1994-2005年(飯沼教授時代、英文論文のみ)→|2006年(土屋教授就任以後)→|2007年→|2008年→|2009年→|2010年→|2011年(土屋教授退職、呉教授就任)→|2012年→|2013年→|2014年→|2015年→|2016年→|2017年→|2018年→|2019年→|2020年→|2021→|2022→|
2021
【1月】
Hozawa A‚ Tanno K‚ Nakaya N‚ Nakamura T‚ Tsuchiya N‚ Hirata T‚ Narita A‚ Kogure M‚ Nochioka K‚ Sasaki R‚ Takanashi N‚ Otsuka K‚ Sakata K‚ Kuriyama S‚ Kikuya M‚ Tanabe O‚ Sugawara J‚ Suzuki K‚ Suzuki Y‚ Kodama EN‚ Fuse N‚ Kiyomoto H‚ Tomita H‚ Uruno A‚ Hamanaka Y‚ Metoki H‚ Ishikuro M‚ Obara T‚ Kobayashi T‚ Kitatani K‚ Takai-Igarashi T‚ Ogishima S‚ Satoh M‚ Ohmomo H‚ Tsuboi A‚ Egawa S‚ Ishii T‚ Ito K‚ Ito S‚ Taki Y‚ Minegishi N‚ Ishii N‚ Nagasaki M‚ Igarashi K‚ Koshiba S‚ Shimizu R‚ Tamiya G‚ Nakayama K‚ Motohashi H‚ Yasuda J‚ Shimizu A‚ Hachiya T‚ Shiwa Y‚ Tominaga T‚ Tanaka H‚ Oyama K‚ Tanaka R‚ Kawame H‚ Fukushima A‚ Ishigaki Y‚ Tokutomi T‚ Osumi N‚ Kobayashi T‚ Nagami F‚ Hashizume H‚ Arai T‚ Kawaguchi Y‚ Higuchi S‚ Sakaida M‚ Endo R‚ Nishizuka S‚ Tsuji I‚ Hitomi J‚ Nakamura M‚ Ogasawara K‚ Yaegashi N‚ Kinoshita K‚ Kure S‚ Sakai A‚ Kobayashi S‚ Sobue K‚ Sasaki M‚ Yamamoto M.
Study profile of The Tohoku Medical Megabank Community-Based Cohort Study.
J Epidemiol. 31:65-76‚ 2021
Nagaoka S‚ Yamaguchi-Kabata Y‚ Shiga N‚ Tachibana M‚ Yasuda J‚ Tadaka S‚ Tamiya G‚ Fuse N‚ Kinoshita K‚ Kure S‚ Murotsuki J‚ Yamamoto M‚ Yaegashi N‚ Sugawara J.
Estimation of the carrier frequencies and proportions of potential patients by detecting causative gene variants associated with autosomal recessive bone dysplasia using a whole-genome reference panel of Japanese individuals.
Hum Genome Var. 8:2‚ 2021
Saito S‚ Aoki Y‚ Tamahara T‚ Goto M‚ Matsui H‚ Kawashima J‚ Danjoh I‚ Hozawa A‚ Kuriyama S‚ Suzuki Y‚ Fuse N‚ Kure S‚ Yamashita R‚ Tanabe O‚ Minegishi N‚ Kinoshita K‚ Tsuboi A‚ Shimizu R‚ Yamamoto M.
Oral Microbiome Analysis in Prospective Genome Cohort Studies of the Tohoku Medical Megabank Project.
Front Cell Infect Microbiol. 10:604596‚ 2021
【2月】
Iwafuchi S‚ Kikuchi A‚ Endo W‚ Inui T‚ Aihara Y‚ Satou K‚ Kaname T‚ Kure S.
A novel stop-gain CUL3 mutation in a Japanese patient with autism spectrum disorder.
Brain Dev. 43:303-307‚ 2021
Ishii T‚ Kushimoto S‚ Katori Y‚ Kure S‚ Igarashi K‚ Fujita M‚ Takayama S‚ Abe M‚ Tanaka J‚ Kikuchi A‚ Abe Y‚ Imai H‚ Inaba Y‚ Iwamatsu-Kobayashi Y‚ Nishioka T‚ Onodera K‚ Akaishi T.
Predictors of SARS-CoV-2 Positivity Based on RT-PCR Swab Tests at a Drive-Through Outpatient Clinic for COVID-19 Screening in Japan.
