Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 136

1.

Prominence of Pairing in Inclusive (p,2p) and (p,pn) Cross Sections from Neutron-Rich Nuclei.

Paul N, Obertelli A, Bertulani CA, Corsi A, Doornenbal P, Rodriguez-Sanchez JL, Authelet G, Baba H, Calvet D, Château F, Chen S, Delbart A, Gheller JM, Giganon A, Gillibert A, Isobe T, Lapoux V, Matsushita M, Momiyama S, Motobayashi T, Niikura M, Otsu H, Péron C, Peyaud A, Pollacco EC, Roussé JY, Sakurai H, Santamaria C, Sasano M, Shiga Y, Steppenbeck D, Takeuchi S, Taniuchi R, Uesaka T, Wang H, Yoneda K, Ando T, Arici T, Blazhev A, Browne F, Bruce AM, Carroll R, Chung LX, Cortés ML, Dewald M, Ding B, Dombradi Z, Flavigny F, Franchoo S, Giacoppo F, Górska M, Gottardo A, Hadynska-Klek K, Korkulu Z, Koyama S, Kubota Y, Jungclaus A, Lee J, Lettmann M, Linh BD, Liu J, Liu Z, Lizarazo C, Louchart C, Lozeva R, Matsui K, Miyazaki T, Moschner K, Nagamine S, Nakatsuka N, Nita C, Nishimura S, Nobs CR, Olivier L, Ota S, Patel Z, Podolyák Z, Rudigier M, Sahin E, Saito TY, Shand C, Söderström PA, Stefan IG, Sumikama T, Suzuki D, Orlandi R, Vaquero V, Vajta Z, Werner V, Wimmer K, Wu J, Xu Z.

Phys Rev Lett. 2019 Apr 26;122(16):162503. doi: 10.1103/PhysRevLett.122.162503.

PMID:
31075035
2.

Patients with High-Grade Gliomas and Café-au-Lait Macules: Is Neurofibromatosis Type 1 the Only Diagnosis?

Guerrini-Rousseau L, Suerink M, Grill J, Legius E, Wimmer K, Brugières L.

AJNR Am J Neuroradiol. 2019 May 9. doi: 10.3174/ajnr.A6058. [Epub ahead of print] No abstract available.

PMID:
31072978
3.

Neural mechanisms of vibrotactile categorization.

Malone PS, Eberhardt SP, Wimmer K, Sprouse C, Klein R, Glomb K, Scholl CA, Bokeria L, Cho P, Deco G, Jiang X, Bernstein LE, Riesenhuber M.

Hum Brain Mapp. 2019 Mar 28. doi: 10.1002/hbm.24581. [Epub ahead of print]

PMID:
30920706
4.

How Robust is the N=34 Subshell Closure? First Spectroscopy of ^{52}Ar.

Liu HN, Obertelli A, Doornenbal P, Bertulani CA, Hagen G, Holt JD, Jansen GR, Morris TD, Schwenk A, Stroberg R, Achouri N, Baba H, Browne F, Calvet D, Château F, Chen S, Chiga N, Corsi A, Cortés ML, Delbart A, Gheller JM, Giganon A, Gillibert A, Hilaire C, Isobe T, Kobayashi T, Kubota Y, Lapoux V, Motobayashi T, Murray I, Otsu H, Panin V, Paul N, Rodriguez W, Sakurai H, Sasano M, Steppenbeck D, Stuhl L, Sun YL, Togano Y, Uesaka T, Wimmer K, Yoneda K, Aktas O, Aumann T, Chung LX, Flavigny F, Franchoo S, Gašparić I, Gerst RB, Gibelin J, Hahn KI, Kim D, Koiwai T, Kondo Y, Koseoglou P, Lee J, Lehr C, Linh BD, Lokotko T, MacCormick M, Moschner K, Nakamura T, Park SY, Rossi D, Sahin E, Sohler D, Söderström PA, Takeuchi S, Törnqvist H, Vaquero V, Wagner V, Wang S, Werner V, Xu X, Yamada H, Yan D, Yang Z, Yasuda M, Zanetti L.

Phys Rev Lett. 2019 Feb 22;122(7):072502. doi: 10.1103/PhysRevLett.122.072502.

PMID:
30848641
5.

