Thomas B Friedman (Thomas Friedman)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 27

Top Venues

National Institutes of Health Office of History

University of Michigan (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

National Institutes of Health Office of History

United States

Laboratory Chief :: NIDCD, Laboratory of Molecular Genetics

Education History

University of Michigan

United States

PHD :: Zoology

Publications

Takushi Miyoshi, Harshad Vishwasrao, Inna Belyantseva, Mrudhula Sajeevadathan, Yasuko Ishibashi, Samuel Adadey, Narinobu Harada, Hari Shroff, Thomas B Friedman
Live-cell single-molecule fluorescence microscopy for protruding organelles reveals regulatory mechanisms of MYO7A-driven cargo transport in stereocilia of inner ear hair cells. Research square (2024)
Rabia Faridi, Pamela Stratton, Noemi Salmeri, Robert J Morell, Asma Ali Khan, Muhammad A Usmani, William G Newman, Sheikh Riazuddin, Thomas B Friedman
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome. Clinical genetics 105 (5) (2024)
Takushi Miyoshi, Harshad Vishwasrao, Inna Belyantseva, Mrudhula Sajeevadathan, Yasuko Ishibashi, Samuel Adadey, Narinobu Harada, Hari Shroff, Thomas B Friedman
Live-cell single-molecule fluorescence microscopy for protruding organelles reveals regulatory mechanisms of MYO7A-driven cargo transport in stereocilia of inner ear hair cells. Research square (2024)
Rabia Faridi, Rizwan Yousaf, Sayaka Inagaki, Rafal Olszewski, Shoujun Gu, Robert J Morell, Elizabeth Wilson, Ying Xia, Tanveer Ahmed Qaiser, Muhammad Rashid, Cristina Fenollar-Ferrer, Michael Hoa, Sheikh Riazuddin, Thomas B Friedman
Deafness DFNB128 Associated with a Recessive Variant of Human MAP3K1 Recapitulates Hearing Loss of Map3k1 -Deficient Mice. Genes 15 (7) (2024)
Rabia Faridi, Rizwan Yousaf, Sayaka Inagaki, Rafal Olszewski, Shoujun Gu, Robert J Morell, Elizabeth Wilson, Ying Xia, Tanveer Ahmed Qaiser, Muhammad Rashid, Cristina Fenollar-Ferrer, Michael Hoa, Sheikh Riazuddin, Thomas B Friedman
Deafness DFNB128 Associated with a Recessive Variant of Human MAP3K1 Recapitulates Hearing Loss of Map3k1 -Deficient Mice. Genes 15 (7) (2024)
Rabia Faridi, Pamela Stratton, Noemi Salmeri, Robert J Morell, Asma Ali Khan, Muhammad A Usmani, William G Newman, Sheikh Riazuddin, Thomas B Friedman
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome. Clinical genetics (2024)
Rabia Faridi, Pamela Stratton, Noemi Salmeri, Robert J Morell, Asma Ali Khan, Muhammad A Usmani, William G Newman, Sheikh Riazuddin, Thomas B Friedman
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome. Clinical genetics 105 (5) (2024)
Takushi Miyoshi, Harshad Vishwasrao, Inna Belyantseva, Mrudhula Sajeevadathan, Yasuko Ishibashi, Samuel Adadey, Narinobu Harada, Hari Shroff, Thomas B Friedman
Live-cell single-molecule fluorescence microscopy for protruding organelles reveals regulatory mechanisms of MYO7A-driven cargo transport in stereocilia of inner ear hair cells. Research square (2024)
Rabia Faridi, Pamela Stratton, Noemi Salmeri, Robert J Morell, Asma Ali Khan, Muhammad A Usmani, William G Newman, Sheikh Riazuddin, Thomas B Friedman
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome. Clinical genetics 105 (5) (2024)