Tohoku J Exp Med. 253:101-108‚ 2021
Abe Y‚ Aihara Y‚ Endo W‚ Hasegawa H‚ Ichida K‚ Uematsu M‚ Kure S.
The effect of dietary protein restriction in a case of molybdenum cofactor deficiency with MOCS1 mutation.
Mol Genet Metab Rep. 26:100716‚ 2021
【4月】
Kobayashi M‚ Watanabe S‚ Matsuda T‚ Ikeda H‚ Nawa T‚ Sato S‚ Usuda H‚ Hanita T‚ Kobayashi Y.
Diagnostic Specificity of Cerebral Magnetic Resonance Imaging for Punctate White Matter Lesion Assessment in a Preterm Sheep Fetus Model.
Reprod Sci. 28:1175-1184‚ 2021
Totsune E‚ Nakano T‚ Moriya K‚ Sato D‚ Suzuki D‚ Miura A‚ Katayama S‚ Niizuma H‚ Kanno J‚ van Zelm MC‚ Imai K‚ Kanegane H‚ Sasahara Y‚ Kure S.
Case Report: Infantile-Onset Fulminant Type 1 Diabetes Mellitus Caused by Novel Compound Heterozygous LRBA Variants.
Front Immunol. 12:677572‚ 2021
Nagasaki K‚ Nakamura A‚ Yamauchi T‚ Kamasaki H‚ Hara Y‚ Kanno J‚ Koyama S‚ Ohtsu Y‚ Takahashi I‚ Suzuki S‚ Kashimada K‚ Tajima T.
Investigation of TSH receptor blocking antibodies in childhood-onset atrophic autoimmune thyroiditis.
Clin Pediatr Endocrinol. 30(2):79-84‚ 2021
Oikawa T‚ Ota C‚ Iwasawa S‚ Onoki T‚ Ikeda H‚ Hanita T.
Thoracic Empyema Secondary to Congenital Chylothorax in a 14-Month-Old Boy with Noonan Syndrome.
Case Reports in Pediatrics. Article ID 6620353‚ 2021
【5月】
Izumi T‚ Aihara Y‚ Kikuchi A‚ Kure S.
Electroencephalographic findings and genetic characterization of two brothers with IQSEC2 pathogenic variant.
Brain Dev. 43:652-656‚ 2021
Yashima K‚ Obara T‚ Matsuzaki F‚ Suzuki C‚ Saeki M‚ Koyama M‚ Hosono M‚ Noda A‚ Kikuchi S‚ Hoshiai T‚ Sato S‚ Saito M‚ Hanita T‚ Mano N.
Evaluation of the Safety of Taking Lamotrigine During Lactation Period.
Breastfeed Med. 16:432-438‚ 2021
【6月】
Kuroda K‚ Moriya K‚ Nakano T‚ Saito R‚ Sato D‚ Katayama S‚ Niizuma H‚ Watanuki M‚ Uematsu M‚ Sasahara Y‚ Kure S.
A pediatric case of osteosarcoma and tuberous sclerosis complex with a novel germline mutation in the TSC2 gene and a somatic mutation in the TP53 gene.
Pediatr Blood Cancer. 68(6):e28960‚ 2021
Akaishi T‚ Kushimoto S‚ Katori Y‚ Kure S‚ Igarashi K‚ Takayama S‚ Abe M‚ Tanaka J‚ Kikuchi A‚ Onodera K‚ Ishii T.
COVID-19 transmission in group living environments and households.
Sci Rep. 11:11616‚ 2021
Kawashima S‚ Hattori A‚ Suzuki E‚ Matsubara K‚ Toki M‚ Kosaki R‚ Hasegawa Y‚ Nakabayashi K‚ Fukami M‚ Kagami M.
Methylation status of genes escaping from X-chromosome inactivation in patients with X-chromosome rearrangements.
Clin Epigenetics. 13:134‚ 2021
【7月】
Hirata T‚ Kogure M‚ Tsuchiya N‚ Miyagawa K‚ Narita A‚ Nochioka K‚ Uruno A‚ Obara T‚ Nakamura T‚ Nakaya N‚ Metoki H‚ Kikuya M‚ Sugawara J‚ Kuriyama S‚ Tsuji I‚ Kure S‚ Hozawa A.