First Spectroscopy of the Near Drip-line Nucleus ^{40}Mg.

Crawford HL, Fallon P, Macchiavelli AO, Doornenbal P, Aoi N, Browne F, Campbell CM, Chen S, Clark RM, Cortés ML, Cromaz M, Ideguchi E, Jones MD, Kanungo R, MacCormick M, Momiyama S, Murray I, Niikura M, Paschalis S, Petri M, Sakurai H, Salathe M, Schrock P, Steppenbeck D, Takeuchi S, Tanaka YK, Taniuchi R, Wang H, Wimmer K.

Phys Rev Lett. 2019 Feb 8;122(5):052501. doi: 10.1103/PhysRevLett.122.052501.

PMID:
30822018
6.

A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes.

Gallon R, Mühlegger B, Wenzel SS, Sheth H, Hayes C, Aretz S, Dahan K, Foulkes W, Kratz CP, Ripperger T, Azizi AA, Baris Feldman H, Chong AL, Demirsoy U, Florkin B, Imschweiler T, Januszkiewicz-Lewandowska D, Lobitz S, Nathrath M, Pander HJ, Perez-Alonso V, Perne C, Ragab I, Rosenbaum T, Rueda D, Seidel MG, Suerink M, Taeubner J, Zimmermann SY, Zschocke J, Borthwick GM, Burn J, Jackson MS, Santibanez-Koref M, Wimmer K.

Hum Mutat. 2019 May;40(5):649-655. doi: 10.1002/humu.23721. Epub 2019 Mar 6.

PMID:
30740824
7.

Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy.

Suerink M, Ripperger T, Messiaen L, Menko FH, Bourdeaut F, Colas C, Jongmans M, Goldberg Y, Nielsen M, Muleris M, van Kouwen M, Slavc I, Kratz C, Vasen HF, Brugiѐres L, Legius E, Wimmer K.

J Med Genet. 2019 Feb;56(2):53-62. doi: 10.1136/jmedgenet-2018-105664. Epub 2018 Nov 10.

PMID:
30415209
8.

Cleft lip/palate and hereditary diffuse gastric cancer: report of a family harboring a CDH1 c.687 + 1G > A germline mutation and review of the literature.

Obermair F, Rammer M, Burghofer J, Malli T, Schossig A, Wimmer K, Kranewitter W, Mayrbaeurl B, Duba HC, Webersinke G.

Fam Cancer. 2019 Apr;18(2):253-260. doi: 10.1007/s10689-018-0111-5.

PMID:
30306390
9.

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.

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, DeFilippo C, Denayer E, Digilio MC, Dills SK, Dosa L, Greenwood RS, Griffis C, Gupta P, Hachen RK, Hernández-Chico C, Janssens S, Jones KJ, Jordan JT, Kannu P, Korf BR, Lewis AM, Listernick RH, Lonardo F, Mahoney MJ, Ojeda MM, McDonald MT, McDougall C, Mendelsohn N, Miller DT, Mori M, Oostenbrink R, Perreault S, Pierpont ME, Piscopo C, Pond DA, Randolph LM, Rauen KA, Rednam S, Rutledge SL, Saletti V, Schaefer GB, Schorry EK, Scott DA, Shugar A, Siqveland E, Starr LJ, Syed A, Trapane PL, Ullrich NJ, Wakefield EG, Walsh LE, Wangler MF, Zackai E, Claes KBM, Wimmer K, van Minkelen R, De Luca A, Martin Y, Legius E, Messiaen LM.

Genet Med. 2019 Mar;21(3):764-765. doi: 10.1038/s41436-018-0326-8.

PMID:
30275510
10.

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.

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, DeFilippo C, Denayer E, Digilio MC, Dills SK, Dosa L, Greenwood RS, Griffis C, Gupta P, Hachen RK, Hernández-Chico C, Janssens S, Jones KJ, Jordan JT, Kannu P, Korf BR, Lewis AM, Listernick RH, Lonardo F, Mahoney MJ, Ojeda MM, McDonald MT, McDougall C, Mendelsohn N, Miller DT, Mori M, Oostenbrink R, Perreault S, Pierpont ME, Piscopo C, Pond DA, Randolph LM, Rauen KA, Rednam S, Rutledge SL, Saletti V, Schaefer GB, Schorry EK, Scott DA, Shugar A, Siqveland E, Starr LJ, Syed A, Trapane PL, Ullrich NJ, Wakefield EG, Walsh LE, Wangler MF, Zackai E, Claes KBM, Wimmer K, van Minkelen R, De Luca A, Martin Y, Legius E, Messiaen LM.

