide left uterine displacement Anesthesiology. 62: 700-701. PMID 3994050 |
0.01 |
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| 1984 |
Wangler MA, Weaver JM. A method to facilitate fiberoptic laryngoscopy Anesthesiology. 61: 111. PMID 6742474 |
0.01 |
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| 1982 |
Zemło L, Drenckhahn W, Feigel A, Finckh E, Rüskamp K, Urbainsky P, Wangler M. The 209Bi(d,γ)211,211mPo reaction Nuclear Physics, Section A. 380: 493-501. DOI: 10.1016/0375-9474(82)90573-5 |
0.01 |
|
| 1980 |
Kleine N, Fetta F, Wangler M. Positive effect of inosine on the antibody system | POSITIVER EFFEKT VON INOSIN AUF DIE ANTIKORPERANTWORT Therapiewoche. 30: 2463-2466. |
0.01 |
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| Hide low-probability matches. |