Rabia Faridi, Rizwan Yousaf, Sayaka Inagaki, Rafal Olszewski, Shoujun Gu, Robert J Morell, Elizabeth Wilson, Ying Xia, Tanveer Ahmed Qaiser, Muhammad Rashid, Cristina Fenollar-Ferrer, Michael Hoa, Sheikh Riazuddin, Thomas B Friedman
Deafness DFNB128 Associated with a Recessive Variant of Human MAP3K1 Recapitulates Hearing Loss of Map3k1 -Deficient Mice. Genes 15 (7) (2024)
Rabia Faridi, Rizwan Yousaf, Sayaka Inagaki, Rafal Olszewski, Shoujun Gu, Robert J Morell, Elizabeth Wilson, Ying Xia, Tanveer Ahmed Qaiser, Muhammad Rashid, Cristina Fenollar-Ferrer, Michael Hoa, Sheikh Riazuddin, Thomas B Friedman
Deafness DFNB128 Associated with a Recessive Variant of Human MAP3K1 Recapitulates Hearing Loss of Map3k1 -Deficient Mice. Genes 15 (7) (2024)
Rabia Faridi, Pamela Stratton, Noemi Salmeri, Robert J Morell, Asma Ali Khan, Muhammad A Usmani, William G Newman, Sheikh Riazuddin, Thomas B Friedman
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome. Clinical genetics 105 (5) (2024)
Takushi Miyoshi, Harshad Vishwasrao, Inna Belyantseva, Mrudhula Sajeevadathan, Yasuko Ishibashi, Samuel Adadey, Narinobu Harada, Hari Shroff, Thomas B Friedman
Live-cell single-molecule fluorescence microscopy for protruding organelles reveals regulatory mechanisms of MYO7A-driven cargo transport in stereocilia of inner ear hair cells. Research square (2024)
Rabia Faridi, Pamela Stratton, Noemi Salmeri, Robert J Morell, Asma Ali Khan, Muhammad A Usmani, William G Newman, Sheikh Riazuddin, Thomas B Friedman
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome. Clinical genetics 105 (5) (2024)
Rabia Faridi, Rizwan Yousaf, Shoujun Gu, Sayaka Inagaki, Amy E Turriff, Keith Pelstring, Bin Guan, Amelia Naik, Andrew J Griffith, Samuel Mawuli Adadey, Elvis Twumasi Aboagye, Gordon Akanzuwine Awandare, Robert J Morell, Ekaterini Tsilou, Amanda G Noyes, Laura Anne Goodell Sulmonte, Ambroise Wonkam, Isabelle Schrauwen, Regie Lyn P Santos-Cortez, Hela Azaiez, Carmen C Brewer, Sheikh Riazuddin, Robert B Hufnagel, Michael Hoa, Wadih M Zein, J Karl de Dios, Thomas B Friedman
Variants of LRP2, encoding a multifunctional cell-surface endocytic receptor, associated with hearing loss and retinal dystrophy. Clinical genetics (2023)
Hesam Babahosseini, Inna A Belyantseva, Rizwan Yousaf, Risa Tona, Shadan Hadi, Sayaka Inagaki, Elizabeth Wilson, Shin-Ichiro Kitajiri, Gregory I Frolenkov, Thomas B Friedman, Alexander X Cartagena-Rivera
Unbalanced bidirectional radial stiffness gradients within the organ of Corti promoted by TRIOBP. Proceedings of the National Academy of Sciences of the United States of America 119 (26) (2022)
Jocelyn F Krey, Chang Liu, Inna A Belyantseva, Michael Bateschell, Rachel A Dumont, Jennifer Goldsmith, Paroma Chatterjee, Rachel S Morrill, Lev M Fedorov, Sarah Foster, Jinkyung Kim, Alfred L Nuttall, Sherri M Jones, Dongseok Choi, Thomas B Friedman, Anthony J Ricci, Bo Zhao, Peter G Barr-Gillespie
ANKRD24 organizes TRIOBP to reinforce stereocilia insertion points. The Journal of cell biology 221 (4) (2022)
Saumil Sethna, Wadih M Zein, Sehar Riaz, Arnaud Pj Giese, Julie M Schultz, Todd Duncan, Robert B Hufnagel, Carmen C Brewer, Andrew J Griffith, T Michael Redmond, Saima Riazuddin, Thomas B Friedman, Zubair M Ahmed
Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndrome. eLife 10 (2021)