Genet Med. 2019 Apr;21(4):867-876. doi: 10.1038/s41436-018-0269-0. Epub 2018 Sep 7. Erratum in: Genet Med. 2019 Mar;21(3):764-765.

PMID:
30190611
11.

No Overt Clinical Immunodeficiency Despite Immune Biological Abnormalities in Patients With Constitutional Mismatch Repair Deficiency.

Tesch VK, IJspeert H, Raicht A, Rueda D, Dominguez-Pinilla N, Allende LM, Colas C, Rosenbaum T, Ilencikova D, Baris HN, Nathrath MHM, Suerink M, Januszkiewicz-Lewandowska D, Ragab I, Azizi AA, Wenzel SS, Zschocke J, Schwinger W, Kloor M, Blattmann C, Brugieres L, van der Burg M, Wimmer K, Seidel MG.

Front Immunol. 2018 Jul 2;9:1506. doi: 10.3389/fimmu.2018.01506. eCollection 2018.

12.

Adjuvant Bisphosphonate Therapy in Postmenopausal Breast Cancer.

Strobl S, Wimmer K, Exner R, Devyatko Y, Bolliger M, Fitzal F, Gnant M.

Curr Treat Options Oncol. 2018 Mar 12;19(4):18. doi: 10.1007/s11864-018-0535-z. Review.

PMID:
29527635
13.

Optimal duration of adjuvant endocrine therapy: how to apply the newest data.

Wimmer K, Strobl S, Bolliger M, Devyatko Y, Korkmaz B, Exner R, Fitzal F, Gnant M.

Ther Adv Med Oncol. 2017 Nov;9(11):679-692. doi: 10.1177/1758834017732966. Epub 2017 Oct 27. Review.

14.

Diagnostic challenges in a child with early onset desmoplastic medulloblastoma and homozygous variants in MSH2 and MSH6.

Taeubner J, Wimmer K, Muleris M, Lascols O, Colas C, Fauth C, Brozou T, Felsberg J, Riemer J, Gombert M, Ginzel S, Hoell JI, Borkhardt A, Kuhlen M.

Eur J Hum Genet. 2018 Mar;26(3):440-444. doi: 10.1038/s41431-017-0071-5. Epub 2018 Jan 4.

15.

Comprehensive Analysis of Hypermutation in Human Cancer.

Campbell BB, Light N, Fabrizio D, Zatzman M, Fuligni F, de Borja R, Davidson S, Edwards M, Elvin JA, Hodel KP, Zahurancik WJ, Suo Z, Lipman T, Wimmer K, Kratz CP, Bowers DC, Laetsch TW, Dunn GP, Johanns TM, Grimmer MR, Smirnov IV, Larouche V, Samuel D, Bronsema A, Osborn M, Stearns D, Raman P, Cole KA, Storm PB, Yalon M, Opocher E, Mason G, Thomas GA, Sabel M, George B, Ziegler DS, Lindhorst S, Issai VM, Constantini S, Toledano H, Elhasid R, Farah R, Dvir R, Dirks P, Huang A, Galati MA, Chung J, Ramaswamy V, Irwin MS, Aronson M, Durno C, Taylor MD, Rechavi G, Maris JM, Bouffet E, Hawkins C, Costello JF, Meyn MS, Pursell ZF, Malkin D, Tabori U, Shlien A.

Cell. 2017 Nov 16;171(5):1042-1056.e10. doi: 10.1016/j.cell.2017.09.048. Epub 2017 Oct 19.

16.

Shape Evolution in Neutron-Rich Krypton Isotopes Beyond N=60: First Spectroscopy of ^{98,100}Kr.