Impacts of the urinary sodium-to-potassium ratio‚ sleep efficiency‚ and conventional risk factors on home hypertension in a general Japanese population.
Hypertens Res. 44:858-865‚ 2021.
Nakagawa T‚ Wada Y‚ Miura A‚ Numata-Uematsu Y‚ Niizuma H‚ Kure S.
Gingival pigmentation in a boy.
J Pediatr. 234:274-275‚ 2021
Fukui R‚ Hidaka T‚ Terui H‚ Rikiishi T‚ Sasahara Y‚ Kagimoto Y‚ Kusakari Y‚ Yamasaki K‚ Aiba S.
Chronological changes of skin eruptions toward cold abscess formation in hyper-immunoglobulin E syndrome.
J Dermatol. 48(7):e316-e317.
Ishii T‚ Kushimoto S‚ Katori Y‚ Kure S‚ Igarashi K‚ Fujita M‚ Sugawara N‚ Takayama S‚ Abe M‚ Tanaka J‚ Kikuchi A‚ Abe Y‚ Imai H‚ Inaba Y‚ Iwamatsu-Kobayashi Y‚ Nishioka T‚ Onodera K‚ Akaishi T.
Impacts of Natural Environmental Factors and Prevalence of Airway Symptoms on the Local Spread of COVID-19: A Time-Series Analysis in Regional COVID-19 Epidemics.
Tohoku J Exp Med. 254:89-100‚ 2021
Kido J‚ Matsumoto S‚ Häberle J‚ Nakajima Y‚ Wada Y‚ Mochizuki N‚ Murayama K‚ Lee T‚ Mochizuki H‚ Watanabe Y‚ Horikawa R‚ Kasahara M‚ Nakamura K.
Long-term outcome of urea cycle disorders: Report from a nationwide study in Japan.
J Inherit Metab Dis. 44:826-837‚ 2021
Arai-Ichinoi N‚ Kikuchi A‚ Wada Y‚ Sakamoto O‚ Kure S.
Hypoglycemic attacks and growth failure are the most common manifestations of citrin deficiency after 1 year of age.
J Inherit Metab Dis. 44:838-846‚ 2021
【8月】
Niizuma H‚ Searleman AC‚ Takeda S‚ Armstrong SA‚ Park CY‚ Cheng EH‚ Hsieh JJ.
Taspase1 orchestrates fetal liver hematopoietic stem cell and vertebrae fates by cleaving TFIIA.
JCI Insight. 6:149382‚ 2021
【9月】
Terui H‚ Yamasaki K‚ Hagiwara-Takita A‚ Shimada-Omori R‚ Tsuchiyama K‚ Saito-Nanjo Y‚ Rikiishi T‚ Sasahara Y‚ Aiba S.
Pediatric psoriasis induced by HLA-B46-Cw1 haplotype: A retrospective study of psoriasis onset after hematopoietic stem cell transplantation.
J Dermatol. 48:1381-1385‚ 2021
Numata-Uematsu Y‚ Uematsu M‚ Yamamoto T‚ Saitsu H‚ Katata Y‚ Oikawa Y‚ Saijyo N‚ Inui T‚ Murayama K‚ Ohtake A‚ Osaka H‚ Takanashi JI‚ Kure S‚ Inoue K.
Leigh syndrome-like MRI changes in a patient with biallelic HPDL variants treated with ketogenic diet.
Mol Genet Metab Rep. 29:100800‚ 2021
Takahashi Y‚ Saito M‚ Usuda H‚ Takahashi T‚ Watanabe S‚ Hanita T‚ Sato S‚ Kumagai Y‚ Koshinami S‚ Ikeda H‚ Carter S‚ Fee EL‚ Furfaro L‚ Chemtob S‚ Keelan J‚ Olson D‚ Yaegashi N‚ Newnham JP‚ Jobe AH‚ Kemp MW.
Direct administration of the non-competitive interleukin-1 receptor antagonist rytvela transiently reduced intrauterine inflammation in an extremely preterm sheep model of chorioamnionitis.
PLoS One. 16:e0257847‚ 2021
Akaishi T‚ Kushimoto S‚ Katori Y‚ Kure S‚ Igarashi K‚ Fujita M‚ Takayama S‚ Abe M‚ Kikuchi A‚ Tanaka J‚ Abe Y‚ Imai H‚ Inaba Y‚ Iwamatsu-Kobayashi Y‚ Nishioka T‚ Onodera K‚ Ishii T.