Adebolajo A Adeyemo, Rabia Faridi, Parna Chattaraj, Rizwan Yousaf, Risa Tona, Samuel Okorie, Thashi Bharadwaj, Liz M Nouel-Saied, Anushree Acharya, Isabelle Schrauwen, Robert J Morell, Regie Lyn P Santos-Cortez, Thomas B Friedman, Andrew J Griffith, Isabelle Roux
Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria. European journal of human genetics : EJHG (2021)
Rabia Faridi, Alessandro Rea, Cristina Fenollar-Ferrer, Raymond T O'Keefe, Shoujun Gu, Zunaira Munir, Asma Ali Khan, Sheikh Riazuddin, Michael Hoa, Sadaf Naz, William G Newman, Thomas B Friedman
New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder. Human genetics (2021)
Memoona Ramzan, Christophe Philippe, Inna A Belyantseva, Yoko Nakano, Cristina Fenollar-Ferrer, Risa Tona, Rizwan Yousaf, Rasheeda Bashir, Ayesha Imtiaz, Rabia Faridi, Zunaira Munir, Hafiza Idrees, Midhat Salman, Sophie Nambot, Antonio Vitobello, Souad Kartti, Oumaima Zarrik, P Dane Witmer, Nara Lygia de Macena Sobreira, Azeddine Ibrahimi, Botond Banfi, Sebastien Moutton, Thomas B Friedman, Sadaf Naz
Variants of human CLDN9 cause mild to profound hearing loss. Human mutation 42 (10) (2021)
Rosalie M Nolen, Robert B Hufnagel, Thomas B Friedman, Amy E Turriff, Carmen C Brewer, Christopher K Zalewski, Kelly A King, Talah T Wafa, Andrew J Griffith, Brian P Brooks, Wadih M Zein
Atypical and ultra-rare Usher syndrome: a review. Ophthalmic genetics 41 (5) (2020)
Risa Tona, Ivan A Lopez, Cristina Fenollar-Ferrer, Rabia Faridi, Claudio Anselmi, Asma A Khan, Mohsin Shahzad, Robert J Morell, Shoujun Gu, Michael Hoa, Lijin Dong, Akira Ishiyama, Inna A Belyantseva, Sheikh Riazuddin, Thomas B Friedman
Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness. Genes 11 (10) (2020)
Sadaf Naz, Thomas B Friedman
Growth factor and receptor malfunctions associated with human genetic deafness. Clinical genetics 97 (1) (2019)
Luca Melli, Neil Billington, Sara A Sun, Jonathan E Bird, Attila Nagy, Thomas B Friedman, Yasuharu Takagi, James R Sellers
Bipolar filaments of human nonmuscle myosin 2-A and 2-B have distinct motile and mechanical properties. eLife 7 (2018)
Elodie M Richard, Regie Lyn P Santos-Cortez, Rabia Faridi, Atteeq U Rehman, Kwanghyuk Lee, Mohsin Shahzad, Anushree Acharya, Asma A Khan, Ayesha Imtiaz, Imen Chakchouk, Christina Takla, Izoduwa Abbe, Maria Rafeeq, Khurram Liaqat, Taimur Chaudhry, Michael J Bamshad, Deborah A Nickerson, null null, Isabelle Schrauwen, Shaheen N Khan, Robert J Morell, Saba Zafar, Muhammad Ansar, Zubair M Ahmed, Wasim Ahmad, Sheikh Riazuddin, Thomas B Friedman, Regie Lyn P Santos-Cortez, Saima Riazuddin
Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss. Human mutation 40 (1) (2018)
Rabia Faridi, Risa Tona, Alessandra Brofferio, Michael Hoa, Rafal Olszewski, Isabelle Schrauwen, Muhammad Z K Assir, Akhtar A Bandesha, Asma A Khan, Atteeq U Rehman, Carmen C Brewer, Wasim Ahmed, Suzanne M Leal, Sheikh Riazuddin, Steven E Boyden, Thomas B Friedman
Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange-Nielsen Syndrome and Romano-Ward Syndrome. Human mutation 40 (2) (2018)

Thomas B Friedman.css-eqlu8i{font-size:small;padding-left:4px;} (Thomas Friedman)

Publication Activity (10 Years)

Top Topics

Top Venues

Thomas B Friedman (Thomas Friedman)