Flavigny F, Doornenbal P, Obertelli A, Delaroche JP, Girod M, Libert J, Rodriguez TR, Authelet G, Baba H, Calvet D, Château F, Chen S, Corsi A, Delbart A, Gheller JM, Giganon A, Gillibert A, Lapoux V, Motobayashi T, Niikura M, Paul N, Roussé JY, Sakurai H, Santamaria C, Steppenbeck D, Taniuchi R, Uesaka T, Ando T, Arici T, Blazhev A, Browne F, Bruce A, Carroll R, Chung LX, Cortés ML, Dewald M, Ding B, Franchoo S, Górska M, Gottardo A, Jungclaus A, Lee J, Lettmann M, Linh BD, Liu J, Liu Z, Lizarazo C, Momiyama S, Moschner K, Nagamine S, Nakatsuka N, Nita C, Nobs CR, Olivier L, Orlandi R, Patel Z, Podolyák Z, Rudigier M, Saito T, Shand C, Söderström PA, Stefan I, Vaquero V, Werner V, Wimmer K, Xu Z.

Phys Rev Lett. 2017 Jun 16;118(24):242501. doi: 10.1103/PhysRevLett.118.242501. Epub 2017 Jun 14.

PMID:
28665635
17.

Gamma Decay of Unbound Neutron-Hole States in ^{133}Sn.

Vaquero V, Jungclaus A, Doornenbal P, Wimmer K, Gargano A, Tostevin JA, Chen S, Nácher E, Sahin E, Shiga Y, Steppenbeck D, Taniuchi R, Xu ZY, Ando T, Baba H, Garrote FLB, Franchoo S, Hadynska-Klek K, Kusoglu A, Liu J, Lokotko T, Momiyama S, Motobayashi T, Nagamine S, Nakatsuka N, Niikura M, Orlandi R, Saito T, Sakurai H, Söderström PA, Tveten GM, Vajta Z, Yalcinkaya M.

Phys Rev Lett. 2017 May 19;118(20):202502. doi: 10.1103/PhysRevLett.118.202502. Epub 2017 May 17.

PMID:
28581778
18.

AGO Austria recommendation on screening and diagnosis of Lynch syndrome (LS).

Zeimet AG, Mori H, Petru E, Polterauer S, Reinthaller A, Schauer C, Scholl-Firon T, Singer C, Wimmer K, Zschocke J, Marth C.

Arch Gynecol Obstet. 2017 Jul;296(1):123-127. doi: 10.1007/s00404-017-4392-y. Epub 2017 May 16.

19.

Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis?

Suerink M, Potjer TP, Versluijs AB, Ten Broeke SW, Tops CM, Wimmer K, Nielsen M.

Clin Genet. 2018 Jan;93(1):134-137. doi: 10.1111/cge.13053. Epub 2017 Sep 15.

PMID:
28503822
20.

panelcn.MOPS: Copy-number detection in targeted NGS panel data for clinical diagnostics.

Povysil G, Tzika A, Vogt J, Haunschmid V, Messiaen L, Zschocke J, Klambauer G, Hochreiter S, Wimmer K.

Hum Mutat. 2017 Jul;38(7):889-897. doi: 10.1002/humu.23237. Epub 2017 May 16.

21.

Isomeric Character of the Lowest Observed 4^{+} State in ^{44}S.

Parker JJ, Wiedenhöver I, Cottle PD, Baker J, McPherson D, Riley MA, Santiago-Gonzalez D, Volya A, Bader VM, Baugher T, Bazin D, Gade A, Ginter T, Iwasaki H, Loelius C, Morse C, Recchia F, Smalley D, Stroberg SR, Whitmore K, Weisshaar D, Lemasson A, Crawford HL, Macchiavelli AO, Wimmer K.

Phys Rev Lett. 2017 Feb 3;118(5):052501. doi: 10.1103/PhysRevLett.118.052501. Epub 2017 Jan 31.

PMID:
28211717
22.

Are There Signatures of Harmonic Oscillator Shells Far from Stability? First Spectroscopy of ^{110}Zr.