Discriminatory Value of Self-reported Olfactory Dysfunction in the Prediction of Coronavirus Disease 2019.
Intern Med. 60:2905-2910‚ 2021
【10月】
Ota C‚ Saito R‚ Tominaga J‚ Iwasawa S‚ Hirama T‚ Matsuda Y‚ Ono K‚ Onoki T‚ Kimura M‚ Kawabata Y‚ Okada Y.
Bilateral lung transplantation in a 9-year-old girl with bronchopulmonary dysplasia with pulmonary hypertension.
Pediatr Pulmonol. 56:3417-3421‚ 2021
Kikuchi A‚ Wada Y‚ Ohura T‚ Kure S.
The Discovery of GALM Deficiency (Type IV Galactosemia) and Newborn Screening System for Galactosemia in Japan.
Int J Neonatal Screen. 7:68‚ 2021
Takase M‚ Nakamura T‚ Tsuchiya N‚ Kogure M‚ Itabashi F‚ Narita A‚ Hirata T‚ Nakaya N‚ Hamanaka Y‚ Sugawara J‚ Suzuki K‚ Fuse N‚ Uruno A‚ Kodama EN‚ Kuriyama S‚ Tsuji I‚ Kure S‚ Hozawa A.
Association between the combined fat mass and fat-free mass index and hypertension: The Tohoku Medical Megabank Community-based Cohort Study.
Clin Exp Hypertens. 43:610-621‚ 2021
Hong J‚ Yun HJ‚ Park G‚ Kim S‚ Ou Y‚ Vasung L‚ Rollins CK‚ Ortinau CM‚ Takeoka E‚ Akiyama S‚ Tarui T‚ Estroff JA‚ Grant PE‚ Lee JM‚ Im K.
Optimal Method for Fetal Brain Age Prediction Using Multiplanar Slices From Structural Magnetic Resonance Imagingv.
Front Neurosci. 15:714252‚ 2021
Tashiro R‚ Niizuma K‚ Kasamatsu J‚ Okuyama Y‚ Rashad S‚ Kikuchi A‚ Fujimura M‚ Kure S‚ Ishii N‚ Tominaga T.
Dysregulation of Rnf 213 gene contributes to T cell response via antigen uptake‚ processing‚ and presentation.
J Cell Physiol. 236:7554-7564‚ 2021
Numata-Uematsu Y‚ Uematsu M‚ Sakuraba R‚ Iwasaki M‚ Osawa S‚ Jin K‚ Nakasato N‚ Kure S.
The Onset of Interictal Spike-Related Ripples Facilitates Detection of the Epileptogenic Zone.
Front Neurol. 12:724417‚ 2021
Sato D‚ Moriya K‚ Nakano T‚ Miyagawa C‚ Katayama S‚ Niizuma H‚ Sasahara Y‚ Kure S.
Refractory T-cell/histiocyte-rich large B-cell lymphoma in a patient with ataxia-telangiectasia caused by novel compound heterozygous variants in ATM.
Int J Hematol. 114:735-741‚ 2021
Nishimoto Y‚ Tsubono Y‚ Kogure M‚ Nakamura T‚ Itabashi F‚ Tsuchiya N‚ Nakaya N‚ Tanno K‚ Sugawara J‚ Kuriyama S‚ Kure S‚ Tsuji I‚ Hozawa A.
The prevalence of current smokers and alcohol drinkers among cancer survivors and subjects with no history of cancer among participants in a community-based cardiometabolic screening program in Miyagi prefecture‚ Japan: a comparison with nationally representative surveys in other countries.
Cancer Med. 10:9000-9011‚ 2021
Hagiwara M‚ Niizuma H‚ Kazama T‚ Sasahara Y‚ Kure S.
Catecholamine-induced paralytic ileus controlled by phentolamine in a child with giant differentiating neuroblastoma.
Pediatr Blood Cancer. 68(12):e29266.
