logo
科言猫学术研究的AI总结
language
手机端手机端
  • Phone Feature微信小程序
简体中文简体中文
notice消息通知
博客博客
arrow
L

Lina Basel-Salmon

Maccabi Healthcare Services
H指数:15
被引数:1,405

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Global Recommendations for the Use of Diagnostic Genomic Sequencing in the Prenatal Setting on Behalf of the ESHG and ISPD

代表欧洲人类遗传学会（ESHG）和围产期诊断国际学会（ISPD）就产前诊断基因组测序的应用提出全球建议

Prenatal Diagnosis
IF2.7
2026-09-220
OAAI
Zandra C. Deans; Lina Basel Salmon; Kwong Wai Choy; Guido de Wert; Zirui Dong; Lilian Downie; Francesca Romana Grati; Sabine Hentze; Paula Jorge; Brynn Levy; Luca Lovrecic; Dora Mayen; Álvaro Mendes; Michael Morris; Ashley Pritchard; Raquel Gouveia Silva; Tina-Marié Wessels; Francesca Forzano; Natalie J. Chandler
Global recommendations for the use of diagnostic genomic sequencing in the prenatal setting on behalf of the ESHG and ISPD

代表欧洲人类遗传学会（ESHG）和国际产前诊断学会（ISPD）提出的产前诊断基因组测序应用全球建议

European Journal of Human Genetics
IF4.6
2026-09-160
OAAI
Zandra C. Deans; Lina Basel Salmon; Kwong Wai Choy; Guido de Wert; Zirui Dong; Lilian Downie; Francesca Romana Grati; Sabine Hentze; Paula Jorge; Brynn Levy; Luca Lovrecic; Dora Mayen; Álvaro Mendes; Michael Morris; Ashley Pritchard; Raquel Gouveia Silva; Tina-Marié Wessels; Francesca Forzano; Natalie J. Chandler
N-terminal truncating variants in CACNB1 cause a new congenital muscular disorder

CACNB1基因的N端截短变异导致一种新的先天性肌病

European Journal of Human Genetics
IF4.6
2025-09-290
OAAI
Asier Iturrate; Nurit Assia Batzir; Ranit Jaron; David Garcia-Valentin; Julian Nevado; Jair Tenorio-Castano; Pablo Lapunzina; Kamila Lee; Rotem Greenberg; Dvora Sassi; Sharon Aharoni; Alla Kuzminsky; Lina Basel-Salmon; Naama Orenstein; Yakov Fellig; Shay Ben-Shachar; Dina Marek-Yagel; Victor L. Ruiz-Perez
Mono and Biallelic Variants in TRIM63 Are Frequently Associated With a Unique Form of Hypertrophic Cardiomyopathy
CIRCULATION-GENOMIC AND PRECISION MEDICINE
IF5.5
2025-02-010
PRE
Shahar, Noa Ruhrman; Marek-Yagel, Dina; Greenberg, Rotem; Isakov, Ofer; Naftali, Michal; Friedman, Elena; Bazak, Lily; Monakier, Daniel; Veber, Alvit; Shalva, Nechama; Segev, Amitai; Haim, Moti; Sagi-Dain, Lena; Benyamini, Lilach; Shalata, Adel; Josefsberg Ben Yehoshua, Sagi; Basel Salmon, Lina; Hoss, Sara; Ben-Shachar, Shay
Precision Oncology: A Global Perspective on Implementation and Policy Development
JCO GLOBAL ONCOLOGY
IF3
2025-01-010
OA
Horgan, Denis; Tanner, Marcel; Aggarwal, Charu; Thomas, David; Grover, Surbhi; Basel-Salmon, Lina; Dienstmann, Rodrigo; Tan, Tira Jing Ying; Park, Woong-Yang; Abu Rasheed, Hadi Mohamad; Siu, Lillian L.; Ma, Brigette; Ortiz-Lopez, Rocio; van den Bulcke, Marc; Taucher, Silvia Castillo; Ferris, Andrea; Starling, Naureen; Malapelle, Umberto; Longshore, John; Saldana, Hugo Alberto Barrera; Subbiah, Vivek
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
KIDNEY INTERNATIONAL
IF12.6
2024-04-010
OA
Riedhammer, Korbinian M.; Nguyen, Thanh-Minh T.; Kosukcu, Can; Calzada-Wack, Julia; Li, Yong; Batzir, Nurit Assia; Saygili, Seha; Wimmers, Vera; Kim, Gwang-Jin; Chrysanthou, Marialena; Bakey, Zeineb; Sofrin-Drucker, Efrat; Kraiger, Markus; Sanz-Moreno, Adrian; Amarie, Oana V.; Rathkolb, Birgit; Klein-Rodewald, Tanja; Garrett, Lillian; Hoelter, Sabine M.; Seisenberger, Claudia; Haug, Stefan; Schlosser, Pascal; Marschall, Susan; Wurst, Wolfgang; Fuchs, Helmut; Gailus-Durner, Valerie; Wuttke, Matthias; de Angelis, Martin Hrabe; Comic, Jasmina; Dogan, Ozlem Akgun; Ozluk, Yasemin; Tasdemir, Mehmet; Agbas, Ayse; Canpolat, Nur; Orenstein, Naama; Caliskan, Salim; Weber, Ruthild G.; Bergmann, Carsten; Jeanpierre, Cecile; Saunier, Sophie; Lim, Tze Y.; Hildebrandt, Friedhelm; Alhaddad, Bader; Basel-Salmon, Lina; Borovitz, Yael; Wu, Kaman; Antony, Dinu; Matschkal, Julia; Schaaf, Christian W.; Renders, Lutz; Schmaderer, Christoph; Rogg, Manuel; Schell, Christoph; Meitinger, Thomas; Heemann, Uwe; Koettgen, Anna; Arnold, Sebastian J.; Ozaltin, Fatih; Schmidts, Miriam; Hoefele, Julia
A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic features
GENETICS IN MEDICINE
IF6.2
2021-06-0116
OAAI
Shao, Diane D.; Straussberg, Rachel; Ahmed, Hind; Khan, Amjad; Tian, Songhai; Hill, R. Sean; Smith, Richard S.; Majmundar, Amar J.; Ameziane, Najim; Neil, Jennifer E.; Yang, Edward; Al Tenaiji, Amal; Jamuar, Saumya S.; Schlaeger, Thorsten M.; Al-Saffar, Muna; Hovel, Iris; Al-Shamsi, Aisha; Basel-Salmon, Lina; Amir, Achiya Z.; Rento, Lariza M.; Lim, Jiin Ying; Ganesan, Indra; Shril, Shirlee; Evrony, Gilad; Barkovich, A. James; Bauer, Peter; Hildebrandt, Friedhelm; Dong, Min; Borck, Guntram; Beetz, Christian; Al-Gazali, Lihadh; Eyaid, Wafaa; Walsh, Christopher A.

研究方向

暂未获取到该数据
I
Idit Maya
H 指数:22论文数:90被引数:1,498
L
Lena Sagi‐Dain
H 指数:25论文数:175被引数:2,232
Y
Yael Goldberg
H 指数:25论文数:123被引数:2,911
L
Lily Bazak
H 指数:18论文数:63被引数:1,982
D
Dana Brabbing‐Goldstein
H 指数:7论文数:27被引数:200
H 指数:0论文数:43被引数:239
H 指数:0论文数:39被引数:407
R
Rivka Sukenik‐Halevy
H 指数:21论文数:96被引数:1,347
M
Mordechai Shohat
H 指数:33论文数:149被引数:5,058
H 指数:0论文数:25被引数:161