Paul N, Corsi A, Obertelli A, Doornenbal P, Authelet G, Baba H, Bally B, Bender M, Calvet D, Château F, Chen S, Delaroche JP, Delbart A, Gheller JM, Giganon A, Gillibert A, Girod M, Heenen PH, Lapoux V, Libert J, Motobayashi T, Niikura M, Otsuka T, Rodríguez TR, Roussé JY, Sakurai H, Santamaria C, Shimizu N, Steppenbeck D, Taniuchi R, Togashi T, Tsunoda Y, Uesaka T, Ando T, Arici T, Blazhev A, Browne F, Bruce AM, Carroll R, Chung LX, Cortés ML, Dewald M, Ding B, Flavigny F, Franchoo S, Górska M, Gottardo A, Jungclaus A, Lee J, Lettmann M, Linh BD, Liu J, Liu Z, Lizarazo C, Momiyama S, Moschner K, Nagamine S, Nakatsuka N, Nita C, Nobs CR, Olivier L, Patel Z, Podolyák Z, Rudigier M, Saito T, Shand C, Söderström PA, Stefan I, Orlandi R, Vaquero V, Werner V, Wimmer K, Xu Z.

Phys Rev Lett. 2017 Jan 20;118(3):032501. doi: 10.1103/PhysRevLett.118.032501. Epub 2017 Jan 18.

PMID:
28157341
23.

Two-Proton Radioactivity of ^{67}Kr.

Goigoux T, Ascher P, Blank B, Gerbaux M, Giovinazzo J, Grévy S, Kurtukian Nieto T, Magron C, Doornenbal P, Kiss GG, Nishimura S, Söderström PA, Phong VH, Wu J, Ahn DS, Fukuda N, Inabe N, Kubo T, Kubono S, Sakurai H, Shimizu Y, Sumikama T, Suzuki H, Takeda H, Agramunt J, Algora A, Guadilla V, Montaner-Piza A, Morales AI, Orrigo SE, Rubio B, Fujita Y, Tanaka M, Gelletly W, Aguilera P, Molina F, Diel F, Lubos D, de Angelis G, Napoli D, Borcea C, Boso A, Cakirli RB, Ganioglu E, Chiba J, Nishimura D, Oikawa H, Takei Y, Yagi S, Wimmer K, de France G, Go S, Brown BA.

Phys Rev Lett. 2016 Oct 14;117(16):162501. Epub 2016 Oct 14.

PMID:
27792367
24.

Connections between constitutional mismatch repair deficiency syndrome and neurofibromatosis type 1.

Wimmer K, Rosenbaum T, Messiaen L.

Clin Genet. 2017 Apr;91(4):507-519. doi: 10.1111/cge.12904. Epub 2017 Jan 10. Review.

PMID:
27779754
25.

Impact of Neoadjuvant Chemotherapy on Clinical Risk Scores and Survival in Patients with Colorectal Liver Metastases.

Wimmer K, Schwarz C, Szabo C, Bodingbauer M, Tamandl D, Mittlböck M, Kaczirek K.

Ann Surg Oncol. 2017 Jan;24(1):236-243. doi: 10.1245/s10434-016-5615-3. Epub 2016 Oct 11.

26.

Prefrontal Neurons Represent Motion Signals from Across the Visual Field But for Memory-Guided Comparisons Depend on Neurons Providing These Signals.

Wimmer K, Spinelli P, Pasternak T.

J Neurosci. 2016 Sep 7;36(36):9351-64. doi: 10.1523/JNEUROSCI.0843-16.2016.

27.

Isospin Symmetry at High Spin Studied via Nucleon Knockout from Isomeric States.

Milne SA, Bentley MA, Simpson EC, Baugher T, Bazin D, Berryman JS, Bruce AM, Davies PJ, Diget CA, Gade A, Henry TW, Iwasaki H, Lemasson A, Lenzi SM, McDaniel S, Napoli DR, Nichols AJ, Ratkiewicz A, Scruton L, Stroberg SR, Tostevin JA, Weisshaar D, Wimmer K, Winkler R.

Phys Rev Lett. 2016 Aug 19;117(8):082502. doi: 10.1103/PhysRevLett.117.082502. Epub 2016 Aug 15.

PMID:
27588851
28.

A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency.

Wimmer K, Beilken A, Nustede R, Ripperger T, Lamottke B, Ure B, Steinmann D, Reineke-Plaass T, Lehmann U, Zschocke J, Valle L, Fauth C, Kratz CP.

Fam Cancer. 2017 Jan;16(1):67-71. doi: 10.1007/s10689-016-9925-1.

29.