Ogishima S‚ Nagaie S‚ Mizuno S‚ Ishiwata R‚ Iida K‚ Shimokawa K‚ Takai-Igarashi T‚ Nakamura N‚ Nagase S‚ Nakamura T‚ Tsuchiya N‚ Nakaya N‚ Murakami K‚ Ueno F‚ Onuma T‚ Ishikuro M‚ Obara T‚ Mugikura S‚ Tomita H‚ Uruno A‚ Kobayashi T‚ Tsuboi A‚ Tadaka S‚ Katsuoka F‚ Narita A‚ Sakurai M‚ Makino S‚ Tamiya G‚ Aoki Y‚ Shimizu R‚ Motoike IN‚ Koshiba S‚ Minegishi N‚ Kumada K‚ Nobukuni T‚ Suzuki K‚ Danjoh I‚ Nagami F‚ Tanno K‚ Ohmomo H‚ Asahi K‚ Shimizu A‚ Hozawa A‚ Kuriyama S; Tohoku Medical Megabank Project Study Group‚ Fuse N‚ Tominaga T‚ Kure S‚ Yaegashi N‚ Kinoshita K‚ Sasaki M‚ Tanaka H‚ Yamamoto M.
dbTMM: an integrated database of large-scale cohort‚ genome and clinical data for the Tohoku Medical Megabank Project.
Hum Genome Var. 8:44‚ 2021
Suzuki T‚ Wada Y‚ Mikami-Saito Y‚ Kikuchi A‚ Kure S.
Usefulness of serum BUN or BUN/creatinine ratio as markers for citrin deficiency in positive cases of newborn screening.
Mol Genet Metab Rep. 30:100834‚ 2021
甲田一馬、赤荻茉莉子、関谷博顕、大塚喜久、米田行宏、菊池敦生、呉繁夫、影山恭史
福祉施設入所を契機に発症し中鎖脂肪酸オイルが有効であった成人発症II型シトルリン血症の1例
臨床神経 61:200-203‚ 2021
川嶋有朋、 福與なおみ、 阿部裕、 竹澤祐介、 植松貢、 植松有里佳、 高橋利幸、 西山修平、 中島一郎、 呉繁夫
抗AQP4抗体が再陽転化し再発した視神経脊髄炎関連疾患の小児例
脳と発達 53:66-68‚ 2021
佐藤大二郎,大田千晴,六郷由佳,大軒健彦,岩澤伸哉,木村正人
川崎病冠動脈病変における小瘤形成例と中等・巨大瘤形成例の臨床的相違
日本小児救急医学会雑誌 20:423-431‚ 2021
和田陽一
低血糖
小児科診療 84:213-218‚ 2021
呉繁夫、田中総一郎 
災害に対する小児医療システム
小児科診療 84:329-334‚ 2021
植松有里佳
大脳白質形成不全症の疾患モデル細胞を用いた病態解明
脳と発達 53:264-268‚ 2021
和田陽一
ガラクトース血症
遺伝子医学 11:61-65‚ 2021
笹原洋二
先天性血小板減少症・異常症
臨床血液 62:1319-1326‚ 2021
笹原洋二、國島伸治、石黒精、日本小児血液・がん学会血小板委員会
先天性血小板減少症・異常症の診療ガイド
日本小児血液・がん学会雑誌 58:253-262‚ 2021
笹原洋二
「クリニカルガイド小児科—専門医の診断・治療—」南山堂
血小板減少 p728-733
笹原洋二
「新臨床腫瘍学(改訂第6版)」南江堂
横紋筋肉腫 p564-566
植松有里佳
「画像で診る遺伝性白質疾患 診断の手引き」診断と治療社
フェニルケトン尿症 p80-81
和田陽一
「小児救命救急・ICUピックアップ⑤ 内分泌・代謝救急疾患」メディカル・サイエンス・インターナショナル
血糖、血液ガス分析、アンモニア p73-80
菅野潤子
「小児がん内分泌診療の手引き」診断と治療社
副腎異常 p87-90
菅野潤子
「小児がん内分泌診療の手引き」診断と治療社
骨カルシウム代謝異常 p115-119
笹原洋二
「小児内科2021年53巻増刊号 小児疾患診療のための病態生理2 改訂第6版」東京医学社
複合免疫不全症 p695-701
竹澤祐介:2021年米国てんかん学会
奨励賞(ポスドク研究部門)
「Calcium overload and cell swelling during hypoxia in the neonatal brain.」
菊池敦生:日本人類遺伝学会第66回大会
奨励賞
「新規希少遺伝性疾患の概念確立」
阿部裕:第22回乳幼児けいれん研究会国際シンポジウム(台湾)
ISS Research Award
「The Effect of Dietary Protein Restriction in a Case of Molybdenum Cofactor Deficiency」