PMS2 inactivation by a complex rearrangement involving an HERV retroelement and the inverted 100-kb duplicon on 7p22.1.

Vogt J, Wernstedt A, Ripperger T, Pabst B, Zschocke J, Kratz C, Wimmer K.

Eur J Hum Genet. 2016 Nov;24(11):1598-1604. doi: 10.1038/ejhg.2016.75. Epub 2016 Jun 22.

30.

Direct Lifetime Measurements of the Excited States in (72)Ni.

Kolos K, Miller D, Grzywacz R, Iwasaki H, Al-Shudifat M, Bazin D, Bingham CR, Braunroth T, Cerizza G, Gade A, Lemasson A, Liddick SN, Madurga M, Morse C, Portillo M, Rajabali MM, Recchia F, Riedinger LL, Voss P, Walters WB, Weisshaar D, Whitmore K, Wimmer K, Tostevin JA.

Phys Rev Lett. 2016 Mar 25;116(12):122502. doi: 10.1103/PhysRevLett.116.122502. Epub 2016 Mar 22.

PMID:
27058074
31.

Transitions between Multiband Oscillatory Patterns Characterize Memory-Guided Perceptual Decisions in Prefrontal Circuits.

Wimmer K, Ramon M, Pasternak T, Compte A.

J Neurosci. 2016 Jan 13;36(2):489-505. doi: 10.1523/JNEUROSCI.3678-15.2016.

32.

Mass Measurement of 56Sc Reveals a Small A = 56 Odd-Even Mass Staggering, Implying a Cooler Accreted Neutron Star Crust.

Meisel Z, George S, Ahn S, Bazin D, Brown BA, Browne J, Carpino JF, Chung H, Cole AL, Cyburt RH, Estradé A, Famiano M, Gade A, Langer C, Matoš M, Mittig W, Montes F, Morrissey DJ, Pereira J, Schatz H, Schatz J, Scott M, Shapira D, Smith K, Stevens J, Tan W, Tarasov O, Towers S, Wimmer K, Winkelbauer JR, Yurkon J, Zegers RG.

Phys Rev Lett. 2015 Oct 16;115(16):162501. doi: 10.1103/PhysRevLett.115.162501. Epub 2015 Oct 16.

PMID:
26550869
33.

Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity.

Baris HN, Barnes-Kedar I, Toledano H, Halpern M, Hershkovitz D, Lossos A, Lerer I, Peretz T, Kariv R, Cohen S, Half EE, Magal N, Drasinover V, Wimmer K, Goldberg Y, Bercovich D, Levi Z.

Pediatr Blood Cancer. 2016 Mar;63(3):418-27. doi: 10.1002/pbc.25818. Epub 2015 Nov 6.

PMID:
26544533
34.

Decoding NF1 Intragenic Copy-Number Variations.

Hsiao MC, Piotrowski A, Callens T, Fu C, Wimmer K, Claes KB, Messiaen L.

Am J Hum Genet. 2015 Aug 6;97(2):238-49. doi: 10.1016/j.ajhg.2015.06.002. Epub 2015 Jul 16.

35.

Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents.

Bodo S, Colas C, Buhard O, Collura A, Tinat J, Lavoine N, Guilloux A, Chalastanis A, Lafitte P, Coulet F, Buisine MP, Ilencikova D, Ruiz-Ponte C, Kinzel M, Grandjouan S, Brems H, Lejeune S, Blanché H, Wang Q, Caron O, Cabaret O, Svrcek M, Vidaud D, Parfait B, Verloes A, Knappe UJ, Soubrier F, Mortemousque I, Leis A, Auclair-Perrossier J, Frébourg T, Fléjou JF, Entz-Werle N, Leclerc J, Malka D, Cohen-Haguenauer O, Goldberg Y, Gerdes AM, Fedhila F, Mathieu-Dramard M, Hamelin R, Wafaa B, Gauthier-Villars M, Bourdeaut F, Sheridan E, Vasen H, Brugières L, Wimmer K, Muleris M, Duval A; European Consortium “Care for CMMRD”.

Gastroenterology. 2015 Oct;149(4):1017-29.e3. doi: 10.1053/j.gastro.2015.06.013. Epub 2015 Jun 25.

PMID:
26116798
36.

Constitutional or biallelic? Settling on a name for a recessively inherited cancer susceptibility syndrome.

Wimmer K, Brugières L, Duval A, Muleris M, Kratz CP, Vasen HF.

J Med Genet. 2016 Apr;53(4):226. doi: 10.1136/jmedgenet-2015-103249. Epub 2015 Jun 3. No abstract available.

PMID:
26041761
37.

High prevalence of BRCA1 stop mutation c.4183C>T in the Tyrolean population: implications for genetic testing.

Pölsler L, Fiegl H, Wimmer K, Oberaigner W, Amberger A, Traunfellner P, Morscher RJ, Weber I, Fauth C, Wernstedt A, Sperner-Unterweger B, Oberguggenberger A, Hubalek M, Marth C, Zschocke J.

Eur J Hum Genet. 2016 Feb;24(2):258-62. doi: 10.1038/ejhg.2015.108. Epub 2015 May 27.

38.

A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotype.

Li L, Hamel N, Baker K, McGuffin MJ, Couillard M, Gologan A, Marcus VA, Chodirker B, Chudley A, Stefanovici C, Durandy A, Hegele RA, Feng BJ, Goldgar DE, Zhu J, De Rosa M, Gruber SB, Wimmer K, Young B, Chong G, Tischkowitz MD, Foulkes WD.

J Med Genet. 2015 May;52(5):348-52. doi: 10.1136/jmedgenet-2014-102934. Epub 2015 Feb 17.

PMID:
25691505
39.

Sensory integration dynamics in a hierarchical network explains choice probabilities in cortical area MT.

Wimmer K, Compte A, Roxin A, Peixoto D, Renart A, de la Rocha J.

Nat Commun. 2015 Feb 4;6:6177. doi: 10.1038/ncomms7177.

40.

Mass measurements demonstrate a strong N=28 shell gap in argon.

Meisel Z, George S, Ahn S, Browne J, Bazin D, Brown BA, Carpino JF, Chung H, Cyburt RH, Estradé A, Famiano M, Gade A, Langer C, Matoš M, Mittig W, Montes F, Morrissey DJ, Pereira J, Schatz H, Schatz J, Scott M, Shapira D, Smith K, Stevens J, Tan W, Tarasov O, Towers S, Wimmer K, Winkelbauer JR, Yurkon J, Zegers RG.

Phys Rev Lett. 2015 Jan 16;114(2):022501. Epub 2015 Jan 15.

PMID:
25635542
41.

Quadrupole transition strength in the (74)Ni nucleus and core polarization effects in the neutron-rich Ni isotopes.

Marchi T, de Angelis G, Valiente-Dobón JJ, Bader VM, Baugher T, Bazin D, Berryman J, Bonaccorso A, Clark R, Coraggio L, Crawford HL, Doncel M, Farnea E, Gade A, Gadea A, Gargano A, Glasmacher T, Gottardo A, Gramegna F, Itaco N, John PR, Kumar R, Lenzi SM, Lunardi S, McDaniel S, Michelagnoli C, Mengoni D, Modamio V, Napoli DR, Quintana B, Ratkiewicz A, Recchia F, Sahin E, Stroberg R, Weisshaar D, Wimmer K, Winkler R.

Phys Rev Lett. 2014 Oct 31;113(18):182501. Epub 2014 Oct 28.

PMID:
25396363
42.

Somatic neurofibromatosis type 1 (NF1) inactivation events in cutaneous neurofibromas of a single NF1 patient.

Emmerich D, Zemojtel T, Hecht J, Krawitz P, Spielmann M, Kühnisch J, Kobus K, Osswald M, Heinrich V, Berlien P, Müller U, Mautner VF, Wimmer K, Robinson PN, Vingron M, Tinschert S, Mundlos S, Kolanczyk M.

Eur J Hum Genet. 2015 Jun;23(6):870-3. doi: 10.1038/ejhg.2014.210. Epub 2014 Oct 8.

43.

Determining the rp-process flow through 56Ni: resonances in 57Cu(p,γ)58Zn identified with GRETINA.

Langer C, Montes F, Aprahamian A, Bardayan DW, Bazin D, Brown BA, Browne J, Crawford H, Cyburt RH, Domingo-Pardo C, Gade A, George S, Hosmer P, Keek L, Kontos A, Lee IY, Lemasson A, Lunderberg E, Maeda Y, Matos M, Meisel Z, Noji S, Nunes FM, Nystrom A, Perdikakis G, Pereira J, Quinn SJ, Recchia F, Schatz H, Scott M, Siegl K, Simon A, Smith M, Spyrou A, Stevens J, Stroberg SR, Weisshaar D, Wheeler J, Wimmer K, Zegers RG.

Phys Rev Lett. 2014 Jul 18;113(3):032502. Epub 2014 Jul 14.

44.

Neurofibromatosis type 1 (NF1) and associated tumors.

Rosenbaum T, Wimmer K.

Klin Padiatr. 2014 Nov;226(6-7):309-15. doi: 10.1055/s-0034-1382021. Epub 2014 Jul 25. Review.

PMID:
25062113
45.

β+ Gamow-Teller transition strengths from 46Ti and stellar electron-capture rates.

Noji S, Zegers RG, Austin SM, Baugher T, Bazin D, Brown BA, Campbell CM, Cole AL, Doster HJ, Gade A, Guess CJ, Gupta S, Hitt GW, Langer C, Lipschutz S, Lunderberg E, Meharchand R, Meisel Z, Perdikakis G, Pereira J, Recchia F, Schatz H, Scott M, Stroberg SR, Sullivan C, Valdez L, Walz C, Weisshaar D, Williams SJ, Wimmer K.

Phys Rev Lett. 2014 Jun 27;112(25):252501. Epub 2014 Jun 25.

PMID:
25014806
46.

SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints.

Vogt J, Bengesser K, Claes KB, Wimmer K, Mautner VF, van Minkelen R, Legius E, Brems H, Upadhyaya M, Högel J, Lazaro C, Rosenbaum T, Bammert S, Messiaen L, Cooper DN, Kehrer-Sawatzki H.

Genome Biol. 2014 Jun 2;15(6):R80. doi: 10.1186/gb-2014-15-6-r80.

47.

PMS2 gene mutational analysis: direct cDNA sequencing to circumvent pseudogene interference.

Wimmer K, Wernstedt A.

Methods Mol Biol. 2014;1167:289-302. doi: 10.1007/978-1-4939-0835-6_20.

PMID:
24823786
48.

Evolution of collectivity in 72Kr: evidence for rapid shape transition.

Iwasaki H, Lemasson A, Morse C, Dewald A, Braunroth T, Bader VM, Baugher T, Bazin D, Berryman JS, Campbell CM, Gade A, Langer C, Lee IY, Loelius C, Lunderberg E, Recchia F, Smalley D, Stroberg SR, Wadsworth R, Walz C, Weisshaar D, Westerberg A, Whitmore K, Wimmer K.

Phys Rev Lett. 2014 Apr 11;112(14):142502. Epub 2014 Apr 10.

PMID:
24765947
49.

Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD).

Wimmer K, Kratz CP, Vasen HF, Caron O, Colas C, Entz-Werle N, Gerdes AM, Goldberg Y, Ilencikova D, Muleris M, Duval A, Lavoine N, Ruiz-Ponte C, Slavc I, Burkhardt B, Brugieres L; EU-Consortium Care for CMMRD (C4CMMRD).

J Med Genet. 2014 Jun;51(6):355-65. doi: 10.1136/jmedgenet-2014-102284. Epub 2014 Apr 15. Review.

PMID:
24737826
50.

Nuclear structure towards N = 40 60Ca: in-beam γ-ray spectroscopy of 58,60Ti.

Gade A, Janssens RV, Weisshaar D, Brown BA, Lunderberg E, Albers M, Bader VM, Baugher T, Bazin D, Berryman JS, Campbell CM, Carpenter MP, Chiara CJ, Crawford HL, Cromaz M, Garg U, Hoffman CR, Kondev FG, Langer C, Lauritsen T, Lee IY, Lenzi SM, Matta JT, Nowacki F, Recchia F, Sieja K, Stroberg SR, Tostevin JA, Williams SJ, Wimmer K, Zhu S.

Phys Rev Lett. 2014 Mar 21;112(11):112503. Epub 2014 Mar 21.

PMID:
24702356

Supplemental Content

Loading ...
Support Center